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Extraction, Structural Characterization, and Biological Functions of Lycium Barbarum Polysaccharides: A Review

Xiaojing Tian, Tisong Liang, Yuanlin Liu and 3 more

Biomolecules · 2019 · Review · CC BY

doi:10.3390/biom9090389

Abstract

Lycium barbarum polysaccharides (LBPs), as bioactive compounds extracted from L. barbarum L. fruit, have been widely explored for their potential health properties. The extraction and structural characterization methods of LBPs were reviewed to accurately understand the extraction method and structural and biological functions of LBPs. An overview of the biological functions of LBPs, such as antioxidant function, antitumor activity, neuroprotective effects, immune regulating function, and other functions, were summarized. This review provides an overview of LBPs and a theoretical basis for further studying and extending the applications of LBPs in the fields of medicine and food.

Full text

From PubMed Central, U.S. National Library of Medicine, as current on Oct 20, 2026. Paragraph numbers are ours, so an answer can point at one.

1. Introduction

Lycium barbarum L., known as the wolfberry or goji berry, the fruits derived from Lycium barbarum L, are a local food that is widely distributed in the arid and semi-arid regions of China, Korea, Japan, Europe, North America, and the Mediterranean. Currently, China is the largest world producer with its 82,000 ha of cultivated land and 95,000 t of berries produced per year. The earliest use of the goji berry as a medicinal plant was at around 2300 years ago. L. barbarum L. fruit is used as a traditional Chinese herbal medicine and functional food in daily life.

Three Lycium species (L. barbarum, L. chinense, and L. ruthenicum) have been discovered. Among the three species, the yield of Lycium barbarum is the largest in China. They are used as medicine in China and as medicinal and functional food because of their health benefits, including anti-aging, antioxidant, antidiabetic, anticancer, cytoprotective, neuroprotective, and immunomodulatory effects. The physical appearance of Lycium barbarum is shown in Figure 1. The fruit is red and about 1–2 cm long. Numerous reports have been conducted to explore the function and characterization of its extracts because of the health benefits of Lycium barbarum. More than 200 different components, including carotenoids, phenylpropanoids, flavonoids, polyphenols, and polysaccharides, have been identified, characterized, and analyzed. Polysaccharides, vitamins, betaine, and mixed extracts of the goji berry are responsible for health benefits, such as eliciting anti-aging effects, improving eyesight, and exhibiting antifatigue effects.

Among Lycium barbarum extracts, L. barbarum polysaccharides (LBPs) isolated from L. barbarum fruit have been responsible for the biological activities of Lycium barbarum. LBPs are a group of water-soluble glycoconjugates with a molecular weight of 10–2300 kDa and comprise 5–8% of the dried fruits. The beneficial health effects of LBPs, including antioxidant and antiaging effects, increased metabolism, antiglaucoma effects, immune regulation, anticancer effects, neuroprotective properties, and antidiabetic effects, have been reported. According to the Chinese understanding of Lycium extracts and products, the content of LBPs is important for the efficacy of L. barbarum. Therefore, as bioactive constituents of L. barbarum, LBPs have many biological functions to improve people’s health. The biological functions of LBPs are complex and multifaceted because of the relationship between the physiological structure and functions of LBPs. The relationship and mechanism between LBPs and human health should be fully understood. In order to give a comprehensive understanding of LBPS, the extraction methods, structure, composition, and biological functions of LBPs were summarized and discussed in this review. We collected and summarized the relative contents from previous reports to provide a theory basis for comprehensively understanding and utilizing LBPs in medical and food fields.

2. Extraction Methods of LBPs

Previous reports have shown that the chemical ingredients of L. barbarum fruit include polysaccharides, proteins, and phenylpropanoids. Among these ingredients, LBPs account for 5–8% of the dried fruit and elicit biological effects. LBPs are subjected to extraction, purification, and analysis. The flowchart of the extraction, purification, and analysis of LBPs is shown in Figure 2.

