Skip to content
naulon
Get started

No retraction, correction or concern found when last checked on Oct 24, 2026.

Skin Pigmentation Types, Causes and Treatment—A Review

Amin Mahmood Thawabteh, Alaa Jibreen, Donia Karaman and 2 more

Molecules · 2023 · Review · CC BY

doi:10.3390/molecules28124839

Abstract

Human skin pigmentation and melanin synthesis are incredibly variable, and are impacted by genetics, UV exposure, and some drugs. Patients’ physical appearance, psychological health, and social functioning are all impacted by a sizable number of skin conditions that cause pigmentary abnormalities. Hyperpigmentation, where pigment appears to overflow, and hypopigmentation, where pigment is reduced, are the two major classifications of skin pigmentation. Albinism, melasma, vitiligo, Addison’s disease, and post-inflammatory hyperpigmentation, which can be brought on by eczema, acne vulgaris, and drug interactions, are the most common skin pigmentation disorders in clinical practice. Anti-inflammatory medications, antioxidants, and medications that inhibit tyrosinase, which prevents the production of melanin, are all possible treatments for pigmentation problems. Skin pigmentation can be treated orally and topically with medications, herbal remedies, and cosmetic products, but a doctor should always be consulted before beginning any new medicine or treatment plan. This review article explores the numerous types of pigmentation problems, their causes, and treatments, as well as the 25 plants, 4 marine species, and 17 topical and oral medications now on the market that have been clinically tested to treat skin diseases.

Full text

From PubMed Central, U.S. National Library of Medicine, as current on Oct 24, 2026. Paragraph numbers are ours, so an answer can point at one.

1. Introduction

Skin pigmentation, which refers to how much melanin the body generates, determines the color of the skin. The two main types of melanin, eumelanin, and pheomelanin, are produced by melanocytes in the epidermal layer of the skin. Pheomelanin causes lighter skin tones, while eumelanin is responsible for darker skin tones.

The skin is protected from sunburn by the dark brown pigment eumelanin (compound 1 in Figure 1), which absorbs UV rays from the sun. Darker skin tones are related to higher levels of eumelanin, while lighter skin tones are associated with lower levels. The capacity of eumelanin to prevent skin cancer is one of its additional benefits. Studies have shown that those with higher levels of eumelanin had a lower chance of developing skin cancer than people with lower levels. By absorbing solar heat, and keeping the body cool, eumelanin also helps to regulate body temperature.

The pigment pheomelanin has a lighter yellow-red tint (compound 2 in Figure 1). Because pheomelanin does not absorb UV rays as effectively as eumelanin, those with higher levels have lighter skin tones, and are more prone to skin damage and sunburn. Pheomelanin does, however, have certain benefits. It helps to control body temperature, and can keep the body cool in hot conditions by reflecting heat away from the body. Pheomelanin can also help prevent melanoma and other types of skin cancer.

The gene that controls melanin production for the melanocortin G-protein-coupled receptor 1 (MC1R) is located at gene locus q24.3 on chromosome 16. The MC1R gene regulates tanning (sensitivity to light exposure and sunburn), governs skin and hair color, and raises the risk of melanoma.

The rates of melanin synthesis vary across members of the same family, and between racial groups (Figure 1). This variation (MSH) is caused by genetics, sun exposure, and certain hormones that stimulate melanocytes, such as adrenocorticotropic hormone (ACTH), lipotropin, and melanocyte-stimulating hormone. Using more melatonin results in a grayish-brown skin tone.

2. Causes of Skin Pigmentation

Skin pigmentation is a common condition that can be triggered by various factors. The three leading causes of skin pigmentation are genetics, sun exposure, and particular medications. Understanding the fundamental causes of skin pigmentation will help us understand how to treat and prevent it.

2.1. Genetics

Unexpectedly, 125 genes can influence skin tone. The production of melanin, as depicted in Figure 1, is governed by genes and hormones. A person has control over his or her skin’s ability to function and live, as well as how much pheomelanin or eumelanin they produce by, for instance, deciding how much sun exposure they receive, or the amount of drugs and cosmetics they use. These elements could alter the tone of skin over time. Thus, one of the most frequent reasons for skin color is genetics. Genetics may be able to predict how many melanocytes each individual will have. It is melanocytes, which are skin cells, that make melanin. However, during hyperpigmentation and tanning, melanosomes (the organelles that contain melanin) must be transported and expanded, but during hypopigmentation, melanosomes decrease. Melanin, the pigment that gives skin its color, is more likely to be present in larger concentrations in people with darker skin tones. For example, individuals with darker skin tones frequently have higher melanin levels than those with lighter skin tones.

2.2. Sun Exposure

Sun exposure is a common cause of skin pigmentation. The body produces more melanin, in order to defend itself against UV rays from the sun. This may make the skin more pigmented, to shield it from the sun’s rays. Figure 2 demonstrates how persistent UV exposure leads to the emergence of pigmentation. The following phases make up the formation mechanism. (1) UV radiation produces free radicals. (2) The free radicals and UV light activate biological agents that impact melanocytes, the cells responsible for creating pigment. (3) The enzyme tyrosinase transforms the amino acid tyrosine into melanin pigments, which can be either red or brown in color. (4) Biological substances act to increase the activity of the enzyme Tyrosinase, which generates pigment. (5) Melanin is lost from the skin, as skin cells travel to the surface layers and are shed during the skin’s natural exfoliation process. Melanin is delivered as granules from nearby keratinocytes, to give the skin its color.

2.3. Medications

Several medications may also lighten the skin’s pigment. One class of drugs, antibiotics, can boost melanin synthesis, increasing skin color. When certain medications, such as birth control pills, are taken together, skin pigmentation may also intensify. A person taking medicine should speak with their doctor to find out if the medication could impact the color of their skin.

3. Types of Pigmentation Disorders

While they are ill, a person’s skin tone may alter, becoming lighter (hypopigmentation), as seen in Figure 3A,B, or darker (hyperpigmentation), as seen in Figure 3C,D. Melanin, the pigment that regulates skin color, is produced less frequently by the body, which results in hypopigmentation. Hyperpigmentation, on the other hand, is an increase in melanin synthesis.

3.1. Causes of Hypopigmentation

Prior skin trauma, including skin sores such as blisters, infections, burns, exposure to chemicals, and other wounds, is the most common cause of low melanin content (hypopigmentation). After an injury has healed, the skin will be paler than the surrounding skin surface. Other genetic diseases can result in hypopigmentation in different parts of the skin. As seen in Figure 3, hereditary disorders such as albinism, melasma, fungal infections, pityriasis versicolor, pityriasis alba, and vitiligo can result in hypopigmentation, as seen in the mechanism in Figure 4. At birth, albinism is caused by a genetic abnormality known as low melanin concentration. The prevalent physical traits of albinos include a white complexion, dark blue eyes, and white hair. The genetic melasma condition can cause brown or blue-gray spots to develop on a person’s arms or face. Hormones, sun exposure, or contraceptive medication may bring it on.

Despite the fact that the Malassezia genus is responsible for the widespread fungal infection known as tinea versicolor, also known as pityriasis versicolor, it is possible for fungi to infect humans, and change the color of their skin. Small regions of discoloration are brought on by Malassezia’s alteration of the skin’s normal melanin pigmentation. The patches on the shoulders and buttocks may be lighter or darker than the overall healthy skin tone. Pityriasis alba is a skin condition that typically affects adolescents and teenagers, and is characterized by oval or circular hypopigmented lesions with soft scales. Lesions on the face, upper body, and arms, which are more noticeable in those with darker skin tones, may be modestly erythematous, before becoming hypopigmented.

Depigmentation, which happens when the skin entirely loses pigment and turns white, is another prevalent hypopigmented skin disease. An example of this is the auto-immune condition vitiligo, which is characterized by macules of a white chalky substance on the skin, and melanocyte loss, a common cause of depigmentation. Vitiligo causes smooth, white patches to appear on the skin, as illustrated in examples A and B in Figure 5. Many times, vitiligo is dismissed as a minor problem.

3.2. Causes of Hyperpigmentation

A rise in melanin production causes hyperpigmentation. Examples C and D in Figure 3, and other situations where melanin synthesis increases, primarily result from sun exposure, dermatological conditions, hormones, age, hereditary factors, skin injuries or inflammation, and acne. The most frequent cause of hyperpigmentation is exposure to the sun, which heavily stimulates melanin production. A recent study (Figure 2) demonstrated how early sun exposure might worsen dark spots, by making them resemble melasma, post-inflammatory spots, and age spots. Two examples of hyperpigmentation brought on by hormonal factors are chloasma and melasma. It has been established that the female sex hormones estrogen and progesterone, which boost melanin formation when the body is exposed to sunshine, are to blame for this disease, which is prevalent in women. Hormone replacement therapy has the adverse effect of hyperpigmentation.

Melanocyte counts decline with age, but those that are still present grow and specialize. These physiological alterations show how aging becomes increasingly obvious in people over 40. Genetics has an impact on pigmentation. The development of the melanocyte function, which impacts skin color, requires particular genes. According to the term “post-inflammatory hyperpigmentation”, this appears following several types of skin inflammation or injury, including chemical exposure, burns, wounds, psoriasis or atopic dermatitis, and acne. The skin looks more discolored and blacker after the lesion has healed. The innermost layer of the skin, the dermis, can get infected by papules, pustules, and acne. Unusually dark spots form when skin diseases induce an abnormally high melanin synthesis. Similarly to this, the real causes of the hyper-pigmentation problem are infections of the fatty glands and hair follicles. Mild acne typically doesn’t cause hyperpigmentation. Acne lesions that have been squeezed, squashed, or penetrated will also darken and become more pigmented. Some causes of hyperpigmentation include pregnancy-related birthmarks, age spots, acne scars, and a number of drugs, including antibiotics, birth control pills, antimalarials, and tricyclic antidepressants. A rare condition called Addison’s disease results in black skin patches and decreased adrenal gland activity. Hyperpigmentation can occasionally occur after laser or light treatment.

4. Drugs for Treatment of Skin Pigmentation

Despite being well-recognized for many years, drugs for skin pigmentation have only recently become more widely available. Topical creams and oral pills are the primary medications for skin pigmentation. It would be best to balance the advantages and disadvantages of both medicines to choose which is most beneficial.

4.1. Oral Medications

Oral medicines are a potential substitute for treating skin ailments, and modifying skin tone. Such drugs are beneficial because they are more potent than topical creams, and do not need to be applied or disposed of as frequently as topical creams. However, there are certain drawbacks to taking oral medications. They can be expensive and cause more significant side effects than topical therapies.

Compound 3 in Figure 6 is tranexamic acid (Traxamac® 250 mg), one of several coagulation modifiers. In addition to its use on eczema, melasma, other associated ailments, toxic reactions, and urticaria, and its effects on erythema, itching, swelling, and other recognized symptoms, it has also been used to treat various illnesses. A plasmin inhibitor, tranexamic acid prevents the plasminogen activator from converting plasminogen to plasmin, by reversibly shutting off lysine binding sites on plasminogen molecules. This reduces atypical fibrinolysis, and prevents blood loss. According to recent studies, tranexamic acid helps tyrosinase to untangle tangles. It might avoid and stop hyperpigmentation, by reducing melanin production. It is a widely used pharmaceutical technique that is easily accessible and effective against pigment spots. Although it inhibits the effects of tyrosinase, and changes the relationship between keratinocytes and melanocytes, it decreases dermal vascularity, and lessens melanin production.

Using tranexamic acid orally, in a dosage of 250 mg twice daily for six months, on 75 patients, a clinical and photographic evaluation revealed an initial decline in melasma after the first month for 82.4% of patients, and 94.6% in the second month. The development of pigmentation had been used to measure the treatment’s success (excellent if >90%, good if >60%, fair if >30%, and poor if 30%). After six months, the overall development rate was 95.9%, with 10.8% being excellent, 54% being good, and 31.1% being fair, which is evidence that oral tranexamic acid is a safe and effective melasma treatment.

Mexameter® was utilized to evaluate the suggested lesional melanin index (MI) ranks, and the erythema index (EI) scores, for 25 patients who received 1500 mg twice daily for two months. Both of these scores fell off dramatically. Histological examination confirmed significant decreases in mast cell counts, vessels, and epidermal pigmentation. Here is an illustration of how oral tranexamic acid reversed melasma-related dermal changes, including increased vascularity, decreased mast cell populations, and decreased melasma-related epidermal pigmentation.

In this study of 25 women, certain sides of the face received twice-daily applications of 5% topical tranexamic acid for 12 weeks, as a melasma treatment. The Mexameter and Melasma Area and Severity Index (MASI) results revealed a notable drop in the MI and MASI scores. Additionally, for 12 weeks, 23 melasma patients applied a 2% tranexamic acid emulsion twice daily to their whole faces. With a rise in the lightness values, and a decrease in the erythema values, the mMASI and chromameter results showed a significant improvement in the fourth and eighth weeks.

Isotretinoin is the 13-cis-retinoic acid derivative of vitamin A (Isotane® 20 mg, molecule 4 in Figure 6). In treating acne vulgaris, oral isotretinoin exerts its effects by reducing sebaceous gland activity, the development of Propionibacterium acnes, and inflammation. This facilitates pore cleaning, and inhibits the growth of new lesions.

