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Azelaic acid-based lyotropic liquid crystals gel for acne vulgaris: Formulation optimization, antimicrobial activity and dermatopharmacokinetic study.
- Source :
-
International journal of pharmaceutics [Int J Pharm] 2024 Dec 25; Vol. 667 (Pt A), pp. 124879. Date of Electronic Publication: 2024 Oct 28. - Publication Year :
- 2024
-
Abstract
- The proposed study aimed to develop a topical gel containing azelaic acid (AZA)-based lyotropic liquid crystals (LLCs) for the treatment of acne vulgaris. AZA-based LLCs were optimized by varying Poloxamer-407 and polyvinyl alcohol concentration using a central composite design, which showed that both independent variables had a significant effect on the formulation. The highest desirable trial of AZA-based LLCs (Batch-7) containing 300 mg poloxamer-407 and 100 mg polyvinyl alcohol depicted the particle size, zeta potential, and entrapment efficiency of 184.2 nm, -16.1 mV, and 79.96 %, respectively. TEM images confirmed the globular vesicles of LLCs, and ATR-FTIR and DSC results confirmed the compatibility of formulation excipients. In vitro, the release of AZA, AZA-based LLCs, AZA-based LLC gel, and marketed gel showed a release of 23.29, 95.24, 91.07 and 59.88 %, respectively, after 24 h in phosphate buffer pH 6.8. Ex vivo release of AZA-based LLC gel displayed an 86.56 % release after 24 h. The antimicrobial activity of AZA-based LLC gel exhibited a comparable efficacy with marketed gel against Cutibacterium acnes, Staphylococcus epidermis and Staphylococcus aureus. The acute dermal irritation study indicated excellent safety and skin compatibility of AZA-based LLC gel without any erythema and edema. The dermatopharmacokinetic study displayed an enhanced drug retention for AZA-based LLC gel (146.121 ± 21.13 µg/cm <superscript>2</superscript> ) than marketed gel (58.58 ± 15.95 µg/cm <superscript>2</superscript> ) in the dermal layer, which would improve its therapeutic effect. These outcomes proved that AZA-based LLC gel has the potential to enhance skin penetration and retention for effective management of acne vulgaris.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Drug Liberation
Skin metabolism
Male
Skin Absorption
Poloxamer chemistry
Particle Size
Administration, Cutaneous
Rabbits
Chemistry, Pharmaceutical methods
Staphylococcus aureus drug effects
Anti-Bacterial Agents administration & dosage
Anti-Bacterial Agents pharmacology
Anti-Bacterial Agents chemistry
Anti-Bacterial Agents pharmacokinetics
Drug Compounding
Excipients chemistry
Propionibacterium acnes drug effects
Acne Vulgaris drug therapy
Dicarboxylic Acids chemistry
Dicarboxylic Acids administration & dosage
Dicarboxylic Acids pharmacokinetics
Gels
Liquid Crystals chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1873-3476
- Volume :
- 667
- Issue :
- Pt A
- Database :
- MEDLINE
- Journal :
- International journal of pharmaceutics
- Publication Type :
- Academic Journal
- Accession number :
- 39490554
- Full Text :
- https://doi.org/10.1016/j.ijpharm.2024.124879