LBPs are extracted by destroying and degrading the cell wall under mild conditions without changing the properties of the polysaccharides in accordance with basic extraction principles. Many LBP extraction methods, such as the water extraction method, enzyme-assisted extraction method, microwave-assisted extraction method, ultrasonic-assisted extraction method, and supercritical fluid extraction method, have been developed on the basis of this principle. Traditional LBP extraction methods have some advantages and disadvantages. Novel LBP extraction technologies, such as ultrasound-assisted extraction method (UAE), enzyme-assisted extraction method (EAM), microwave-assisted extraction method (MAM), and supercritical fluid extraction method (SFM), have been developed to address the disadvantages of traditional extraction methods. The high extraction yield and high biological activity of LBPs are considered in choosing an extraction method.

These extraction methods have unique strengths and weaknesses. Hot water extraction (HWE) is the traditional method for polysaccharide extraction. The yield of HWE is largely affected by extraction time, temperature, and the ratio of water to raw material. Also, the long duration and high temperature may lead to the degradation of the polysaccharides and decrease their biological activity. EAM possesses the advantages of environmental friendliness, high efficiency, ease of operation, and low investment cost and energy. However, the enzyme is characterized by specificity and selectivity, while several factors, such as enzyme concentration, temperature, time, and pH also affect the biological function of polysaccharides. MAM is a physical technique that is used for the extraction of polysaccharides. MAE has noticeable advantages, such as shorter extraction time, higher extraction yield, lower cost, and less solvent consumption. UAM has the advantage of improving penetration and capillary effects, leading to an increase of polysaccharides’ extractability. However, ultrasonic treatment could affect the structure and molecular weight (MW) of polysaccharides, which would cause a change in the biological activity. The extraction conditions and yield of LBP extract by different extraction methods are shown in Table 1.

As the traditional extraction method is widely used in the extraction of LBPs, the yield of the water extraction method (WEM) is 5.87% under the experimental conditions. The yields of LBPs via UAM, EAM, and MAM are 2.286–5.701%, 6.81% ± 0.10%, and 8.25% ± 0.07%, respectively. The yield of LBPs of novel extraction methods is higher than that of the water extraction method. Moreover, the combination of different extraction methods can obtain enhanced yields of LBPs; when the ultrasound-enhanced subcritical water extraction method (USWE) is used to extract the LBPs, high recovery yields of LBPs are produced.

3. Structure and Composition of LBPs

The separation and structural characterization methods of purified LBPs have been developed. As active ingredients, LBPs possess various biological functions. More than 33 polysaccharides have been analyzed and identified from L. barbarum L.

The main applied and performance techniques for the structural characterization of LBP fraction include the following techniques: (1) high-performance gel permeation chromatography (HPGPC), which is used to determine the homogeneity and molecular weight of macromolecules; (2) partial acid or enzymatic hydrolysis, oxidation with periodic acid, Smith degradation, high-performance liquid chromatography (HPLC), gas chromatography (GC), polysaccharide analysis by gel electrophoresis (PACE), and high-performance thin-layer chromatography (HPTLC). These techniques are used to determine monosaccharide composition and map the glycidic component of glycoconjugates; (3) infrared (IR) spectral analysis permits the identification of pyranosyl or furanosyl ring form and α or β anomeric configuration in monosaccharide residues; (4) 1H and 13C nuclear magnetic resonance (NMR) spectroscopy used to assign the ratios of monosaccharides present and ratios of their anomeric bonds; (5) gas chromatography–mass spectrometry (GC–MS), employed to determine the linkage positions.

Studies have widely explored the structure and composition of LBPs and demonstrated that LBPs are polysaccharides, including some ingredients of acidic heteropolysaccharides, polypeptides, or proteins. The molecular weight of LBPs at the range of 10–2300 kDa. The methods used for the isolation and purification of LBPs from L. barbarum include DEAE ion-exchange cellulose, gel-permeation chromatography, and high-performance liquid chromatography (HPLC). About 20 types of polysaccharides, including Rha, Fuc, Ara, Gal, and GalA, have been investigated. Studies have shown that monosaccharide and amino acid residues constitute glycoconjugates, and, relative to glycosidic linkage analysis of glycan backbone, branching sites and side chains were considered as the structure of LBPs. The possible structure of repeat units, molecular weights, and analysis technique of previously investigated polysaccharides in L. barbarum are shown in Table 2.