The administration of 20 mg of Accutane (isotretinoin) orally was randomly assigned to 60 patients (aged 35 to 65); 42 of the women, and 18 of the men. It was administered three times a week for no more than two months, and tracking continued for months after the study was over. The 60 patients reported reductions in their wrinkles, pore thickness, and pore size. They noticed that the skin became significantly smoother and lighter in color. Both the elasticity and the tone of the skin improved. Additionally, they noticed a decrease in pigmented lesions and hyperpigmentation.

The severity of acne was assessed using the MASI for 30 individuals of either sex who were receiving 20 mg of isotretinoin as a monotherapy, and were between the ages of 18 and 25. A reduction of roughly 73.4% was seen in patients who took 20 mg of oral isotretinoin for 16 weeks.

4.2. Topical Creams

Topical creams are the most common type of drug used to treat skin pigmentation. They are applied directly to the affected area, and can lighten or darken the skin. The main advantage of topical creams is that they can be used at home, and do not require a trip to the doctor. Additionally, they are typically less expensive than oral medications. Topical cream application, however, comes with several drawbacks. They can be messy and time-consuming to apply, and they may only sometimes be as effective as oral medications.

Topical steroids are the most often recommended drug in dermatology. They are prescribed for various conditions, including eczema, psoriasis, atopic dermatitis, lichen simplex chronicus, intertrigo, and psoriasis, due to their immunosuppressive, anti-mitogenic, and anti-inflammatory characteristics. The dosage varies from one to three times per day. Betamethasone 0.05% (Betnovate-N®, chemical 5 in Figure 7) and clobetasol 0.05% (Dermovate®, compound 6 in Figure 7) are examples of topical steroids. The NF-Kappa B inhibitors betamethasone and clobetasol are glucocorticoids that prevent neutrophil apoptosis and demarginating. Betamethasone and clobetasol are phospholipase A2 inhibitors, which also reduce the production of arachidonic acid derivatives. Additionally, glucocorticoids encourage the anti-inflammatory gene interleukin-10, a common ingredient in cream or ointment treatments. Numerous local and systemic adverse effects of topical steroids have been attributed to their continuous use.

A total of 15 vitiligo patients of both sexes (F:M 1.14:1) utilized betamethasone cream 0.05% twice daily throughout a three-month study. Based on a patient’s degree of minimal pigmentation/no reaction, moderate, noticeable pigmentation, or outstanding pigmentation, the improvement of each patient was rated as (25%), (25–50%), (50–75%), or (>75%), respectively. Compared to 40.0% of patients with limited pigmentation or no reaction, 46.7% and 13.3% showed a moderate or outstanding pigmentation response after therapy.

A total of 731 patients with moderate to severe plaque psoriasis, with 3% to 20% body surface area, participated in the 4-week Clobetasol Spray trial, which used two doses of clobetasol propionate spray 0.05% twice daily as treatment. The change in target plaque severity was the primary outcome measure. According to the major outcome measures scale, 80.0% of the patients in the therapy group were clear or nearly unambiguous, and showed a decrease in severity from the beginning.

A topical anti-infective cream, silver sulfadiazine (Silvadene®, chemical 7 in Figure 7) is primarily used to prevent and cure burn injuries. Silver sulfadiazine solution with 1% API dissolves in water. Proteins become denaturized and enzyme activity is reduced by silver ions. Additionally, silver ions bind to proteins and surface membranes, leading to membrane proton leakage and cell death. Sulfadiazine competitively inhibits PABA, a naturally occurring bacterial substance that acts as a substrate for the dihydropteroate synthase enzyme. These organisms must carry out the blocked process to produce folic acid. Silver sulfadiazine exhibits broad-spectrum action against both gram-positive and gram-negative pathogens. It has been demonstrated that it promotes wound and injury repair, and has anti-infective qualities. Twenty-seven individuals with 2° burn injuries were randomly assigned to receive silver sulfadiazine throughout a 4-week study. After four weeks of treatment, the healing condition of 2° deep dermal burn wounds were determined to be (0–25%), (26–50%), (51–75%), or (76–100%), respectively, as poor healing, moderate healing, fast healing, or excellent healing. While eight and thirteen patients showed a mild and quick recovery, respectively, six patients with 2° deep dermal burn lesions showed poor healing. Mixtures of creams, shampoos, powders, mouthwash, and gels contain both an anti-infective and a steroid component, to treat skin or scalp infections. Triamcinolone and dimethicone are ingredients in the drug TriHeal80® (see components 8 and 9 in Figure 7). Topical corticosteroids produce similar antipruritic, anti-inflammatory, and vasoconstrictive effects.

Triamcinolone is a phospholipase A2 inhibitor that acts on cell membranes, to prevent the lysosomal membranes of leukocytes from rupturing. This prevents the production of arachidonic acid, which in turn lowers lipoxygenase and cyclooxygenase, while inhibiting the production of prostaglandins and leukotrienes. Dimethicone, a silicone oil, exhibits viscoelastic qualities. It has moisturizing properties, and is utilized as a surfactant, antifoaming agent, and lubricant to cure skin irritation. To reduce the rate of water evaporation, dimethicone is used topically. When used four times per day for two months, and monitored for another two months, triamcinolone 0.1% mouthwash successfully treated oral lichen planus in 20 patients. All effectiveness endpoints, assessed using the visual analog scale, the verbal health impact profile score, and the objective clinical score, revealed a significant improvement in the patients.

Under the brand name Tri-Luma®, a triple combination cream is sold that includes the active components tretinoin, hydroquinone, and fluocinolone in concentrations of 0.01%, 4%, and 0.05%. Hydroquinone is the most frquently used skin-lightening or depigmenting substance (compound 10 in Figure 7). It treats dyschromic skin diseases such as melasma, chloasma, freckles, and post-inflammatory hyperpigmentation, by suppressing melanin production. It stops tyrosinase from converting L-3,4-dihydroxyphenylalanine into melanin, due to its structural similarity to a specific analog of melanin. Fluocinolone (molecule 11 in Figure 8) treats symptoms, including itchiness, swelling, and redness caused by skin problems. Retinol (compound 12 in Figure 8) cures skin aging. It has been shown that it might be beneficial for concerns related to skin aging. The most remarkable feature is that treatment results manifest eight to twelve months after using the tretinoin 0.1% cream preparation. The most frequent side effects of tretinoin include very slight skin irritability, and a transient, mild, and clinically uncomfortable burning sensation. Sixty patients with moderate (grade 2) or severe (grade 3) melasma received treatment for eight weeks with the triple combination cream. At weeks 4, 6, and 8, the triple combination cream significantly improved the overall results, with an improvement rate of 73% (44/60). The percentage of participants who thought the triple combination cream was “excellent” as a treatment was 50%, while the most frequently mentioned adverse effects were erythema, burning, and desquamation.

Additionally, a 12-week open-label trial was created, to gauge the effectiveness and safety of applying topical retinol 0.15% twice daily. At the fourth, eighth, and twelve weeks, it was found that 39%, 77%, and 77% of patients, respectively, showed significant improvement. When using topical retinol, dryness, erythema, peeling, stinging, and burning were some side effects that were reported.

Dermatitis, eczema, rashes, and allergies are just a few of the skin conditions that TriDerm® is used to treat. The swelling, redness, and itching that are brought on by these various disorders are reduced by triamcinolone. It includes corticosteroids that range in strength from mild to potent. The mechanism of action of TriDerm is composed of betamethasone, clotrimazole, and gentamicin (compounds 13 and 14 in Figure 8). This results in the antipruritic, anti-inflammatory, and vasoconstrictive effects of betamethasone, as well as the broad-spectrum bactericidal antibiotic effect of gentamicin, and the broad-spectrum antifungal effect of clotrimazole. The contents of the cell leak out when clotrimazole reacts with the fungal cell membrane. Gentamicin is an effective topical skin therapy for bacterial infections. A study included 68 patients with itchy dermatoses, including atopic dermatitis, contact dermatitis, and true eczema. Of the patients, 33 received a twice-daily application of a topical cream containing betamethasone, clotrimazole, and gentamicin on the affected body parts. The effectiveness of the therapy was assessed after 7, 14, and 28 days. On the seventh day of treatment, there was a reduction in the inflammatory process and subjective symptoms. Of the 33 patients, 5 saw a scientific recovery on the fourteenth day of receiving treatment. After 28 days of therapy, the patients had fully recovered medically.

The main component of the topical anti-cancer drug Opzelura® is ruxolitinib (compound 15 in Figure 8). A class of drugs known as Janus kinase inhibitors, which includes roxolitinib, has an effect on the immune system. JAK inhibitors may reduce the immune system’s ability to fight off infections. JAKs serve a variety of purposes. JAK1 and JAK3 increase lymphocyte existence and differentiation, whilst JAK2 increases the signal transduction of thrombopoietin and erythropoietin. JAKs are located in the cytoplasmic region of cytokine and growth factor receptors. JAKs are also activated, and undergo cross- and tyrosine phosphorylation. Ruxolitinib has a low affinity for JAK3, but is a solid and selective inhibitor of JAK2 and JAK1. Ruxolitinib reduces the plasma levels of pro-inflammatory cytokines, and inhibits myeloproliferative neoplasms by downregulating the JAK-STAT pathway.

Randomized controlled trials recommended using ruxolitinib 1.5% cream for treating vitiligo twice daily in various patients. This was shown to demonstrate clinically excellent re-pigmentation of all body areas, including the acral region, after 24 weeks, with continued improvement through week 52. It was tolerated well in patients with long-standing high contamination.

Salicylic acid (Salvax®, compound 16 in Figure 8), podophyllum resin (Podocon-25®, compound 17 in Figure 9), and podofilox (Condylox®, compound 18 in Figure 9) are a few examples of topical keratolytics that are administered topically to the skin, to soften keratin. This facilitates the peeling of skin cells, supports the skin’s capacity to retain moisture, and aids in the treatment of dry skin conditions, and is generally used to treat skin diseases, such as psoriasis, warts, keratoses, and acne. More topical brand names used for reducing skin pigmentation are included in Table 1.

Because of its keratolytic qualities, salicylic acid, a lipophilic B-hydroxy acid, is frequently used in cosmetic product formulations as a skin scaler for lightening. Arachidonic acid is reduced from converted prostaglandins and thromboxanes by COX-1 and COX-2 inhibitors. Salicylic acid also has anti-inflammatory and antibacterial effects. Twenty Latin American women over the age of 18 with moderate to severe bilateral melasma participated in a small, potential randomized controlled trial to compare the efficacy of salicylic acid 20–30% scaler every two weeks, followed by up to eight weeks, in combination with hydroquinone 4% twice daily for 14 weeks, versus hydroquinone 4% alone. A narrowband reflectance spectrophotometer (Mexameter MX-16) was used to quantify the degree of pigmentation on the affected and unaffected skin on each face. The Melasma Area and Severity Index (MASI) was used to assess the severity of the melasma. Of the patients, 33% were regarded as showing a mild development and slight improvement, with 44% showing more significant progress on the peeled side. One patient (6%) was noted to show only slightly more growth on the unpeeled side. The peeled side had advanced more than the unpeeled side, according to 83% of the nonblinded patients (four somewhat, seven moderately, and four significantly). One patient (6%) thought the unpeeled side was more advanced, whereas twelve percent (12%) believed there was no difference. Table 2 shows a summary of the drugs and natural hyperpigmentation meta-analysis studies.

5. Natural Hyperpigmentation Treatment

Despite the wide range of therapies available, a growing number of people are choosing plants and natural items as alternatives. Plant-based and natural remedies have long been used to treat skin issues, and they are gaining popularity as a secure and efficient method to treat skin hyperpigmentation.

Vitamins A, B, C, and E can all be used to address skin pigmentation problems, and are necessary for healthy skin. Each vitamin, which can be obtained from foods or supplements, has specific advantages.

Niacin, pantothenic acid, and biotin are the B vitamins most frequently found in skincare products. Niacin, also known as niacinamide, is a vitamin that is used in face creams and masks, to minimize the appearance of enlarged pores, fine lines, and dullness. Pantothenic acid is also applied to dry, flaky skin, as a moisturizer. Numerous hair, nail, and skincare products include biotin. Ascorbic acid (vitamin C), an antioxidant, inhibits tyrosinase by binding to copper, and suppressing the oxidative polymerization of melanin precursors, which prevents melanin synthesis in the melanogenesis pathway. A statistically significant decrease from the baseline to week 16 was observed in a trial on 39 patients, using 25% L-ascorbic acid dissolved in Nmethyl-2-pyrrolidone and dimethyl isosorbide, as indicated by MASI values and mexameter data. A particular type of vitamin E is alpha-tocopheryl acetate. When fat is subjected to oxidation, and during the spread of free radical reactions, vitamin E, a powerful chain-breaking antioxidant, prevents the synthesis of reactive oxygen species molecules.

Artocarpus lakoocha and Glycyrrhiza glabra extracts have been reported to exhibit tyrosinase inhibitory effects and melanin pigment reduction. For the treatment of hyperpigmentation, the combination of 9:1 Artocarpus lakoocha and Glycyrrhiza glabra decreased melanin pigment by up to 53% in B16 cells, by lowering the production of tyrosinase (TYR), microphthalmia-associated transcription factor (MITF), and tyrosinase-related protein-2 (TRP-2).

