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Skin Delivery of Kojic Acid-loaded Nanotechnology-based Drug Delivery Systems for the Treatment of Skin Aging

Overview
Journal Biomed Res Int
Publisher Wiley
Date 2013 Dec 26
PMID 24369010
Citations 14
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Abstract

The aging process causes a number of changes in the skin, including oxidative stress and dyschromia. The kojic acid (KA) is iron chelator employed in treatment of skin aging, and inhibits tyrosinase, promotes depigmentation. Nanotechnology-based drug delivery systems, such as liquid crystalline systems (LCSs), can modulate drug permeation through the skin and improve the drug activity. This study is aimed at structurally developing and characterizing a kojic acid-loaded LCS, consists of water (W), cetostearyl isononanoate (oil-O) and PPG-5-CETETH-20 (surfactant-S) and evaluating its in vitro skin permeation and retention. Three regions of the diagram were selected for characterization: A (35% O, 50% S, 15% W), B (30% O, 50% S, 20% W) and C (20% O, 50% S, 30% W), to which 2% KA was added. The formulations were subjected to polarized light microscopy, which indicated the presence of a hexagonal mesophase. Texture and bioadhesion assay showed that formulation B is suitable for topical application. According to the results from the in vitro permeation and retention of KA, the formulations developed can modulate the permeation of KA in the skin. The in vitro cytotoxic assays showed that KA-unloaded LCS and KA-loaded LCS didn't present cytotoxicity. PPG-5-CETETH-20-based systems may be a promising platform for KA skin delivery.

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References
1.
Mukherjee P, Maity N, Nema N, Sarkar B . Bioactive compounds from natural resources against skin aging. Phytomedicine. 2011; 19(1):64-73. DOI: 10.1016/j.phymed.2011.10.003. View

2.
Aronson H . Correction factor for dissolution profile calculations. J Pharm Sci. 1993; 82(11):1190. DOI: 10.1002/jps.2600821126. View

3.
Chen L, Hu J, Wang S . The role of antioxidants in photoprotection: a critical review. J Am Acad Dermatol. 2012; 67(5):1013-24. DOI: 10.1016/j.jaad.2012.02.009. View

4.
Lajis A, Hamid M, Ariff A . Depigmenting effect of Kojic acid esters in hyperpigmented B16F1 melanoma cells. J Biomed Biotechnol. 2012; 2012:952452. PMC: 3468271. DOI: 10.1155/2012/952452. View

5.
Chorilli M, Prestes P, Rigon R, Leonardi G, Chiavacci L, Sarmento V . Structural characterization and in vivo evaluation of retinyl palmitate in non-ionic lamellar liquid crystalline system. Colloids Surf B Biointerfaces. 2011; 85(2):182-8. DOI: 10.1016/j.colsurfb.2011.02.027. View