4.1. Antioxidant Function

Natural bioactive compounds present good biological activities, such as antioxidant, anticancer, and other functions, because of the broad diversity of structures and functionalities. As bioactive compounds, LBPs have good antioxidant properties. Antioxidant activity is mainly contributed by carotenoids, flavonoids, ascorbic acid and its derivatives, and polyphenols.

The biological function of LBPs have many potential functions relative to the antioxidant activity in many tissues. Studies have investigated the antioxidant activity of LBPs that extract with hot water and the protective effect of LBPs against tissue oxidative injury, with results showing that LBPs exhibit a good antioxidant activity and a protective effect against skin oxidative injury. The antioxidant effects of LBPs extracted by hot water have been explored via an in vivo model, showing that LBP treatments can significant increase the serum levels of SOD and GSH-Px and significantly decrease MDA contents. The antioxidant function of LBPs shows that LBPs can significantly enhance macrophage NO, phagocytic capacity, and acid phosphatase, and exhibit good antioxidant activities in vitro. LBPs can significantly increase cell viability that decreases by LPS and regulate oxidative stress by inhibiting caspase-3 activation and ROS levels in vitro. Studies have investigated the effects of LBPs on stressed RPE cells and have shown that LBPs can decrease ROS levels via free radical scavenging and downstream gene function to prevent ROS-induced apoptosis. Antioxidant enzyme activities, GSH levels, and MDA levels in rats fed with a high-fat diet and LBPs decreased when compared with those in the control group (p < 0.01). The antioxidant activity and mechanisms of LBPs are shown in Table 3.

4.2. Immune Regulation

Immune regulation is an important function of LBPs in people’s health. Previous studies have shown that LBPs exhibit an immune-modulating function in target dendritic cells, macrophages, T- and B-lymphocytes, and natural killer (NK) cells. The immune regulation of LBPs is an important function that has been studied widely in previous studies.

Dendritic cells are used to study the effects of LBPs, and results have shown that LBPs can induce the phenotypic and functional maturation of DCs via Notch signaling and promote the cytotoxicity of DC-mediated CTLs. In nutritive additives, LBPs can be used as an additive in the growth of broilers, indicating that LBPs may possess the clinical efficacy for growth promotion and immunomodulation and can be used as an alternative to nutritive additive in broilers. The nanoliposome technique is used to load LBPs and study their function, showing that LBPs can significantly promote splenocyte proliferation, increase the amount of CD4(+) to CD8(+) T cells, and promote the cytokine secretion of macrophages. The extract of L. barbarum exhibits a significant immunomodulatory activity through the promotion effects of nitric oxide and cytokines in RAW264.7 cells. The efficacies of sulfated LBPs on immune enhancements in cultured chicken are high. In summary, the immune regulation and mechanism of LBPs are shown in Table 4.

4.3. Antitumor Activity of LBPs

The antitumor activity of natural products isolated from plants have been reported. Previous studies have shown that more than 100 polysaccharides exhibit good anticancer activity via in vitro studies and in vivo animal models.

As natural products, LBPs exhibit potential antitumor activity. Studies have shown that the anticancer activity of LBPs occurs because of their effects on cancer tissue or cancer cells. The exposure to hot water extracts of Lycium barbarum for 24 h made cell viability reduce to 15.31% of hepatocellular carcinoma cells, as reported in a previous study. Colorectal cancer is one of the most common cancers worldwide, with a study showing that the treatment of LBP (5000 mg/L) can decrease cell viability of SW480 and Caco-2 cells to 10% after 5 days of treatment, and that the treatment with LBP resulted in a dose-dependent increase in the distribution of cells in the G0/G1 phase. For gastric cancer cells, LBPs can inhibit the proliferation of these cells and arrest the cell cycle at the G0/G1 phase, suggesting that LBPs are candidate anticancer agents. The inhibitory effect of LBPs on the growth of glioma in rats and the underlying mechanism have been explored, and results have shown that the mechanism may be related to the regulation of the blood–brain barrier and to the promotion of CD[8]+ T cell invasion in the brain. Studies on the effects of LBPs on the viability, cell cycle, and apoptosis of human hepatoma cells have demonstrated that LBPs can inhibit cell growth, arrest the cell cycle in the S phase, and induce apoptosis, suggesting the antiproliferative activity of LBPs by inducing cell cycle arrest and increasing intracellular calcium in the apoptotic system. The anticancer activity of LBPs is mainly due to the inhibited growth of cells, arrested cell cycle, and induced cell apoptosis. The antitumor activities of LBPs on different cancer cells are shown in Table 5. LBPs exhibit a good antitumor activity on various cancer cells.