Antioxidants and fatty acids included in oils such as rosehip, jojoba, and argan oil aid in reducing inflammation, and brightening the skin. Natural oils can also shield the skin from the effects of the environment, preventing further discoloration. Aloe vera also includes aloin (compound 19 in Figure 9), which has been demonstrated to lighten skin, and function well as a nontoxic hyperpigmentation therapy. Sharique described aloe vera as a natural depigmenting ingredient.

When used as an emollient, jojoba oil exhibits first-rate lubricity, without having an oily or greasy texture, in single-segment and emulsion structures. It can also contribute to the skin’s effective water regulation during transpiration, reducing evaporation without obstructing the passage of gases or water vapor. According to a study, jojoba oil (or its ozonized or hydrogenated derivatives) has emollient properties. The study discovered that a significant increase in skin surface flexibility developed within 5 min and persisted for hours, suggesting a potential application in solutions for dry skin. Jojoba liquid wax was found to be just as effective at treating diaper rash as triamcinolone acetonide, nystatin, neomycin, and gramicidin. Jojoba oil is also an anti-inflammatory. Due to the absence of systemic adverse effects, jojoba has the benefit of being safer. Additionally, it has anti-acne and anti-psoriasis qualities, which allow the dissolution of sebum deposits through the hair follicles, due to its capacity to infiltrate the follicles, eliminate the comedones, and clear the skin.

In a research study, ten women used argan oil as a bandage on their skin for 28 days. None of the women experienced itching, or noticed any skin irritation or redness, demonstrating the oil’s efficacy in reducing the amount of pigmentation. These women did observe a minor decrease in melanin content in the vicinity of the bandage, though, which lends credence to the idea that the oil lessens pigmentation. Licorice root extract, turmeric extract, and green tea extract are other herbal extracts high in antioxidants that help to reduce inflammation and brighten the skin.

Since ancient times, licorice root extract has been utilized for its medical benefits, particularly for skin care. It contains glycyrrhizin, which has been shown to have antioxidant and anti-inflammatory properties. Given that it is thought to help enhance skin appearance and treat some skin disorders, these qualities make it a popular ingredient in skincare products. Several research studies have been conducted to determine whether licorice root extract is effective for treating skin conditions. According to a study, licorice root extract is useful for reducing hyperpigmentation and lightening the skin. Atopic dermatitis symptoms may be lessened by licorice root extract, according to a different study. James M. Spencer also demonstrated in his research that licorice root extract was efficient in lessening the severity of rosacea, melasma, and acne. Additionally, licorice root extract reduced the appearance of black spots and redness, as was discovered in a 2019 study by Maria Yusuf Dhariwala.

Since ancient times, turmeric extract has been valued for its therapeutic benefits. It has a yellow tint, and various health advantages, due to the presence of the active component curcumin, when it comes to pigmentation and skin conditions. The strong anti-inflammatory qualities found in curcumin can help lessen the skin inflammation brought on by a variety of skin conditions, including psoriasis and eczema. Antioxidants included in turmeric extract reduce oxidative damage that can cause skin aging, and pigmentation disorders such as melasma, by neutralizing free radicals. Curcumin also has skin-lightening qualities. By preventing the formation of the melanin-producing enzyme tyrosinase, it can lessen hyperpigmentation, and make the skin lighter. Curcuminoids, which are found in turmeric, have exfoliating qualities that aid in gently removing dead skin cells, and encourage skin regeneration, minimizing the appearance of hyperpigmentation and dark patches. The use of turmeric extract to treat skin issues was the subject of a 2018 study by Alexandra R. Vaughn. In psoriasis, eczema, and acne patients, the study found that turmeric extract was beneficial in lowering skin inflammation, and enhancing skin health. According to a 2018 study by Penelope J. Kallis, a topical cream with turmeric extract proved successful in lowering the severity of acne in patients after four weeks of treatment.

Another organic component that has been investigated for its therapeutic advantages for the skin is green tea extract. It has many polyphenols and antioxidants, as well as anti-inflammatory and skin-protective qualities. Green tea extract works in a variety of ways, to treat pigmentation issues and skin problems. Catechins and epigallocatechin gallate (EGCG), two antioxidants found in green tea, work to combat free radicals that can damage skin and speed up the aging process. Green tea extract also has strong anti-inflammatory qualities that can help lessen the skin irritation brought on by a variety of skin diseases, such acne, eczema, and rosacea. The EGCG in green tea extract can help inhibit tyrosinase activity, reducing the production of melanin, and thus lightening the skin. Furthermore, green tea extract has been shown to offer some protection against UV radiation, which can cause skin damage and contribute to pigmentation disorders. A clinical study was conducted on 11 patients to investigate the use of green tea extract in treating acne; this study found that green tea extract was effective in reducing the number of acne lesions and improving overall skin health. Another study, published in 2018, found that green tea extract effectively reduced the appearance of fine lines and wrinkles in the skin.

Kojic acid (Enshine® cream 2%, compound 20 in Figure 9) has been found to be effective in treating various skin disorders and pigmentation issues, due to its mechanism of action. It works by inhibiting the activity of tyrosinase, which reduces the production of melanin, which can help to fade dark spots and hyperpigmentation. In addition to its tyrosinase-inhibiting properties, kojic acid has antioxidant and anti-inflammatory properties; these can be particularly beneficial to individuals with acne, rosacea, and other inflammatory skin conditions. One study, published in 2016 by Peter J. Gust, evaluated the efficacy of a cream containing 2% kojic acid, 10% glycolic acid, and 2% hydroquinone for treating melasma. The study involved 40 participants, who applied the cream twice daily for 12 weeks. The results showed a significant reduction in the severity of melasma in the treated group, compared to the control group, with no reported adverse effects. In another study, Tamara Searle investigated the use of a cream containing 2% kojic acid, 1% arbutin, and 5% vitamin C to treat age spots. The study involved 60 participants, who applied the cream twice daily for 12 weeks. The results showed a significant reduction in the number and severity of age spots in the treated group, compared to the control group, with no reported adverse effects. Several herbs and naturally occurring substances that are commonly used in skincare products, for their ability to lighten skin and reduce hyperpigmentation, are listed in Table 3.

Phlorotannins (compound 21 in Figure 9) from brown algae (brown seaweed) play a crucial role in the reduction of hyperpigmented effects, and the prevention of premature skin aging. They protect the skin from the sun’s infrared and blue rays.

Additionally, they promote cellular energy generation, which raises the oxygenation of the skin. Through this technique, the skin’s overall appearance and cell innovation are improved. Their antioxidant action prevents the collagen that firms the skin from degenerating. Phlorotannins have been studied for their impact on skin conditions and pigmentation, in clinical trials and meta-analyses. A randomized, double-blind, placebo-controlled study in 2022 discovered that women with dry skin saw improvements in skin hydration, suppleness, and wrinkle formation with an Ecklonia cava (Phaeophyceae) extract high in phlorotannins. Another randomized, double-blind, placebo-controlled study discovered that a phlorotannin-rich Ascophyllum nodosum extract reduced face pigmentation, and enhanced skin suppleness, in women with age spots.

Researchers have looked into the potential for marine-derived compounds from Undaria pinnatifida, Octopus vulgaris, and Sargassum polycystum, to improve skin pigmentation, as well as to possess antioxidant, anti-inflammatory, and immunomodulatory capabilities. These substances (compounds 22–24 in Figure 9) also contain octaphlorethol A, fucoidan, and fucoxanthin. Numerous studies have looked into how octaphlor-ethol A affects skin conditions and pigmentation. According to one study, in human melanoma cells, octaphlorethol A inhibited the formation of melanin, and decreased skin pigmentation. In a different study, mice with atopic dermatitis showed enhanced skin barrier function and reduced inflammation when treated with octaphlorethol A. Additionally, a cream containing fucoidan and marine collagen enhanced skin hydration, suppleness, and wrinkle formation in women with dry skin, according to a randomized, double-blind, placebo-controlled research study. Additionally, a cream containing fucoidan and marine collagen enhanced skin hydration, suppleness, and wrinkle formation in women with dry skin, according to a randomized, double-blind, placebo-controlled research study. Fucoxanthin, a carotenoid pigment, was found to be associated with a significant decrease in the severity of melasma in a review of 11 randomized controlled studies. To corroborate these findings, more research is required, as the authors stated that the quality of the inclusive studies was generally low.

6. Modern Skin Pigmentation Treatments and Promising New Technologies

The preferred method of treatment for problems with skin pigmentation has long been laser therapy. The melanin in the skin can be reduced and evened out by lasering the afflicted area, leading to a more even complexion. As time goes on, technological developments mean that lasers are more and more efficient. Today, pigmentation can be targeted in deeper, more covert locations, thanks to laser technology. For instance, lasers can now be used to target pigment under the skin’s surface, without causing irritation or damage to the skin! As a result, problems such as age spots and sun damage can be treated without any negative consequences or discomfort. To remove obstinate pigmentation, the most recent lasers combine optical energy with intense pulsed light (IPL). This is an exciting development, as it makes it possible to treat patients more quickly and effectively than ever before.

Topical creams and serums are among the newest and most promising therapies for skin pigmentation. These remedies include substances such as niacinamide, kojic acid, licorice extract, and mulberry extract that are especially made to fight pigmentation. These cutting-edge chemicals have the potential to significantly reduce dark spots, lighten skin tone, and enhance the skin’s overall clarity and texture. For instance, kojic acid can limit tyrosinase activity, which helps to prevent hyperpigmentation from occurring, and niacinamide can suppress melanin formation, which helps to reduce skin discoloration. In order to prevent the skin from experiencing any unpleasant reactions or side effects, the treatment should also be free of parabens and other harmful preservatives. In order to diminish pigmentation, micro-needling is a process used to increase the skin’s natural collagen and elastin production. In order to provide a more exact therapy, the technique now involves using specialized instruments. Small needles are used in the procedure, to puncture the skin and create microscopic channels that can only be seen under a microscope. This straightforward procedure enhances collagen synthesis, while promoting the skin’s natural ability to mend itself. Overall, with excellent outcomes, micro-needling is quickly rising to the top of the list of popular methods for lightening skin. Typically, chemical peels are used to remove the top layers of skin, which lessens the visibility of dark patches. Combination treatments, however, are far more effective for the skin. Combination therapies are proving to be even more effective at minimizing dark spots. These combination treatments include several acids, such as glycolic acid and lactic acid, which, when used together, can be much more potent than when used separately. These combined therapies, which neither lasers nor light-based devices can currently offer, can help with both facial discoloration, and uneven pigmentation on other parts of the body, with only one treatment.

With the development of new technology, the future of skin pigmentation therapies appears to be more promising than ever. One of the most promising new therapies for diseases of skin pigmentation is plasma pen therapy. Freckles, age spots, sunspots, and melasma can all be treated using this technique, which removes pigment from the skin by means of a targeted plasma energy beam. Compared to previous therapies, this one is less intrusive, and has fewer adverse effects.

The use of radiofrequency therapies to treat diseases of skin pigmentation is growing in popularity. The appearance of dark areas, and the overall tone and texture of the skin, can be improved by this technology, which uses radio waves to break down melanin deposits in the skin. Radiofrequency treatments are quick, non-invasive, safe, and do not entail a long recovery time.

7. Conclusions

Skin pigmentation is the phrase used to describe the color of someone’s skin, which is determined by how much melanin is produced by melanocytes in their skin. The two main types of melanin are eumelanin and pheomelanin. Eumelanin, which defends against skin cancer and sun damage, is the cause of dark skin tones. Pheomelanin, on the other hand, causes lighter skin tones, has the ability to regulate body temperature, and provides protection against skin cancer. The causes of skin pigmentation include genes, sun exposure, hormonal changes, skin traumas, and some medications. Other anomalies of skin pigmentation, such as vitiligo, albinism, and melasma, are brought on by genetic changes. Hyperpigmentation and hypopigmentation are the two basic types of skin pigmentation. When melanin is produced excessively, it causes hyperpigmentation, which manifests as darker spots of skin. This can be influenced by the sun, hormonal changes, and particular medications. Hypopigmentation, which results in lighter regions of skin, is brought on by melanin loss. This can be caused by genetic conditions, skin traumas, and certain medicines. In recent years, we have seen an increase in the use of oral tablets and topical lotions to treat skin pigmentation. In addition to being more costly, oral drugs have more serious adverse effects than topical treatments. Clinical studies and meta-analyses have demonstrated that oral medication in the form of tablets containing tranexamic acid and isotretinoin can be used to treat a variety of skin disorders, such as eczema, melasma, and other associated conditions. Because they are often less expensive than oral drugs, and can be used at home, topical creams are the most popular type of medication used to treat skin pigmentation. The most frequently prescribed treatments for skin diseases are topical steroids, which have a number of disadvantages compared to oral prescriptions, including messiness, and an occasionally lesser efficacy. Additionally, caution must be exercised, to prevent the negative consequences of the continuous usage of topical steroids. Additionally, clinical studies have shown that the topical versions of salicylic acid, tretinoin, betamethasone, clobetasol, triamcinolone, dimethicone, fluocinolone, hydroquinone, and silver sulfadiazine are useful in treating skin conditions. Along with octaphlorethol A, fucoidan, and fucoxanthin marine extracts, natural extracts such as rosehip, jojoba, argan oil, aloe vera, licorice root, curcumin, green tea, and kojic acid have potent anti-inflammatory properties that can help reduce inflammation in the skin caused by a variety of skin conditions, such as acne, eczema, and rosacea. With the development of technology, laser therapy has long been the preferred method of treating skin pigmentation problems. Lasers are now more efficient, thanks to ongoing technical developments that provide higher precision, faster healing times, and better outcomes. While micro-needling is a process intended to promote the skin’s natural synthesis of collagen and elastin, to diminish pigmentation, topical creams and serums contain cutting-edge chemicals created to combat pigmentation.

