Novel transethosome coencapsulated combination for acne treatment: in-vitro efficacy and ex-vivo biodistribution studies.

IF 1.8 4区 医学 Q3 DERMATOLOGY
Alfredo Martinez-Gutierrez, Javier Sendros, Teresa Noya, Mari C González
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引用次数: 0

Abstract

Background: Acne vulgaris is a skin condition affecting approximately 85% of young adults. It is influenced by androgens and primarily occurs in the pilosebaceous unit, where inflammation and obstruction happen. Hyperseborrhea and hyperkeratinization lead to increased levels of fatty acids and necrotic keratinocytes, promoting the proliferation of C. acnes phylotype IA1.

Methods: Here, the in-vitro efficacy of a novel combination on the main processes involved in acne was studied. Furthermore, the combination was coencapsulated in transethosomes to target the pilosebaceous unit, and the biodistribution was analyzed ex vivo by fluorescence microscopy.

Results: The combination of compounds reduced inflammatory markers levels, sebum production and 5α-Reductase levels while it induced autophagy and FOXO1 nuclear levels in sebocytes. The compounds coencapsulated in transethosomes reached the pilosebaceous unit as proven by the ex vivo analysis.

Conclusions: The proposed combination of compounds is a promising approach to be included in topical products for the treatment of acne vulgaris.

新型转酶体共包合治疗痤疮:体外疗效和体外生物分布研究。
背景:寻常性痤疮是一种影响大约85%年轻人的皮肤状况。它受雄激素的影响,主要发生在皮脂腺单位,那里发生炎症和阻塞。脂溢性分泌和角化过度导致脂肪酸和坏死角化细胞水平升高,促进痤疮C. IA1型的增殖。方法:本文研究了一种新型复方药物对痤疮主要过程的体外疗效。此外,将该组合物共包被在transsethosomes中以毛囊皮脂腺单位为靶点,并通过荧光显微镜分析其在体外的生物分布。结果:化合物联合使用可降低炎症标志物水平、皮脂生成和5α-还原酶水平,同时诱导自噬和皮脂细胞FOXO1核水平。经离体分析证实,这些共包被在脂质体中的化合物到达毛囊皮脂腺单位。结论:提出的化合物组合是一种有希望的方法,包括在外用产品治疗寻常性痤疮。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.10
自引率
0.00%
发文量
442
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