These results show that LBPs can decrease the viability of cancer cells and have inhibitory effects on cancer cells, indicating that LBPs can be used as a candidate anticancer agent in cancer treatment.

4.4. Neuroprotective Effects of LBPs

Natural products isolated from plants exhibit certain biological functions and have been extensively investigated because of their efficiency and biosafety. As such, they have been widely used to treat diseases. Plant extracts have been utilized to treat various functions of central nervous systems. Polysaccharides are effective compounds from neurobiologically active plants, and many studies have demonstrated their beneficial effects, including neurological disorders.

The neuroprotective effects of LBPs on ischemic injury is mainly through the signaling pathways of NR2A activation and NR2B inhibition, and LBPs can be used to treat ischemic stroke. A mouse experiment model of the neuroprotective effects of LBPs have shown that LBPs may exert neuroprotective effects and help prevent neurodegenerative diseases. In modern society, visual impairments and blindness cause heavy damage on people’s health. LBP treatment can significantly weaken these injuries with enhanced endogenous autophagy in the body. The neuroprotective effects and molecular mechanisms of LBPs are shown in Table 6.

4.5. Other Biological Activities

The antioxidant activity, antitumor properties, immune regulation, and neuroprotective effects of LBPs were explored in in vitro and in vivo models. Besides this, LBPs also have other biological activities, such as protecting the liver from hepatotoxicity, alleviating dry-eye disease, eliciting antidiabetic effects, increasing cell abilities, decreasing cell morphologic impairment, protecting against ultraviolet-induced damage, and alleviating CCl4-induced liver fibrosis. As bioactive constituents, LBPs exhibit various biological functions and show potential benefits to people’s health. The other biological activities and mechanism of LBPs are summarized in Table 7.

5. Conclusions

In China, goji berries are a traditional medicinal herb that have been used for thousand years to cure disease and improve the function of the liver, kidney, and lungs. More recently, western countries have also started cultivating Lycium barbarum L. plants, whose fruits are consumed fresh or dried. Previous reports have showed that L. barbarum fruit exhibits a wide array of pharmacological activities. This beneficial L. barbarum component consists of a complex mixture of glycoconjugates—these being LBPs—with a molecular weight range of 10–2300 kDa, water solubility, and containing a carbohydrate portion (≥90%), represented by highly-branched polysaccharides. The LBP glycan backbones have been found to be mainly represented by α-(1→4)-galA, α-(1→6)-glc, β-(1→3)-galp (typical of arabinogalactan proteins), and β-(1→6)-galp. Other structures, less representative, are α-(1→5)-ara and β-(1→4)-galp, with different branching and terminal sites. The extraction methods of LBPs, including water extraction, enzyme-assisted extraction, microwave-assisted extraction, and ultrasonic-assisted extraction, produce different effects on the quality of LBPs. The biological functions of LBPs indicate that LBPs exhibits antioxidant, immunomodulation, antitumor, neuroprotection, and hepatoprotection.

LBPs are the main active substances in L. barbarum fruits and are involved in various biological functions. LBPs have great potential health benefits for further use in nutraceutical and pharmaceutical fields. The biological function of LBPs has been explored using in vitro and in vivo models but not in the human body. However, the relationship between a high-order LBP structure and bioactivities has yet to be further explored. Novel omics technologies, such as proteomics, metabolomics, and genomics, are effective in investigating the biological function of LBPs. Future works should focus on the high-order structures of LBPs, their biological function in the human body, and the relationship between their structure and bioactivity to enhance our understanding of the functional effects of LBPs. Current extraction methods give low yields and other weaknesses in the extraction of LBPs. Novel environmentally friendly and high-yielding extraction methods of LBPs should be further developed. The extraction methods and structural and biological functions of LBPs were summarized in this review to provide a useful bibliography for further investigations and applications of LBPs in medicine and food.

