IN VITRO PENETRATION TESTS OF TRANSETHOSOME GEL PREPARATIONS CONTAINING CAPSAICIN
DOI:
https://doi.org/10.22159/ijap.2017.v9s1.68_75Keywords:
Capsaicin, Franz diffusion cell, Gel, Penetration, TransethosomeAbstract
Objective: Capsaicin is an active compound found in chili pepper and has been shown to have analgesic, antioxidant, anticancer, and anti-obesity
properties. To improve its penetration into the skin, capsaicin was prepared in a transethosome vesicle. Importantly, transethosomes are vesicles that
consist of phosphatidylcholine, surfactant, and ethanol. In this study, capsaicin was prepared in a transethosome vesicle using two different methods:
Direct transethosome formation and thin layer hydration. The aims of this study were to determine the effects of various methods of transethosome
formation on capsaicin characteristics and to evaluate the penetration capabilities of transethosome capsaicin gel.
Methods: Ultimately, transethosome formation via the thin layer method yielded more favorable characteristics; these formations had particle sizes
of 174.9±2.02 nm and an entrapment efficiency of 84.85±1.15%. The transethosome suspension was then developed into a gel formulation using 1%
carbomer. An in vitro penetration test was performed using a Franz diffusion cell of mice abdomen skin, and the performance of the transethosome
capsaicin gel was compared to that of the standard capsaicin gel.
Results: Penetration rate of capsaicin from either the transethosome gel preparation and the standard gel substance was 1549.68±49.6 and
846.05±10.1 μg/cm2, respectively.
Conclusions: According to these results, it can be concluded that gel preparations containing transethosome increase capsaicin penetration into the
skin.
Downloads
References
Kimura H, Ogawa S, Sugiyama A, Jisaka M, Takeuchi T, Yokota K.
Anti-obesity effects of highly polymeric proanthocyanidins from seed
shells of Japanese horse chestnut (Aesculus turbinata Blume). Food Res
Int 2011;44(1):121-6.
Whiting S, Derbyshire E, Tiwari BK. Capsaicinoids and capsinoids.
A potential role for weight management? A systematic review of the
evidence. Appetite 2012;59(2):341-8.
Sarwa KK, Mazumder B, Rudrapal M, Verma VK. Potential
of capsaicin-loaded transfersomes in arthritic rats. Drug Deliv
;22(22):638-46.
Ascenso A, Raposo S, Batista C, Cardoso P, Mendes T, Praça FG,
et al. Development, characterization, and skin delivery studies of
related ultradeformable vesicles: Transfersomes, ethosomes, and
transethosomes. Int J Nanomedicine 2015;10:5837-1.
Song CK, Balakrishnan P, Shim CK, Chung SJ, Chong S, Kim DD.
A novel vesicular carrier, transethosome, for enhanced skin delivery of
voriconazole: Characterization and in vitro/in vivo evaluation. Colloids
Surf B Biointerfaces 2012;92:299-304.
Ma M, Wang J, Guo F, Lei M, Tan F, Li N. Development of
nanovesicular systems for dermal imiquimod delivery: Physicochemical
characterization and in vitro/in vivo evaluation. J Mater Sci Mater Med
;26(6):191.
Shaji J, Garude S. Transethosomes and ethosomes for enhanced
transdermal delivery of ketorolac tromethamine. Comp Assess
;6(4):1-6.
A Guidebook to Particle Size Analysis. Available from: https://www.
horiba.com/fileadmin/uploads/Scientific/Documents/PSA/PSA_
Guidebook.pdf; 2014.
Chen Y, Wu Q, Zhang Z, Yuan L, Liu X, Zhou L. Preparation of
curcumin-loaded liposomes and evaluation of their skin permeation and
pharmacodynamics. Molecules 2012;17(5):5972-87.
El Zaafarany GM, Awad GA, Holayel SM, Mortada ND. Role of edge
activators and surface charge in developing ultradeformable vesicles
with enhanced skin delivery. Int J Pharm 2010;397(1-2):164-72.
Tranggoono RI, Latifah F. Handbook of Cosmetics Study. Jakarta:
Gramedia; 2007.
Barry BW. Novel mechanisms and devices to enable successful
transdermal drug delivery. Eur J Pharm Sci 2001;14(2):101-4.