Combination treatments, which use a combination of acids to lessen the appearance of dark spots, are becoming more and more popular for treating skin pigmentation disorders. Promising technologies such as plasma pen therapy and radiofrequency treatments are also gaining popularity.

References 219

  1. 1.
    Clinical and Biological Characterization of Skin Pigmentation Diversity and Its Consequences on UV Impact · 2018
    No notice
  2. 2.

    Martin A.R., Lin M., Granka J.M., Myrick J.W., Liu X., Sockell A., Atkinson E.G., Werely C.J., Möller M., Sandhu M.S., et al. An unexpectedly complex architecture for skin pigmentation in Africans. Cell. 2017;171:1340-1353.

    Not in our library10.1016/j.cell.2017.11.015

  3. 3.

    Nasti T.H., Timares L. MC 1R, Eumelanin and Pheomelanin: Their role in determining the susceptibility to skin cancer. Photochem. Photobiol. 2015;91:188-200.

    Not in our library10.1111/php.12335

  4. 4.
    Photoprotection and Skin Pigmentation: Melanin-Related Molecules and Some Other New Agents Obtained from Natural Sources · 2020
    No notice
  5. 5.

    Polidori C., Jorge A., Ornosa C. Eumelanin and pheomelanin are predominant pigments in bumblebee (Apidae: Bombus) pubescence. PeerJ. 2017;5:e3300-e3321.

    Not in our library10.7717/peerj.3300

  6. 6.

    Hu S., Zhai P., Chen Y., Zhao B., Yang N., Wang M., Xiao Y., Bao G., Wu X. Morphological characterization and gene expression patterns for melanin pigmentation in Rex rabbit. Biochem. Genet. 2019;57:734-744.

    Not in our library10.1007/s10528-019-09929-x

  7. 7.

    Baek S.H., Lee S.H. Sesamol decreases melanin biosynthesis in melanocyte cells and zebrafish: Possible involvement of MITF via the intracellular cAMP and p38/JNK signalling pathways. Exp. Dermatol. 2015;24:761-766.

    Not in our library10.1111/exd.12765

  8. 8.

    Madelaine R., Ngo K.J., Skariah G., Mourrain P. Genetic deciphering of the antagonistic activities of the melanin-concentrating hormone and melanocortin pathways in skin pigmentation. PLoS Genet. 2020;16:e1009244-65.

    Not in our library10.1371/journal.pgen.1009244

  9. 9.

    Ozdeslik R.N., Olinski L.E., Trieu M.M., Oprian D.D., Oancea E. Human nonvisual opsin 3 regulates pigmentation of epidermal melanocytes through functional interaction with melanocortin 1 receptor. Proc. Natl. Acad. Sci. USA. 2019;116:11508-11517.

    Not in our library10.1073/pnas.1902825116

  10. 10.
    Melanocortin 1 Receptor: Structure, Function, and Regulation · 2016
    No notice
  11. 11.

    Suherlan S., Fakih T.M., Effendi D.H. Uji In-Silico Aktivitas Melanogenesis Senyawa Ternatin Bunga Kembang Telang (Clitoria ternatea) terhadap Reseptor Tirosinase. Pros. Farm. 2021;7:849-856.

    Not in our library

  12. 12.

    Jablonski N.G. The evolution of human skin pigmentation involved the interactions of genetic, environmental, and cultural variables. Pigment Cell Melanoma Res. 2021;34:707-729.

    Not in our library10.1111/pcmr.12976

  13. 13.

    Ainger S.A., Jagirdar K., Lee K.J., Soyer H.P., Sturm R.A. Skin pigmentation genetics for the clinic. Dermatology. 2017;233:1-15.

    Not in our library10.1159/000468538

  14. 14.

    Feng Y., McQuillan M.A., Tishkoff S.A. Evolutionary genetics of skin pigmentation in African populations. Human Mol. Genet. 2021;30:88-97.

    Not in our library10.1093/hmg/ddab007

  15. 15.

    Kita R., Fraser H.B. Local adaptation of sun-exposure-dependent gene expression regulation in human skin. PLoS Genet. 2016;12:e1006382.

    Not in our library10.1371/journal.pgen.1006382

  16. 16.

    Armenta A.M., Henkel E.D., Ahmed A.M. Pigmentation disorders in the elderly. Drugs Aging. 2019;36:235-245.

    Not in our library10.1007/s40266-018-00633-w

  17. 17.

    Adigun C.G. Adverse drug reactions of the lower extremities. Clin. Podiatr. Med. Surg. 2016;33:397-408.

    Not in our library10.1016/j.cpm.2016.02.007

  18. 18.

    Nicolaidou E., Katsambas A.D. Pigmentation disorders: Hyperpigmentation and hypopigmentation. Clin. Dermatol. 2014;32:66-72.

    Not in our library10.1016/j.clindermatol.2013.05.026

  19. 19.

    Böhm M. Disorders of Melanin Pigmentation. Braun-Falco’s Dermatology. 2021;1-35.

    Not in our library

  20. 20.

    Ma E.Z., Zhou A.E., Hoegler K.M., Khachemoune A. Oculocutaneous albinism: Epidemiology, genetics, skin manifestation, and psychosocial issues. Arch. Dermatol. Res. 2023;315:107-116.

    Not in our library10.1007/s00403-022-02335-1

  21. 21.

    Federico J.R., Krishnamurthy K. Albinism. StatPearls. 2022.

    Not in our library

  22. 22.

    Lee D.Y., Kim C.R., Lee J.H. Trichrome vitiligo in segmental type. Photodermatol. Photoimmunol. Photomed. 2011;27:111-112.

    Not in our library10.1111/j.1600-0781.2011.00572.x

  23. 23.

    Hill J.P., Batchelor J.M. An approach to hypopigmentation. BMJ. 2017;356:356-362.

    Not in our library10.1136/bmj.i6534

  24. 24.

    Silpa-Archa N., Kohli I., Chaowattanapanit S., Lim H.W., Hamzavi I. Postinflammatory hyperpigmentation: A comprehensive overview: Epidemiology, pathogenesis, clinical presentation, and noninvasive assessment technique. J. Am. Acad. Dermatol. 2017;77:591-605.

    Not in our library10.1016/j.jaad.2017.01.035

  25. 25.

    Kallini J.R., Riaz F., Khachemoune A. Tinea versicolor in dark-skinned individuals. Int. J. Dermatol. 2014;53:137-141.

    Not in our library10.1111/ijd.12345

  26. 26.

    Miazek N., Michalek I., Pawlowska-Kisiel M., Olszewska M., Rudnicka L. Pityriasis Alba—Common Disease, Enigmatic Entity: Up-to-Date Review of the Literature. Pediatr. Dermatol. 2015;32:786-791.

    Not in our library10.1111/pde.12683

  27. 27.

    Jing J., Man X.Y. Vitiligo-like depigmentation in a patient treated with PD-1 antibody. BMJ. 2021;374:n1982.

    Not in our library10.1136/bmj.n1982

  28. 28.

    McMichael L. Skin camouflage. BMJ. 2012;344:d7921.

    Not in our library10.1136/bmj.d7921

  29. 29.
    Periorbital hyperpigmentation: A study of its prevalence, common causative factors and its association with personal habits and other disorders · 2014
    Not checked
  30. 30.

    Choi W., Yin L., Smuda C., Batzer J., Hearing V.J., Kolbe L. Molecular and histological characterization of age spots. Exp. Dermatol. 2017;26:242-248.

    Not in our library10.1111/exd.13203

  31. 31.

    Baxter L.L., Pavan W.J. The etiology and molecular genetics of human pigmentation disorders. Wiley Interdiscip. Rev. Dev. Biol. 2013;2:379-392.

    Not in our library10.1002/wdev.72

  32. 32.

    Yadalla H.K.K., Aradhya S. Post acne hyperpigmentation: A brief review. Our Dermatol. Online. 2011;2:230-231.

    Not in our library

  33. 33.

    Plensdorf S., Livieratos M., Dada N. Pigmentation disorders: Diagnosis and management. Am. Fam. Physician. 2017;96:797-804.

    Not in our library

  34. 34.

    Woolery-Lloyd H., Kammer J.N. Treatment of Hyperpigmentation. Seminars in Cutaneous Medicine and Surgery. 2011;Volume 30:171-175.

    Not in our library10.1016/j.sder.2011.06.004

  35. 35.

    Bala H.R., Lee S., Wong C., Pandya A.G., Rodrigues M. Oral tranexamic acid for the treatment of melasma: A review. Dermatol. Surg. 2018;44:814-825.

    Not in our library10.1097/dss.0000000000001518

  36. 36.

    Ali A.A., Al-Obaidi Z.M.J., Raauf A.M., Mahmood H.S. A Comparative, Randomized, Double-Blinded, and Vehicle-Controlled Study for the Reduction in Facial Pigmentation after Treatment with both Tranexamic Acid and Tranexamic Acid Ethyl Ester. Syst. Rev. Pharm. 2020;11:563-567.

    Not in our library

  37. 37.

    Kaur A., Bhalla M., Sarkar R. Tranexamic acid in melasma: A review. Pigment Int. 2020;7:12-25.

    Not in our library

  38. 38.

    Maeda K. Mechanism of Action of Topical Tranexamic Acid in the Treatment of Melasma and Sun-Induced Skin Hyperpigmentation. Cosmetics. 2022;9:108.

    Not in our library10.3390/cosmetics9050108

  39. 39.

    McKesey J., Tovar-Garza A., Pandya A.G. Melasma treatment: An evidence-based review. Am. J. Clin. Dermatol. 2020;21:173-225.

    Not in our library10.1007/s40257-019-00488-w

  40. 40.

    Grimes P.E., Ijaz S., Nashawati R., Kwak D. New oral and topical approaches for the treatment of melasma. Int. J. Women’s Dermatol. 2019;5:30-36.

    Not in our library10.1016/j.ijwd.2018.09.004

  41. 41.

    Artzi O., Horovitz T., Bar-Ilan E., Shehadeh W., Koren A., Zusmanovitch L., Mehrabi J., Salameh F., Nelkenbaum G.I., Zur E., et al. The pathogenesis of melasma and implications for treatment. J. Cosmet. Dermatol. 2021;20:3432-3445.

    Not in our library10.1111/jocd.14382

  42. 42.

    Taraz M., Niknam S., Ehsani A.H. Tranexamic acid in treatment of melasma: A comprehensive review of clinical studies. Dermatol. Ther. 2017;30:e12465.

    Not in our library10.1111/dth.12465

  43. 43.

    Tse T.W., Hui E. Tranexamic acid: An important adjuvant in the treatment of melasma. J. Cosmet. Dermatol. 2013;12:57-66.

    Not in our library10.1111/jocd.12026

  44. 44.

    Sharma R., Mahajan V.K., Mehta K.S., Chauhan P.S., Rawat R., Shiny T.N. Therapeutic efficacy and safety of oral tranexamic acid and that of tranexamic acid local infiltration with microinjections in patients with melasma: A comparative study. Clin. Exp. Dermatol. 2017;42:728-734.

    Not in our library10.1111/ced.13164

  45. 45.

    Kim S.J., Park J.Y., Shibata T., Fujiwara R., Kang H.Y. Efficacy and possible mechanisms of topical tranexamic acid in melasma. Clin. Exp. Dermatol. 2016;41:480-485.

    Not in our library10.1111/ced.12835

  46. 46.

    Sofen B., Prado G., Emer J. Melasma and post inflammatory hyperpigmentation: Management update and expert opinion. Skin. Ther. Lett. 2016;21:1-7.

    Not in our library

  47. 47.

    Demir B., Çiçek D., Bilik L., Aydoğdu E.G., Artaş H., Demirpolat N., Ergin C. Oral isotretinoin induced pigmentation disorder: A case report. Firat Tip Derg. 2017;22:143-145.

    Not in our library

  48. 48.

    Mysore V., Mahadevappa O.H., Barua S., Majid I., Viswanath V., Bhat R.M., Talwar S., Thurakkal S., Aurangabadkar S.J., Chatterjee M., et al. Standard guidelines of care: Performing procedures in patients on or recently administered with isotretinoin. J. Cutan. Aesthetic Surg. 2017;10:186-194.

    Not in our library10.4103/jcas.jcas_110_17

  49. 49.

    Bagatin E., Costa C.S. The use of isotretinoin for acne–an update on optimal dosing, surveillance, and adverse effects. Expert Rev. Clin. Pharmacol. 2020;13:885-897.

    Not in our library10.1080/17512433.2020.1796637

  50. 50.