References 128

  1. 1.

    Li X.M. Protective effect of Lycium barbarum polysaccharides on streptozotocin-induced oxidative stress in rats. Int. J. Biol. Macromol. 2007;40:461-465.

    Not in our library10.1016/j.ijbiomac.2006.11.002

  2. 2.

    Amagase H., Farnsworth N.R. A review of botanical characteristics, phytochemistry, clinical relevance in efficacy and safety of Lycium barbarum fruit (Goji). Food Res. Int. 2011;44:1702-1717.

    Not in our library10.1016/j.foodres.2011.03.027

  3. 3.

    Wu D.-T., Guo H., Lin S., Lam S.-C., Zhao L., Lin D.-R., Qin W. Review of the structural characterization, quality evaluation, and industrial application of Lycium barbarum polysaccharides. Trends Food Sci. Technol. 2018;79:171-183.

    Not in our library10.1016/j.tifs.2018.07.016

  4. 4.

    Potterat O. Goji (Lycium barbarum and L. chinense): Phytochemistry, Pharmacology and Safety in the Perspective of Traditional Uses and Recent Popularity. Planta Med. 2010;76:7-19.

    Not in our library10.1055/s-0029-1186218

  5. 5.

    Wang H., Li J., Tao W., Zhang X., Gao X., Yong J., Zhao J., Zhang L., Li Y., Duan J.-A. Lycium ruthenicum studies: Molecular biology, Phytochemistry and pharmacology. Food Chem. 2018;240:759-766.

    Not in our library10.1016/j.foodchem.2017.08.026

  6. 6.

    Zeng S., Liu Y., Wu M., Liu X., Shen X., Liu C., Wang Y. Identification and validation of reference genes for quantitative real-time PCR normalization and its applications in lyceum. PLoS ONE. 2014;9:e97039.

    Not in our library10.1371/journal.pone.0097039

  7. 7.

    Wawruszak A., Czerwonka A., Okła K., Rzeski W. Anticancer effect of ethanol Lycium barbarum (Goji berry) extract on human breast cancer T47D cell line. Nat. Prod. Res. 2015;30:1.

    Not in our library10.1080/14786419.2015.1101691

  8. 8.

    Tang W.-M., Chan E., Kwok C.-Y., Lee Y.-K., Wu J.-H., Wan C.-W., Chan R.Y.-K., Yu P.H.-F., Chan S.-W. A review of the anticancer and immunomodulatory effects of Lycium barbarum fruit. Inflammopharmacology. 2012;20:307-314.

    Not in our library10.1007/s10787-011-0107-3

  9. 9.

    Zhang Q.Y., Chen W.W., Zhao J.H., Xi W.P. Functional constituents and antioxidant activities of eight Chinese native goji genotypes. Food Chem. 2016;200:230-236.

    Not in our library10.1016/j.foodchem.2016.01.046

  10. 10.

    Yao R., Heinrich M., Weckerle C.S. The genus Lycium as food and medicine: A botanical, ethnobotanical and historical review. J. Ethnopharmacol. 2018;212:50-66.

    Not in our library10.1016/j.jep.2017.10.010

  11. 11.

    Wang Q., Chen S., Zhang Z. Determination of Polysaccharide Contents in Fructus Lycii. Chin. Herbal Med. 1991;22:67-69.

    Not in our library

  12. 12.

    Lu S.-P., Zhao P.-T. Chemical characterization of Lycium barbarum polysaccharides and their reducing myocardial injury in ischemia/reperfusion of rat heart. Int. J. Biol. Macromol. 2010;47:681-684.

    Not in our library10.1016/j.ijbiomac.2010.08.016

  13. 13.

