Invasomes: A vesicular carrier for transdermal delivery

Varenya S Sarangamath, E. Gopinath, J. Adlin, Jino Nesalin, V. Chandy
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Abstract

The transdermal route serves as a crucial pathway for delivering localized or systemic medications. Recognizing the skin's significance as a vital organ, it is imperative to develop effective strategies for drug delivery through this route. Invasomes represent a novel vesicular system that has shown superior transdermal penetration compared to traditional liposomes. Comprising phospholipids, ethanol, and terpene, invasomes exhibit suitable transdermal penetration properties for soft vesicles. These nanovesicles enhance drug permeability into the epidermis while minimizing systemic absorption, thereby confining drug action within the skin subcaste. In comparison to liposomes and ethosomes, invasomes penetrate deeper into the skin. They offer various advantages, including enhancing medication efficacy, improving patient compliance, and enhancing comfort. The ability to access the skin subcaste enhances the effectiveness of invasomes, which exert their effects by fluidizing the bilayer structure of stratum corneum (SC) lipids and disrupting lipid and intracellular protein interactions. These recently discovered vesicles are tailored for use in topical and transdermal drug delivery due to their saturation effect and high deformability, distinguishing them from transferosomes.
Invasomes:用于透皮给药的囊状载体
透皮途径是局部或全身给药的重要途径。鉴于皮肤作为重要器官的重要性,开发通过这一途径给药的有效策略势在必行。Invasomes 是一种新型的囊泡系统,与传统的脂质体相比,它具有更强的透皮渗透性。内陷体由磷脂、乙醇和萜烯组成,具有适合软囊泡的透皮渗透特性。这些纳米囊泡提高了药物在表皮的渗透性,同时最大限度地减少了全身吸收,从而将药物作用限制在皮肤下层。与脂质体和乙硫体相比,入侵体能更深地渗透到皮肤中。它们具有多种优势,包括提高药物疗效、改善患者依从性和提高舒适度。侵入体通过使角质层(SC)脂质的双层结构流体化,破坏脂质与细胞内蛋白质的相互作用,从而发挥药效。这些最新发现的囊泡具有饱和效应和高变形性,有别于转移体,可用于局部和透皮给药。
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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