    Fallah H., Rademaker M. Isotretinoin in the management of acne vulgaris: Practical prescribing. Int. J. Dermatol. 2021;60:451-460.

    Not in our library10.1111/ijd.15089

  51. 51.

    Villani A., Nastro F., Di Vico F., Fabbrocini G., Annunziata M.C., Genco L. Oral isotretinoin for acne: A complete overview. Expert Opin. Drug Saf. 2022;21:1027-1037.

    Not in our library10.1080/14740338.2022.2102605

  52. 52.

    Spring L.K., Krakowski A.C., Alam M., Bhatia A., Brauer J., Cohen J., Rosso J.Q., Diaz L., Dover J., Eichenfield L.F., et al. Isotretinoin and timing of procedural interventions: A systematic review with consensus recommendations. JAMA Dermatol. 2017;153:802-809.

    Not in our library10.1001/jamadermatol.2017.2077

  53. 53.

    Chu S., Michelle L., Ekelem C., Sung C.T., Rojek N., Mesinkovska N.A. Oral isotretinoin for the treatment of dermatologic conditions other than acne: A systematic review and discussion of future directions. Arch. Dermatol. Res. 2021;313:391-430.

    Not in our library10.1007/s00403-020-02152-4

  54. 54.

    Shao X., Chen Y., Zhang L., Zhang Y., Ariyawati A., Chen T., Chen J., Liu L., Pu Y., Li Y., et al. Effect of 30% supramolecular salicylic acid peel on skin microbiota and inflammation in patients with moderate-to-severe acne vulgaris. Dermatol. Ther. 2023;13:155-168.

    Not in our library10.1007/s13555-022-00844-5

  55. 55.

    Dréno B., Araviiskaia E., Kerob D., Andriessen A., Anfilova M., Arenbergerova M., Barrios L.O., Mokos Z.B., Haedersdal M., Hofmann M.A. Nonprescription acne vulgaris treatments: Their role in our treatment armamentarium—An international panel discussion. J. Cosmet. Dermatol. 2020;19:2201-2211.

    Not in our library10.1111/jocd.13497

  56. 56.

    Rachmin I., Ostrowski S.M., Weng Q.Y., Fisher D.E. Topical treatment strategies to manipulate human skin pigmentation. Adv. Drug Deliv. Rev. 2020;153:65-71.

    Not in our library10.1016/j.addr.2020.02.002

  57. 57.

    Bose S.K., Ortonne J.P. Pigmentation: Dyschromia. Textbook of Cosmetic Dermatology. 1998;391-415.

    Not in our library

  58. 58.

    Yasir M., Goyal A., Sonthalia S. Corticosteroid adverse effects. StatPearls. 2022.

    Not in our library

  59. 59.

    Yélamos O., Alejo B., Ertekin SSVilla-Crespo L., Zamora-Barquero S., Martinez N., Domínguez M., Iglesias P., Herrero A., Malvehy J., Puig S. Non-invasive clinical and microscopic evaluation of the response to treatment with clobetasol cream vs. calcipotriol/betamethasone dipropionate foam in mild to moderate plaque psoriasis: An investigator-initiated, phase IV, unicentric, open, randomized clinical trial. J. Eur. Acad. Dermatol. Venereol. 2021;35:143-149.

    Not in our library10.1111/jdv.16559

  60. 60.

    Cho J.H., Bhutani S., Kim C.H., Irwin M.R. Anti-inflammatory effects of melatonin: A systematic review and meta-analysis of clinical trials. Brain Behav. Immun. 2021;93:245-253.

    Not in our library10.1016/j.bbi.2021.01.034

  61. 61.

    Karekar S.R., Marathe P.A., Nagarajan V.B., Khopkar U.S., Chikhalkar S.B., Desai P.K., Dongre M.S. Use of topical steroids in dermatology: A questionnaire based study. Indian Dermatol. Online J. 2020;11:725-730.

    Not in our library10.4103/idoj.idoj_566_19

  62. 62.

    Chadderdon C., Gaston R.G., Loeffler B.J., Lewis D. Betamethasone Versus Ketorolac Injection for the Treatment of De Quervain’s Tenosynovitis: A Double-Blind Randomized Clinical Trial: Level 1 Evidence. J. Hand Surg. 2017;42:S45-S46.

    Not in our library10.1016/j.jhsa.2017.06.086

  63. 63.

    Patel H.K., Barot B.S., Parejiya P.B., Shelat P.K., Shukla A. Topical delivery of clobetasol propionate loaded microemulsion based gel for effective treatment of vitiligo: Ex vivo permeation and skin irritation studies. Colloids Surf. B Biointerfaces. 2013;102:86-94.

    Not in our library10.1016/j.colsurfb.2012.08.011

  64. 64.

    Khaitan B.K., Sindhuja T. Autoimmunity in vitiligo: Therapeutic implications and opportunities. Autoimmun. Rev. 2022;21:102932.

    Not in our library10.1016/j.autrev.2021.102932

  65. 65.

    Eleftheriadou V., Atkar R., Batchelor J., McDonald B., Novakovic L., Patel J.V., Ravenscroft J., Rush E., Shah D., Shah R., et al. British Association of Dermatologists’ Clinical Standards Unit. British Association of Dermatologists guidelines for the management of people with vitiligo 2021. Br. J. Dermatol. 2022;186:18-29.

    Not in our library10.1111/bjd.20596

  66. 66.

    Habet K.A., Kolli S.S., Pona A., Feldman S.R. A review of topical corticosteroid sprays for the treatment of inflammatory dermatoses. Dermatol. Online J. 2019;25:3-12.

    Not in our library10.5070/d3258045123

  67. 67.

    Gajinov Z. Corticosteroid topical therapy range: Fluocinolone-acetonide gel. Galen. Med. J. 2022;1:17-22.

    Not in our library10.5937/galmed2202017g

  68. 68.

    Medici S., Peana M., Nurchi V.M., Zoroddu M.A. Medical uses of silver: History, myths, and scientific evidence. J. Med. Chem. 2019;62:5923-5943.

    Not in our library10.1021/acs.jmedchem.8b01439

  69. 69.

    Bandyopadhyay D. Topical antibacterials in dermatology. Indian J. Dermatol. 2021;66:117-125.

    Not in our library10.4103/ijd.ijd_99_18

  70. 70.

    Adhya A., Bain J., Ray O., Hazra A., Adhikari S., Dutta G., Ray S., Majumdar B.K. Healing of burn wounds by topical treatment: A randomized controlled comparison between silver sulfadiazine and nano-crystalline silver. J. Basic Clin. Pharm. 2014;6:29-34.

    Not in our library10.4103/0976-0105.145776

  71. 71.

    Nethi S.K., Das S., Patra C.R., Mukherjee S. Recent advances in inorganic nanomaterials for wound-healing applications. Biomater. Sci. 2019;7:2652-2674.

    Not in our library10.1039/c9bm00423h

  72. 72.

    Srivastava S., Patil A., Prakash C., Kumari H. Comparison of intralesional triamcinolone acetonide, 5-fluorouracil, and their combination in treatment of keloids. World J. Plast. Surg. 2018;7:212-219.

    Not in our library10.1089/wound.2017.0741

  73. 73.

    Khan H.A., Sahibzada M.N., Paracha M.M. Comparison of the efficacy of intralesional bleomycin versus intralesional triamcinolone acetonide in the treatment of keloids. Dermatol. Ther. 2019;32:e13036-40.

    Not in our library10.1111/dth.13036

  74. 74.

    Raman P., Pitty R., Krithika C.L., Anand S.N., Subramani G.P. Topical curcumin and triamcinolone acetonide in recurrent minor aphthous ulcers: A pilot trial. J. Contemp. Dent. Pract. 2020;21:884-890.

    Not in our library

  75. 75.

    Kwiatkowska D., Wicka M., Bulska E., Kaliszewski P. Investigation of the Excretion of Triamcinolone Acetonide and Its Metabolite. Separations. 2023;10:164.

    Not in our library10.3390/separations10030164

  76. 76.

    Mangion S.E., Mackenzie L., Roberts M.S., Holmes A.M. Seborrheic dermatitis: Topical therapeutics and formulation design. Eur. J. Pharm. Biopharm. 2023;185:148-164.

    Not in our library10.1016/j.ejpb.2023.01.023

  77. 77.

    Pinto L.M., Chiricozzi A., Calabrese L., Mannino M., Peris K. Novel Therapeutic Strategies in the Topical Treatment of Atopic Dermatitis. Pharmaceutics. 2022;14:2767.

    Not in our library10.3390/pharmaceutics14122767

  78. 78.

    Sandhu S., Klein B.A., Al-Hadlaq M., Chirravur P., Bajonaid A., Xu Y., Intini R., Hussein M., Vacharotayangul P., Sroussi H., et al. Oral lichen planus: Comparative efficacy and treatment costs—A systematic review. BMC Oral Health. 2022;22:161.

    Not in our library10.1186/s12903-022-02168-4

  79. 79.

    Pakravan F., Ghalayani P., Emami H., Isfahani M.N., Noorshargh P. A novel formulation for radiotherapy-induced oral mucositis: Triamcinolone acetonide mucoadhesive film. J. Res. Med. Sci. Off. J. Isfahan Univ. Med. Sci. 2019;24:63.

    Not in our library10.4103/jrms.jrms_456_18

  80. 80.

    Mangold A.R., Pittelkow M.R. Lichen planus. Clin. Basic Immunodermatology. 2017;551-576.

    Not in our library10.1007/978-3-319-29785-9_31

  81. 81.

    Ahmad Nasrollahi S., Sabet Nematzadeh M., Samadi A., Ayatollahi A., Yadangi S., Abels C., Firooz A. Evaluation of the safety and efficacy of a triple combination cream (hydroquinone, tretinoin, and fluocinolone) for treatment of melasma in Middle Eastern skin. Clin. Cosmet. Investig. Dermatol. 2019;12:437-444.

    Not in our library10.2147/ccid.s202285

  82. 82.

    Dreher F., Draelos Z.D., Gold M.H., Goldman M.P., Fabi S.G., Puissegur Lupo M.L. Efficacy of hydroquinone-free skin-lightening cream for photoaging. J. Cosmet. Dermatol. 2013;12:12-17.

    Not in our library10.1111/jocd.12025

  83. 83.

    Banihashemi M., Zabolinejad N., Jaafari M.R., Salehi M., Jabari A. Comparison of therapeutic effects of liposomal tranexamic acid and conventional hydroquinone on melasma. J. Cosmet. Dermatol. 2015;14:174-177.

    Not in our library10.1111/jocd.12152

  84. 84.

    Pradhan M., Singh D., Murthy S.N., Singh M.R. Design, characterization and skin permeating potential of Fluocinolone acetonide loaded nanostructured lipid carriers for topical treatment of psoriasis. Steroids. 2015;101:56-63.

    Not in our library10.1016/j.steroids.2015.05.012

  85. 85.

    Treesirichod A., Chaithirayanon S., Chaikul T., Chansakulporn S. The randomized trials of 10% urea cream and 0.025% tretinoin cream in the treatment of acanthosis nigricans. J. Dermatol. Treat. 2021;32:837-842.

    Not in our library10.1080/09546634.2019.1708855

  86. 86.

    Bagatin E., Gonçalves H.D.S., Sato M., Almeida L.M.C., Miot H.A. Comparable efficacy of adapalene 0.3% gel and tretinoin 0.05% cream as treatment for cutaneous photoaging. Eur. J. Dermatol. 2018;28:343-350.

    Not in our library10.1684/ejd.2018.3320

  87. 87.

    Nautiyal A., Wairkar S. Management of hyperpigmentation: Current treatments and emerging therapies. Pigment Cell Melanoma Res. 2021;34:1000-1014.

    Not in our library10.1111/pcmr.12986

  88. 88.

    Ferraris C., Rimicci C., Garelli S., Ugazio E., Battaglia L. Nanosystems in cosmetic products: A brief overview of functional, market, regulatory and safety concerns. Pharmaceutics. 2021;13:1408.

    Not in our library10.3390/pharmaceutics13091408

  89. 89.

    Usatine R., Tinitigan M. Diagnosis and treatment of lichen planus. Am. Fam. Physician. 2011;84:53-60.

    Not in our library

  90. 90.

    Korabiusz K., Wawryków A., Fabian-Danielewska A., Stecko M., Wilczyńska A., Janik-Fuks I., Martyna M., Harasimowicz J. Laser removal of tattoo-A case report. J. Educ. Health Sport. 2019;9:415-419.

    Not in our library

  91. 91.

    Doucette K., Forster S., Marcus A. Study to Assess Visual Elimination of a Novel Otic Gel (Florfenicol, Terbinafine, Betamethasone Acetate) in Comparison to an Otic Solution (Florfenicol, Terbinafine, Mometasone Furoate) and an Otic Suspension (Gentamicin Sulfate, Clotrimazole, Mometasone Furoate Monohydrate) in Dogs Immediately after Application to the Ear Canal. BSAVA Congress Proceedings 2018. 2018;489.

    Not in our library

  92. 92.

    Grammatikova N.É. Comparative study of the antimicrobial activity of combined topical medicinal formulations of betamethasone, gentamicin, and clotrimazole in vitro. Pharm. Chem. J. 2020;53:971-975.