    Xin Y.-F., Wan L.-L., Peng J.-L., Guo C. Alleviation of the acute doxorubicin-induced cardiotoxicity by Lycium barbarum polysaccharides through the suppression of oxidative stress. Food Chem. Toxicol. 2011;49:259-264.

    Not in our library10.1016/j.fct.2010.10.028

  14. 14.
  15. 15.

    Gong H., Shen P., Jin L., Xing C., Tang F. Therapeutic effects of Lycium barbarum polysaccharide (LBP) on irradiation or chemotherapy-induced myelosuppressive mice. Cancer Biother. Radiopharm. 2005;20:155-162.

    Not in our library10.1089/cbr.2005.20.155

  16. 16.

    Chang R.C.-C., So K.-F. Use of anti-aging herbal medicine, Lycium barbarum, against aging-associated diseases. What do we know so far? Cell. Mol. Neurobiol. 2008;28:643-652.

    Not in our library10.1007/s10571-007-9181-x

  17. 17.

    He N., Yang X., Jiao Y., Tian L., Zhao Y. Characterisation of antioxidant and antiproliferative acidic polysaccharides from Chinese wolfberry fruits. Food Chem. 2012;133:978-989.

    Not in our library10.1016/j.foodchem.2012.02.018

  18. 18.

    Xiao J., Liong E.C., Ching Y.P., Chang R.C., So K.F., Fung M.L., Tipoe G.L. Lycium barbarum polysaccharides protect mice liver from carbon tetrachloride-induced oxidative stress and necroinflammation. J. Ethnopharmacol. 2012;139:462-470.

    Not in our library10.1016/j.jep.2011.11.033

  19. 19.

    Zhou Z.Q., Fan H.X., He R.R., Xiao J., Tsoi B., Lan K.H., Kurihara H., So K.F., Yao X.S., Gao H. Lycibarbarspermidines A–O, New Dicaffeoylspermidine Derivatives from Wolfberry, with Activities against Alzheimer’s Disease and Oxidation. J. Agric. Food Chem. 2016;64:2223.

    Not in our library10.1021/acs.jafc.5b05274

  20. 20.

    Zhang M., Cui S.W., Cheung P.C.K., Wang Q. Antitumor polysaccharides from mushrooms: a review on their isolation process, structural characteristics and antitumor activity. Trends Food Sci. Technol. 2007;18:4-19.

    Not in our library10.1016/j.tifs.2006.07.013

  21. 21.
  22. 22.

    Masci A., Carradori S., Casadei M.A., Paolicelli P., Petralito S., Ragno R., Cesa S. Lycium barbarum polysaccharides: Extraction, purification, structural characterisation and evidence about hypoglycaemic and hypolipidaemic effects. A review. Food Chem. 2018;254:377-389.

    Not in our library10.1016/j.foodchem.2018.01.176

  23. 23.

    Skenderidis P., Petrotos K., Giavasis I., Hadjichristodoulou C., Tsakalof A. Optimization of ultrasound assisted extraction of of goji berry (Lycium barbarum) fruits and evaluation of extracts’ bioactivity. J. Food Process. Eng. 2017;40:12.

    Not in our library10.1111/jfpe.12522

  24. 24.

    Zhao C., Yang R.F., Qiu T.Q. Ultrasound-enhanced subcritical water extraction of polysaccharides from Lycium barbarum L. Sep. Purif. Technol. 2013;120:141-147.

    Not in our library

  25. 25.

    Zhang J., Jia S.Y., Liu Y., Wu S.H., Ran J.Y. Optimization of enzyme-assisted extraction of the Lycium barbarum polysaccharides using response surface methodology. Carbohydr. Polym. 2011;86:1089-1092.

    Not in our library10.1016/j.carbpol.2011.06.027

  26. 26.

    Liu Z.G., Dang J., Wang Q.L., Yu M.F., Jiang L., Mei L.J., Shao Y., Tao Y.D. Optimization of polysaccharides from Lycium ruthenicum fruit using RSM and its anti-oxidant activity. Int. J. Biol. Macromol. 2013;61:127-134.

    Not in our library10.1016/j.ijbiomac.2013.06.042

  27. 27.

