Topical Delivery of Meloxicam using Liposome and Microemulsion Formulation Approaches
Julia Zhang, Anna Froelich, Bozena Michniak-Kohn
Pharmaceutics · 2020
doi:10.3390/pharmaceutics12030282 (opens in a new tab)
We email you when a new notice or a question about this paper appears.
Abstract
The aim of this study is to develop, characterize and compare conventional liposome, deformable liposome (transfersome) and microemulsion formulations as potential topical delivery systems for meloxicam. Liposomes were characterized in terms of vesicle size, zeta potential and entrapment efficiency. For microemulsions, particle size, electrical conductivity and viscosity studies were performed to assess the structure of the investigated systems. An ex vivo skin permeation study has been conducted to compare these formulations. The dermal and transdermal delivery of meloxicam using these formulations can be a promising alternative to conventional oral delivery of non-steroidal anti-inflammatory drugs (NSAIDs) with enhanced local and systemic onset of action and reduced side effects.
Abstract licence: CC BY
References66
- 4.
39 more references, whose wording the paper’s licence keeps private.
All 66 referencesReads
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.