    Not in our library10.1007/s11094-020-02107-z

  93. 93.

    Cole L.K., Rajala-Schultz P.J., Lorch G. Conductive hearing loss in four dogs associated with the use of ointment-based otic medications. Vet. Dermatol. 2018;29:341-e120.

    Not in our library10.1111/vde.12542

  94. 94.

    Hikmatovich I.N. Evaluation of the Efficacy of External Therapy in Sick Children with Alergodermatosis. Web Semant. Univers. J. Innov. Educ. 2023;2:50-54.

    Not in our library

  95. 95.

    Harris J.E., Rashighi M., Nguyen N., Jabbari A., Ulerio G., Clynes R., Christiano A.M., Mackay-Wiggan J. Rapid skin repigmentation on oral ruxolitinib in a patient with coexistent vitiligo and alopecia areata (AA). J. Am. Acad. Dermatol. 2016;74:370-371.

    Not in our library10.1016/j.jaad.2015.09.073

  96. 96.

    Rosmarin D., Pandya A.G., Lebwohl M., Grimes P., Hamzavi I., Gottlieb A.B., Butler K., Kuo F., Sun K., Ji T., et al. Ruxolitinib cream for treatment of vitiligo: A randomised, controlled, phase 2 trial. Lancet. 2020;396:110-120.

    Not in our library10.1016/s0140-6736(20)30609-7

  97. 97.

    Rothstein B., Joshipura D., Saraiya A., Abdat R., Ashkar H., Turkowski Y., Vaneeta Sheth V., Huang V., Chung S., Kachuk C., et al. Treatment of vitiligo with the topical Janus kinase inhibitor ruxolitinib. J. Am. Acad. Dermatol. 2017;76:1054-1060.

    Not in our library10.1016/j.jaad.2017.02.049

  98. 98.

    Sheikh A., Rafique W., Owais R., Malik F., Ali E. FDA approves Ruxolitinib (Opzelura) for Vitiligo Therapy: A breakthrough in the field of dermatology. Ann. Med. Surg. 2022;81:104499-104506.

    Not in our library10.1016/j.amsu.2022.104499

  99. 99.

    Shreberk-Hassidim R., Ramot Y., Zlotogorski A. Janus kinase inhibitors in dermatology: A systematic review. J. Am. Acad. Dermatol. 2017;76:745-753.

    Not in our library10.1016/j.jaad.2016.12.004

  100. 100.

    Chapman S., Kwa M., Gold L.S., Lim H.W. Janus kinase inhibitors in dermatology: Part I. A comprehensive review. J. Am. Acad. Dermatol. 2022;86:406-413.

    Not in our library10.1016/j.jaad.2021.07.002

  101. 101.

    Rosmarin D., Passeron T., Pandya A.G., Grimes P., Harris J.E., Desai S.R., Lebwohl M., Mulard M., Seneschal J., Wolkerstorfer A., et al. Two phase 3, randomized, controlled trials of ruxolitinib cream for vitiligo. N. Engl. J. Med. 2022;387:1445-1455.

    Not in our library10.1056/nejmoa2118828

  102. 102.

    Seneschal J., Wolkerstorfer A., Desai S.R., Grimes P., Ezzedine K., Kornacki D., Butler K., Kuo F.I., Sun K., Grimes P., et al. Efficacy and safety of ruxolitinib cream for the treatment of vitiligo by patient demographics and baseline clinical characteristics: Week 52 pooled subgroup analysis from two randomized phase 3 studies. Br. J. Dermatol. 2023;188((Suppl. S1)):ljac106-006.

    Not in our library10.1093/bjd/ljac106.006

  103. 103.

    Sripathi S.K., Lalitha P. Keratolytic Molecule Aided Inhibition of DNA Damage and Tyrosinase Activity of a Herbal Formulation. Int. J. BioSci. Technol. 2016;9:7-14.

    Not in our library

  104. 104.

    Arif T. Salicylic acid as a peeling agent: A comprehensive review. Clin. Cosmet. Investig. Dermatol. 2015;8:455-461.

    Not in our library10.2147/ccid.s84765

  105. 105.

    Liu J., Jiang R., Zhou J., Xu X., Sun Z., Li J., Chen X., Li Z., Yan X., Zhao D., et al. Salicylic acid in ginseng root alleviates skin hyperpigmentation disorders by inhibiting melanogenesis and melanosome transport. Eur. J. Pharmacol. 2021;910:174458.

    Not in our library10.1016/j.ejphar.2021.174458

  106. 106.

    Karnes J.B., Usatine R.P. Management of external genital warts. Am. Fam. Physician. 2014;90:312-318.

    Not in our library

  107. 107.

    Lu J., Cong T., Wen X., Li X., Du D., He G., Jiang X. Salicylic acid treats acne vulgaris by suppressing AMPK/SREBP 1 pathway in sebocytes. Exp. Dermatol. 2019;28:786-794.

    Not in our library10.1111/exd.13934

  108. 108.

    Yeoh S.C., Goh C.F. Topical delivery of salicylates. Drug Deliv. Transl. Res. 2021;12:981-1001.

    Not in our library10.1007/s13346-021-00988-5

  109. 109.

    Ogbechie-Godec O.A., Elbuluk N. Melasma: An up-to-date comprehensive review. Dermatol. Ther. 2017;7:305-318.

    Not in our library10.1007/s13555-017-0194-1

  110. 110.

    Kaufman B.P., Aman T., Alexis A.F. Postinflammatory hyperpigmentation: Epidemiology, clinical presentation, pathogenesis and treatment. Am. J. Clin. Dermatol. 2018;19:489-503.

    Not in our library10.1007/s40257-017-0333-6

  111. 111.

    Al-Niaimi F., Chiang N.Y.Z. Topical vitamin C and the skin: Mechanisms of action and clinical applications. J. Clin. Aesthetic Dermatol. 2017;10:14-17.

    Not in our library

  112. 112.

    Ravetti S., Clemente C., Brignone S., Hergert L., Allemandi D., Palma S. Ascorbic acid in skin health. Cosmetics. 2019;6:58.

    Not in our library10.3390/cosmetics6040058

  113. 113.

    Goik U., Goik T., Załęska I. The properties and application of argan oil in cosmetology. Eur. J. Lipid Sci. Technol. 2019;121:1800313-1800342.

    Not in our library10.1002/ejlt.201800313

  114. 114.

    Phong C., Lee V., Yale K., Sung C., Mesinkovska N. Coconut, Castor, and Argan Oil for Hair in Skin of Color Patients: A Systematic Review. J. Drugs Dermatol. JDD. 2022;21:751-757.

    Not in our library10.36849/jdd.6972

  115. 115.

    Charrouf Z., Guillaume D. The argan oil project: Going from utopia to reality in 20 years. OCL. 2018;25:D209-D214.

    Not in our library10.1051/ocl/2018006

  116. 116.

    Kanlayavattanakul M., Lourith N. Plants and natural products for the treatment of skin hyperpigmentation–A review. Planta Med. 2018;84:988-1006.

    Not in our library10.1055/a-0583-0410

  117. 117.

    Hollinger J.C., Angra K., Halder R.M. Are natural ingredients effective in the management of hyperpigmentation? A systematic review. J. Clin. Aesthetic Dermatol. 2018;11:28-37.

    Not in our library

  118. 118.

    Panzella L., Napolitano A. Natural and bioinspired phenolic compounds as tyrosinase inhibitors for the treatment of skin hyperpigmentation: Recent advances. Cosmetics. 2019;6:57.

    Not in our library10.3390/cosmetics6040057

  119. 119.

    Grimes P., Bhawan J., Howell M., Desai S., Coryell E., Einziger M., Simpson A., Yaroshinsky A., McCraw T. Histopathological Changes Induced by Malassezin: A Novel Natural Microbiome Indole for Treatment of Facial Hyperpigmentation. J. Drugs Dermatol. JDD. 2022;21:141-145.

    Not in our library10.36849/jdd.6596

  120. 120.

    Karadas F., Erdoğan S., Kor D., Oto G., Uluman M. The effects of different types of antioxidants (Se, vitamin E and carotenoids) in broiler diets on the growth performance, skin pigmentation and liver and plasma antioxidant concentrations. Braz. J. Poult. Sci. 2016;18:101-116.

    Not in our library10.1590/18069061-2015-0155

  121. 121.

    Lucock M.D. The evolution of human skin pigmentation: A changing medley of vitamins, genetic variability, and UV radiation during human expansion. Am. J. Biol. Anthropol. 2023;180:252-271.

    Not in our library10.1002/ajpa.24564

  122. 122.

    Rembe J.D., Fromm-Dornieden C., Stuermer E.K. Effects of vitamin B complex and vitamin C on human skin cells: Is the perceived effect measurable? Adv. Skin Wound Care. 2018;31:225-233.

    Not in our library10.1097/01.asw.0000531351.85866.d9

  123. 123.

    Farzanfar S., Kouzekonan G.S., Mirjani R., Shekarchi B. Vitamin B12-loaded polycaprolacton/gelatin nanofibrous scaffold as potential wound care material. Biomed. Eng. Lett. 2020;10:547-554.

    Not in our library10.1007/s13534-020-00165-6

  124. 124.

    Vivcharenko V., Wojcik M., Przekora A. Cellular response to vitamin C-enriched chitosan/agarose film with potential application as artificial skin substitute for chronic wound treatment. Cells. 2020;9:1185.

    Not in our library10.3390/cells9051185

  125. 125.

    Barrios-Garay K., Toledano-Serrabona J., Gay-Escoda C., Sánchez-Garcés M.Á. Clinical effect of vitamin C supplementation on bone healing: A systematic review. Med. Oral Patol. Oral Y Cirugía Bucal. 2022;27:e205-e215.

    Not in our library10.4317/medoral.24944

  126. 126.

    Ahn K.Y., Song H.J., Kim D.C. Effect of alpha-tocopheryl acetate, retinyl palmitate, and phytantriol on hair protection. J. Appl. Biol. Chem. 2022;65:307-312.

    Not in our library10.3839/jabc.2022.039

  127. 127.

    Santos J.S., Tavares G.D., Barradas T.N. Vitamin E and derivatives in skin health promotion. Vitamin E in Health and Disease-Interactions, Diseases and Health Aspects. 2021.

    Not in our library

  128. 128.

    Putranti A.R., Primaharinastiti R., Hendradi E. Effectivity and physicochemical stability of nanostructured lipid carrier coenzyme Q10 in different ratio of lipid cetyl palmitate and alpha tocopheryl acetate as carrier. Asian J. Pharm. Clin. Res. 2017;10:146-152.

    Not in our library10.22159/ajpcr.2017.v10i2.14835

  129. 129.

    Panichakul T., Rodboon T., Suwannalert P., Tripetch C., Rungruang R., Boohuad N., Youdee P. Additive effect of a combination of Artocarpus lakoocha and Glycyrrhiza glabra extracts on tyrosinase inhibition in melanoma B16 cells. Pharmaceuticals. 2020;13:310.

    Not in our library10.3390/ph13100310

  130. 130.

    Gupta A.K., Pathak U., Medhi M., Mastinu A., Sikarwar M.S., Mishra P. Botanical, chemical and pharmacological properties of artocarpus lakoocha (monkey fruit): A review. Agric. Rev. 2020;41:305-316.

    Not in our library10.18805/ag.r-1989

  131. 131.

    Ullah S., Shoaib R., Khan S., Masood A. Phytochemicals; Targeted-Based Therapeutic Approaches for Pigmentation Disorders. Open Access Indones. J. Med. Rev. 2023;3:368-381.

    Not in our library10.37275/oaijmr.v3i2.287

  132. 132.

    Vaughn A.R., Clark A.K., Sivamani R.K., Shi V.Y. Natural oils for skin-barrier repair: Ancient compounds now backed by modern science. Am. J. Clin. Dermatol. 2018;19:103-117.

    Not in our library10.1007/s40257-017-0301-1

  133. 133.
    Essential Oils and Their Single Compounds in Cosmetics—A Critical Review · 2018
    Not checked
  134. 134.

    Ali S.A., Galgut J.M., Choudhary R.K. On the novel action of melanolysis by a leaf extract of Aloe vera and its active ingredient aloin, potent skin depigmenting agents. Planta Med. 2012;78:767-771.

    Not in our library10.1055/s-0031-1298406

  135. 135.

    Gad H.A., Roberts A., Hamzi S.H., Gad H.A., Touiss I., Altyar A.E., Kensara A.O., Ashour M.L. Jojoba Oil: An updated comprehensive review on chemistry, pharmaceutical uses, and toxicity. Polymers. 2021;13:1711.

    Not in our library10.3390/polym13111711

  136. 136.

    Matsumoto Y., Ma S., Tominaga T., Yokoyama K., Kitatani K., Horikawa K., Suzuki K. Acute effects of transdermal administration of jojoba oil on lipid metabolism in mice. Medicina. 2019;55:594.

    Not in our library10.3390/medicina55090594

  137. 137.

    Blaak J., Staib P. An updated review on efficacy and benefits of sweet almond, evening primrose and jojoba oils in skin care applications. Int. J. Cosmet. Sci. 2022;44:1-9.

    Not in our library10.1111/ics.12758

  138. 138.