    Reverchon E., de Marco I. Supercritical fluid extraction and fractionation of natural matter. J. Supercrit. Fluids. 2006;38:146-166.

    Not in our library10.1016/j.supflu.2006.03.020

  28. 28.

    Ma T., Sun X., Tian C., Luo J., Zheng C., Zhan J. Polysaccharide extraction from Sphallerocarpus gracilis roots by response surface methodology. Int. J. Biol. Macromol. 2016;88:162-170.

    Not in our library10.1016/j.ijbiomac.2016.03.058

  29. 29.

    Zhong-Qiua H.U., Liu J.D., Wang B.L. Research on extraction technology of Lycium barbarum polysaccharides by the alkaline solution. J. Northwest A F Univ. Nat. Sci. Ed. 2008;36:173-178.

    Not in our library

  30. 30.

    Luo Q., Yan J., Zhang S. Isolation and purification of Lycium barbarum polysaccharides and its antifatigue effect. J. Hyg. Res. 2000;29:115-117.

    Not in our library

  31. 31.

    Ji X.L., Peng Q., Yuan Y.P., Liu F., Wang M. Extraction and physicochemical properties of polysaccharides from Ziziphus Jujuba cv. Muzao by ultrasound-assisted aqueous two-phase extraction. Int. J. Biol. Macromol. 2018;108:541-549.

    Not in our library10.1016/j.ijbiomac.2017.12.042

  32. 32.

    Yin G.H., Dang Y.L. Optimization of extraction technology of the Lycium barbarum polysaccharides by Box-Behnken statistical design. Carbohydr. Polym. 2008;74:603-610.

    Not in our library10.1016/j.carbpol.2008.04.025

  33. 33.

    Liu Y., Gong G., Zhang J., Jia S., Li F., Wang Y., Wu S. Response surface optimization of ultrasound-assisted enzymatic extraction polysaccharides from Lycium barbarum. Carbohydr. Polym. 2014;110:278-284.

    Not in our library10.1016/j.carbpol.2014.03.040

  34. 34.

    Yang R.-F., Zhao C., Chen X., Chan S.-W., Wu J.-Y. Chemical properties and bioactivities of Goji (Lycium barbarum) polysaccharides extracted by different methods. J. Funct. Foods. 2015;17:903-909.

    Not in our library10.1016/j.jff.2015.06.045

  35. 35.

    Li X.M., Li X.L., Zhou A.G. Evaluation of antioxidant activity of the polysaccharides extracted from Lycium barbarum fruits in vitro. Eur. Polym. J. 2007;43:488-497.

    Not in our library10.1016/j.eurpolymj.2006.10.025

  36. 36.

    Muatasim R., Ma H.L., Yang X. Effect of multimode ultrasound assisted extraction on the yield of crude polysaccharides from Lycium Barbarum (Goji). Food Sci. Technol. 2018;38:160-166.

    Not in our library10.1590/1678-457x.14417

  37. 37.

    Gao Z., Ali Z., Khan I.A. Glycerogalactolipids from the fruit of Lycium barbarum. Phytochemistry. 2008;69:2856-2861.

    Not in our library10.1016/j.phytochem.2008.09.002

  38. 38.

    Ouyang H.X., Li Y.Q., Xiao Q.W. Simultaneous determination of monosaccharides and oligosaccharides in Lycium barbarum L. by high performance liquid chromatography. Sichuan Da Xue Xue Bao. Yi Xue Ban = J. Sichuan Univ. Med. Sci. Ed. 2007;38:1040.

    Not in our library

  39. 39.

    Yang J., Wei Y.Q., Ding J.B., Li Y.L., Ma J.L., Liu J.L. Research and application of Lycii Fructus in medicinal field. Chin. Herb. Med. 2018;10:339-352.

    Not in our library10.1016/j.chmed.2018.08.006

  40. 40.

    Peng X., Tian G. Structural characterization of the glycan part of glycoconjugate LbGp2 from Lycium barbarum L. Carbohydr. Res. 2001;331:95-99.

    Not in our library10.1016/s0008-6215(00)00321-9

All 128 references

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