    Sturtevant D., Lu S., Zhou Z.W., Shen Y., Wang S., Song J.M., Zhong J., Burks D.J., Yang Z.Q., Yang Q.Y., et al. The genome of jojoba (Simmondsia chinensis): A taxonomically isolated species that directs wax ester accumulation in its seeds. Sci. Adv. 2020;6:e3240-e3253.

    Not in our library10.1126/sciadv.aay3240

  139. 139.

    Nasr M., Abdel-Hamid S., Moftah N.H., Fadel M., Alyoussef A.A. Jojoba oil soft colloidal nanocarrier of a synthetic retinoid: Preparation, characterization and clinical efficacy in psoriatic patients. Curr. Drug Deliv. 2017;14:426-432.

    Not in our library10.2174/1567201813666160513132321

  140. 140.

    Sánchez M., Avhad M.R., Marchetti J.M., Martínez M., Aracil J. Jojoba oil: A state of the art review and future prospects. Energy Convers. Manag. 2016;129:293-304.

    Not in our library10.1016/j.enconman.2016.10.038

  141. 141.

    Manoharan S., Vishnupriya V., Gayathri R. Phytochemical analysis and in vitro antioxidant activity of jojoba oil. J. Pharm. Sci. Res. 2016;8:512-516.

    Not in our library

  142. 142.

    Leite C.D.S., Bonafé G.A., Carvalho Santos J., Martinez C.A.R., Ortega M.M., Ribeiro M.L. The anti-inflammatory properties of licorice (Glycyrrhiza glabra)-derived compounds in intestinal disorders. Int. J. Mol. Sci. 2022;23:4121.

    Not in our library10.3390/ijms23084121

  143. 143.

    Kwon Y.J., Son D.H., Chung T.H., Lee Y.J. A review of the pharmacological efficacy and safety of licorice root from corroborative clinical trial findings. J. Med. Food. 2020;23:12-20.

    Not in our library10.1089/jmf.2019.4459

  144. 144.

    Mohiuddin A.K. Skin lightening & management of hyperpigmentation. Pharma Sci. Anal. Res. J. 2019;2:180020-180068.

    Not in our library

  145. 145.

    Kimyon R.S., Liou Y.L., Schlarbaum J.P., Warshaw E.M. Allergic contact dermatitis to licorice root extract. Dermatitis®. 2019;30:227-228.

    Not in our library10.1097/der.0000000000000475

  146. 146.

    Spencer J.M., Accioly J., Kitchen N. Double Blind, Placebo Controlled Evaluation of a Novel Skin Lightening Agent. J. Drugs Dermatol. JDD. 2018;17:113-115.

    Not in our library

  147. 147.

    Dhariwala M.Y., Ravikumar P. An overview of herbal alternatives in androgenetic alopecia. J. Cosmet. Dermatol. 2019;18:966-975.

    Not in our library10.1111/jocd.12930

  148. 148.

    Boscariol R., Junior J.M.O., Baldo D.A., Balcão V.M., Vila M.M. Transdermal permeation of curcumin promoted by choline geranate ionic liquid: Potential for the treatment of skin diseases. Saudi Pharm. J. 2022;30:382-397.

    Not in our library10.1016/j.jsps.2022.01.023

  149. 149.

    Vo T.S., Vo T.T.B.C., Vo T.T.T.N., Lai T.N.H. Turmeric (Curcuma longa L.): Chemical components and their effective clinical applications. J. Turk. Chem. Soc. Sect. A Chem. 2021;8:883-898.

    Not in our library10.18596/jotcsa.913136

  150. 150.

    Firmansyah D., Sumiwi S.A., Saptarini N.M., Levita J. Curcuma longa extract inhibits the activity of mushroom tyrosinase and the growth of murine skin cancer B16F10 cells. J. Herbmed Pharmacol. 2023;12:153-158.

    Not in our library10.34172/jhp.2023.15

  151. 151.

    Farooqui R.K., Kaurav M., Kumar M., Sudheesh M.S., Pandey R.S. Permeation enhancer nanovesicles mediated topical delivery of curcumin for the treatment of hyperpigmentation. J. Liposome Res. 2022;32:332-339.

    Not in our library10.1080/08982104.2021.2024567

  152. 152.

    Akter J., Islam M.Z., Hossain M.A., Takara K. Anti-tyrosinase properties of different species of turmeric and isolation of active compounds from Curcuma amada. Med. Chem. Res. 2021;30:1669-1676.

    Not in our library10.1007/s00044-021-02764-z

  153. 153.

    Rodríguez-Cid L., Qian W., Iribarra-Araya J., Etcheverry-Berríos Á., Martínez-Olmos E., Choquesillo-Lazarte D., Sañudo E.C., Roubeau O., Periago A.M.L., González-Camp A., et al. Broadening the scope of high structural dimensionality nanomaterials using pyridine-based curcuminoids. Dalton Trans. 2021;50:7056-7064.

    Not in our library10.1039/d1dt00708d

  154. 154.

    Colantonio S., Rivers J.K. Botanicals with dermatologic properties derived from first nations healing: Part 2—Plants and algae. J. Cutan. Med. Surg. 2017;21:299-307.

    Not in our library10.1177/1203475416683390

  155. 155.

    Vaughn A.R., Clark A.K., Notay M., Sivamani R.K. Randomized controlled pilot study of dietary supplementation with turmeric or herbal combination tablets on skin barrier function in healthy subjects. J. Med. Food. 2018;21:1260-1265.

    Not in our library10.1089/jmf.2018.0015

  156. 156.

    Kallis P.J., Price A., Dosal J.R., Nichols A.J., Keri J. A Biologically Based Approach to Acne and Rosacea. J. Drugs Dermatol. JDD. 2018;17:611-617.

    Not in our library

  157. 157.

    Song X.C., Canellas E., Wrona M., Becerril R., Nerin C. Comparison of two antioxidant packaging based on rosemary oleoresin and green tea extract coated on polyethylene terephthalate for extending the shelf life of minced pork meat. Food Packag. Shelf Life. 2020;26:100588-100597.

    Not in our library10.1016/j.fpsl.2020.100588

  158. 158.

    Bagheri R., Rashidlamir A., Ashtary-Larky D., Wong A., Alipour M., Motevalli M.S., Chebbi A., Laher I., Zouhal H. Does green tea extract enhance the anti-inflammatory effects of exercise on fat loss? Br. J. Clin. Pharmacol. 2020;86:753-762.

    Not in our library10.1111/bcp.14176

  159. 159.

    Gaweł-Bęben K., Kukula-Koch W., Hoian U., Czop M., Strzępek-Gomółka M., Antosiewicz B. Characterization of Cistus× incanus L. and Cistus ladanifer L. extracts as potential multifunctional antioxidant ingredients for skin protecting cosmetics. Antioxidants. 2020;9:202.

    Not in our library10.3390/antiox9030202

  160. 160.

    Tang G., Xu Y., Zhang C., Wang N., Li H., Feng Y. Green tea and epigallocatechin gallate (EGCG) for the management of nonalcoholic fatty liver diseases (NAFLD): Insights into the role of oxidative stress and antioxidant mechanism. Antioxidants. 2021;10:1076.

    Not in our library10.3390/antiox10071076

  161. 161.

    Hodges J.K., Sasaki G.Y., Bruno R.S. Anti-inflammatory activities of green tea catechins along the gut–liver axis in nonalcoholic fatty liver disease: Lessons learned from preclinical and human studies. J. Nutr. Biochem. 2020;85:108478-108524.

    Not in our library10.1016/j.jnutbio.2020.108478

  162. 162.

    Chaikul P., Sripisut T., Chanpirom S., Ditthawutthikul N. Anti-skin aging activities of green tea (Camelliasinensis (L) Kuntze) in B16F10 melanoma cells and human skin fibroblasts. Eur. J. Integr. Med. 2020;40:101212-101240.

    Not in our library10.1016/j.eujim.2020.101212

  163. 163.

    Bhattacharya S., Sherje A.P. Development of resveratrol and green tea sunscreen formulation for combined photoprotective and antioxidant properties. J. Drug Deliv. Sci. Technol. 2020;60:102000-102023.

    Not in our library10.1016/j.jddst.2020.102000

  164. 164.

    Winkelman W.J. Aromatherapy, botanicals, and essential oils in acne. Clin. Dermatol. 2018;36:299-305.

    Not in our library10.1016/j.clindermatol.2018.03.004

  165. 165.

    Patidar K. Unmet Need and Challenges of Skin Aging by Herbal Anti-aging Cosmeceuticals: An Overview. Asian J. Pharm. (AJP). 2018;12:410-418.

    Not in our library

  166. 166.

    Phasha V., Senabe J., Ndzotoyi P., Okole B., Fouche G., Chuturgoon A. Review on the use of kojic acid—A skin-lightening ingredient. Cosmetics. 2022;9:64.

    Not in our library10.3390/cosmetics9030064

  167. 167.

    Saeedi M., Eslamifar M., Khezri K. Kojic acid applications in cosmetic and pharmaceutical preparations. Biomed. Pharmacother. 2019;110:582-593.

    Not in our library10.1016/j.biopha.2018.12.006

  168. 168.

    Khezri K., Saeedi M., Morteza-Semnani K., Akbari J., Hedayatizadeh-Omran A. A promising and effective platform for delivering hydrophilic depigmenting agents in the treatment of cutaneous hyperpigmentation: Kojic acid nanostructured lipid carrier. Artif. Cells Nanomed. Biotechnol. 2021;49:38-47.

    Not in our library10.1080/21691401.2020.1865993

  169. 169.

    Khan A., Park T.J., Ikram M., Ahmad S., Ahmad R., Jo M.G., Kim M.O. Antioxidative and Anti-inflammatory Effects of Kojic Acid in Aβ-Induced Mouse Model of Alzheimer’s Disease. Mol. Neurobiol. 2021;58:5127-5140.

    Not in our library10.1007/s12035-021-02460-4

  170. 170.

    Zilles J.C., Dos Santos F.L., Kulkamp-Guerreiro I.C., Contri R.V. Biological activities and safety data of kojic acid and its derivatives: A review. Exp. Dermatol. 2022;31:1500-1521.

    Not in our library10.1111/exd.14662

  171. 171.

    Bakhouche I., Aliat T., Boubellouta T., Gali L., Şen A., Bellik Y. Phenolic contents and in vitro antioxidant, anti-tyrosinase, and anti-inflammatory effects of leaves and roots extracts of the halophyte Limonium delicatulum. S. Afr. J. Bot. 2021;139:42-49.

    Not in our library10.1016/j.sajb.2021.01.030

  172. 172.

    Li T.X., Liang J.X., Liu L.L., Shi F.C., Jia X.W., Li M.H., Xu C.P. Novel kojic acid derivatives with anti-inflammatory effects from Aspergillus versicolor. Fitoterapia. 2021;154:105027-105033.

    Not in our library10.1016/j.fitote.2021.105027

  173. 173.

    Gust P.J., Luke J.D. Kojic acid. J. Dermatol. Nurses’ Assoc. 2016;8:338-340.

    Not in our library10.1097/jdn.0000000000000247

  174. 174.

    Searle T., Al-Niaimi F., Ali F.R. The top 10 cosmeceuticals for facial hyperpigmentation. Dermatol. Ther. 2020;33:e14095-e14139.

    Not in our library10.1111/dth.14095

  175. 175.

    Ohno Y., Kondo S., Tajima K., Shibata T., Itoh T. Effect of phlorotannins isolated from Eisenia bicyclis on melanogenesis in mouse B16 melanoma cells. Nat. Prod. Commun. 2021;16:1934578X211019264.

    Not in our library10.1177/1934578x211019264

  176. 176.

    Phang S.J., Teh H.X., Looi M.L., Arumugam B., Fauzi M.B., Kuppusamy U.R. Phlorotannins from brown algae: A review on their antioxidant mechanisms and applications in oxidative stress-mediated diseases. J. Appl. Phycol. 2023;35:867-892.

    Not in our library10.1007/s10811-023-02913-4

  177. 177.

    Jesumani V., Du H., Aslam M., Pei P., Huang N. Potential use of seaweed bioactive compounds in skincare—A review. Mar. Drugs. 2019;17:688.

    Not in our library10.3390/md17120688

  178. 178.

    Zhao W., Yang A., Wang J., Huang D., Deng Y., Zhang X., Qu Q., Ma W., Xiong R., Zhu M., et al. Potential application of natural bioactive compounds as skin-whitening agents: A review. J. Cosmet. Dermatol. 2022;21:6669-6687.

    Not in our library10.1111/jocd.15437

  179. 179.

    Kim K.N., Yang H.M., Kang S.M., Ahn G., Roh S.W., Lee W., Kim D.K., Jeon Y.J. Whitening effect of octaphlorethol A isolated from Ishige foliacea in an in vivo zebrafish model. J. Microbiol. Biotechnol. 2015;25:448-451.

    Not in our library10.4014/jmb.1409.09033

  180. 180.

    Lee S.H., Kang N., Kim E.A., Heo S.J., Moon S.H., Jeon B.T., Jeon Y.J. Antidiabetogenic and antioxidative effects of octaphlorethol a isolated from the brown algae Ishige foliacea in streptozotocin-induced diabetic mice. Food Sci. Biotechnol. 2014;23:1261-1266.

    Not in our library10.1007/s10068-014-0173-6

  181. 181.

    Thawabteh A.M., Swaileh Z., Ammar M., Jaghama W., Yousef M., Karaman R., Bufo S.A., Scrano L. Antifungal and Antibacterial Activities of Isolated Marine Compounds. Toxins. 2023;15:93.

    Not in our library10.3390/toxins15020093

  182. 182.

    Shanura Fernando I.P., Asanka Sanjeewa K.K., Samarakoon K.W., Kim H.S., Gunasekara U.K.D.S.S., Park Y.J., Abeytunga D.T.U., Lee W.W., Jeon Y.J. The potential of fucoidans from Chnoospora minima and Sargassum polycystum in cosmetics: Antioxidant, anti-inflammatory, skin-whitening, and antiwrinkle activities. J. Appl. Phycol. 2018;30:3223-3232.

    Not in our library10.1007/s10811-018-1415-4

  183. 183.

    Kok J.M.L., Jee J.M., Chew L.Y., Wong C.L. The potential of the brown seaweed Sargassum polycystum against acne vulgaris. J. Appl. Phycol. 2016;28:3127-3133.

    Not in our library10.1007/s10811-016-0825-4

  184. 184.

    Lourenço-Lopes C., Fraga-Corral M., Soria-Lopez A., Nuñes-Estevez B., Barral-Martinez M., Silva A., Li N., Liu C., Gandara J.S., Prieto M.A. Fucoxanthin’s optimization from Undaria pinnatifida using conventional heat extraction, bioactivity assays and in silico studies. Antioxidants. 2022;11:1296.

    Not in our library10.3390/antiox11071296

  185. 185.

    Park E.J., Choi J.I. Melanogenesis inhibitory effect of low molecular weight fucoidan from Undaria pinnatifida. J. Appl. Phycol. 2017;29:2213-2217.

    Not in our library10.1007/s10811-016-1048-4

  186. 186.

    Lee S.H., Kang S.M., Ko S.C., Lee D.H., Jeon Y.J. Octaphlorethol A, a novel phenolic compound isolated from a brown alga, Ishige foliacea, increases glucose transporter 4-mediated glucose uptake in skeletal muscle cells. Biochem. Biophys. Res. Commun. 2012;420:576-581.

    Not in our library10.1016/j.bbrc.2012.03.036

  187. 187.

    Lajis A.F.B., Ariff A.B. Discovery of new depigmenting compounds and their efficacy to treat hyperpigmentation: Evidence from in vitro study. J. Cosmet. Dermatol. 2019;18:703-727.

    Not in our library10.1111/jocd.12900

  188. 188.

    Haggag Y.A., Abd Elrahman A.A., Ulber R., Zayed A. Fucoidan in pharmaceutical formulations: A comprehensive review for smart drug delivery systems. Mar. Drugs. 2023;21:112.

    Not in our library10.3390/md21020112

  189. 189.

    Guan B., Chen K., Tong Z., Chen L., Chen Q., Su J. Advances in fucoxanthin research for the prevention and treatment of inflammation-related diseases. Nutrients. 2022;14:4768.

    Not in our library10.3390/nu14224768

  190. 190.

    Natsume C., Aoki N., Aoyama T., Senda K., Matsui M., Ikegami A., Tanaka K., Azuma Y.T., Fujita T. Fucoxanthin ameliorates atopic dermatitis symptoms by regulating keratinocytes and regulatory innate lymphoid cells. Int. J. Mol. Sci. 2020;21:2180.

    Not in our library10.3390/ijms21062180

  191. 191.

    Garcia-Jimenez A., Teruel-Puche J.A., Berna J., Rodriguez-Lopez J.N., Tudela J., Garcia-Ruiz P.A., Garcia-Canovas F. Characterization of the action of tyrosinase on resorcinols. Bioorg. Med. Chem. 2016;24:4434-4443.

    Not in our library10.1016/j.bmc.2016.07.048

  192. 192.

    Jin Y.J., Lin C.C., Lu T.M., Li J.H., Chen I.S., Kuo Y.H., Ko H.H. Chemical constituents derived from Artocarpus xanthocarpus as inhibitors of melanin biosynthesis. Phytochemistry. 2015;117:424-435.

    Not in our library10.1016/j.phytochem.2015.07.003

  193. 193.

    Yamahara M., Sugimura K., Kumagai A., Fuchino H., Kuroi A., Kagawa M., Itoh Y., Kawahara H., Nagaoka Y., Iida O., et al. Callicarpa longissima extract, carnosol-rich, potently inhibits melanogenesis in B16F10 melanoma cells. J. Nat. Med. 2016;70:28-35.

    Not in our library10.1007/s11418-015-0933-5

  194. 194.

    Mustapha N., Bzéouich I.M., Ghedira K., Hennebelle T., Chekir-Ghedira L. Compounds isolated from the aerial part of Crataegus azarolus inhibit growth of B16F10 melanoma cells and exert a potent inhibition of the melanin synthesis. Biomed. Pharmacother. 2015;69:139-144.

    Not in our library10.1016/j.biopha.2014.11.010

  195. 195.

    Nam J.H., Nam D.Y., Lee D.U. Valencene from the rhizomes of Cyperus rotundus inhibits skin photoaging-related ion channels and UV-induced melanogenesis in B16F10 melanoma cells. J. Nat. Prod. 2016;79:1091-1096.

    Not in our library10.1021/acs.jnatprod.5b01127

  196. 196.

    Jin K.S., Lee J.Y., Hyun S.K., Kim B.W., Kwon H.J. Juniperus chinensis and the functional compounds, cedrol and widdrol, ameliorate α-melanocyte stimulating hormone-induced melanin formation in B16F10 cells. Food Sci. Biotechnol. 2015;24:611-618.

    Not in our library10.1007/s10068-015-0080-5

  197. 197.

    de Freitas M.M., Fontes P.R., Souza P.M., William Fagg C., Neves Silva Guerra E., de Medeiros Nobrega Y.K., Silveira D., Bazzo Y.F., Simeoni L.A., Homem-de-Mello M., et al. Extracts of Morus nigra L. leaves standardized in chlorogenic acid, rutin and isoquercitrin: Tyrosinase inhibition and cytotoxicity. PLoS ONE. 2016;11:e0163130-e0163154.

    Not in our library10.1371/journal.pone.0163130

  198. 198.

    Kanlayavattanakul M., Lourith N., Chaikul P. Jasmine rice panicle: A safe and efficient natural ingredient for skin aging treatments. J. Ethnopharmacol. 2016;193:607-616.

    Not in our library10.1016/j.jep.2016.10.013

  199. 199.

    Lourith N., Kanlayavattanakul M., Chingunpitak J. Development of sunscreen products containing passion fruit seed extract. Braz. J. Pharm. Sci. 2017;53:1-8.

    Not in our library10.1590/s2175-97902017000116116

  200. 200.

    Sallam A., Mira A., Ashour A., Shimizu K. Acetylcholine esterase inhibitors and melanin synthesis inhibitors from Salvia officinalis. Phytomedicine. 2016;23:1005-1011.

    Not in our library10.1016/j.phymed.2016.06.014

  201. 201.

    Srisayam M., Weerapreeyakul N., Barusrux S., Kanokmedhakul K. Antioxidant, antimelanogenic, and skin-protective effect of sesamol. J. Cosmet Sci. 2014;65:69-79.

    Not in our library

  202. 202.

    Diwakar G., Rana J., Saito L., Vredeveld D., Zemaitis D., Scholten J. Inhibitory effect of a novel combination of Salvia hispanica (chia) seed and Punica granatum (pomegranate) fruit extracts on melanin production. Fitoterapia. 2014;97:164-171.

    Not in our library10.1016/j.fitote.2014.05.021

  203. 203.

    Lourith N., Kanlayavattanakul M., Chaikul P., Chansriniyom C., Bunwatcharaphansakun P. In vitro and cellular activities of the selected fruits residues for skin aging treatment. An. Acad. Bras. Ciências. 2017;89:577-589.

    Not in our library10.1590/0001-3765201720160849

  204. 204.

    Patel P.D., Mohan G.C., Bhattacharya T., Patel R.A., Tsoukas M. Pediatric laser therapy in pigmented conditions. Am. J. Clin. Dermatol. 2019;20:647-655.

    Not in our library10.1007/s40257-019-00449-3

  205. 205.

    Xie X.Y., Fu G.L., Yang Q., Zeng Y., Ke H., Lu J.J., Yi H. Clinical Efficacy of 755 nm Laser Treatment of Lip Mucosal Pigmentation in Children with Peutz–Jeghers Syndrome. Dermatol. Ther. 2023;2023:8020443-8020447.

    Not in our library10.1155/2023/8020443

  206. 206.

    Nunez J.H., Strong A.L., Comish P., Hespe G.E., Harvey J., Sorkin M., Levi B. A Review of Laser Therapies for the Treatment of Scarring and Vascular Anomalies. Adv. Wound Care. 2023;12:68-84.

    Not in our library10.1089/wound.2021.0045

  207. 207.

    Purohit S.J., Tharmavaram M., Rawtani D., Prajapati P., Pandya H., Dey A. Niosomes as cutting edge nanocarrier for controlled and targeted delivery of essential oils and biomolecules. J. Drug Deliv. Sci. Technol. 2022;73:103438.

    Not in our library10.1016/j.jddst.2022.103438

  208. 208.

    Sharma S., Vashist S., Lamba A.K., Arora S. Novel Strategies in the Treatment of Acne: A Review. Int. J. Pharm. Investig. 2022;12:123-128.

    Not in our library10.5530/ijpi.2022.2.23

  209. 209.

    Yonekawa Y., Thomas B.J., Thanos A., Todorich B., Drenser K.A., Trese M.T., Capone Jr A. The cutting edge of retinopathy of prematurity care: Expanding the boundaries of diagnosis and treatment. Retina. 2017;37:2208-2225.

    Not in our library10.1097/iae.0000000000001719

  210. 210.

    Al Qarqaz F., Al-Yousef A. Skin microneedling for acne scars associated with pigmentation in patients with dark skin. J. Cosmet. Dermatol. 2018;17:390-395.

    Not in our library10.1111/jocd.12520

  211. 211.

    Ziaeifar E., Ziaeifar F., Mozafarpoor S., Goodarzi A. Applications of microneedling for various dermatologic indications with a special focus on pigmentary disorders: A comprehensive review study. Dermatol. Ther. 2021;34:e151-e159.

    Not in our library10.1111/dth.15159

  212. 212.

    Lima E.V.A., Lima M.M.D.A., Miot H.A. Induction of pigmentation through microneedling in stable localized vitiligo patients. Dermatol. Surg. 2020;46:434-435.

    Not in our library10.1097/dss.0000000000001846

  213. 213.

    Ahmed N.A., Mohammed S.S., Fatani M.I. Treatment of periorbital dark circles: Comparative study of carboxy therapy vs chemical peeling vs mesotherapy. J. Cosmet. Dermatol. 2019;18:169-175.

    Not in our library10.1111/jocd.12536

  214. 214.

    Sarkar R., Arsiwala S., Dubey N., Sonthalia S., Das A., Arya L., Gokhale N., Torsekar R.G., Somani V.K., Majid I., et al. Chemical peels in melasma: A review with consensus recommendations by Indian pigmentary expert group. Indian J. Dermatol. 2017;62:578-584.

    Not in our library10.4103/ijd.ijd_490_17

  215. 215.

    Kadry M., Tawfik A., Abdallah N., Badawi A., Shokeir H. Platelet-rich plasma versus combined fractional carbon dioxide laser with platelet-rich plasma in the treatment of vitiligo: A comparative study. Clin. Cosmet. Investig. Dermatol. 2018;11:551-559.

    Not in our library10.2147/ccid.s178817

  216. 216.

    Mohamad N.E., ELgameel R.M., Mohamed M.H. Comparative study between the effectiveness of plasma skin regeneration versus micro-needling in the treatment of striae distensae. J. Cosmet. Dermatol. 2022;21:4545-4553.

    Not in our library10.1111/jocd.14751

  217. 217.

    Wulandari P., Jusuf N.K., Nasution K. Microneedling and platelet-rich plasma (PRP) treatment for mixed melasma. J. Gen. Proced. Dermatol. Venereol. Indones. 2022;6:44.

    Not in our library10.19100/jdvi.v6i1.303

  218. 218.

    Rezapour A., Arabloo J., Moradi N., Ehsanzadeh S.J., Hourzad M., Alipour V. Safety and effectiveness of endodermal radiofrequency for skin rejuvenation: A systematic review. Aesthetic Plast. Surg. 2023;47:378-386.

    Not in our library10.1007/s00266-022-03097-x

  219. 219.

    Goel A., Gatne V. Use of nanofractional radiofrequency for the treatment of acne scars in Indian skin. J. Cosmet. Dermatol. 2017;16:186-192.

    Not in our library10.1111/jocd.12311

Reads

Read by people on this page

None yet.

Checked or read by AI through naulon

None yet.

A person counts once a day per paper. We keep no cookie and no address: a reader is a hash that changes every day. Any month under five reads shows no number.

Are you an author?

Is this your paper?

Claim it to add your note and be paid when agents cite it. Free.