转移体:用于增强药物渗透的囊性透皮给药系统的叙述综述

Syeda Jabeen Unnisa, Swarupa Arvapalli, B. Karunakar, PS Reddy, A. Vaishnavi, J. Sharma
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引用次数: 1

摘要

经皮给药一般受皮肤血管系统屏障功能的限制,是活性物质经皮给药方法中争议最大的方法之一。透皮给药系统是设计用于通过皮肤递送生物活性药物,主要是通过扩散产生局部内部作用,如果不是全身作用的话。在发现诸如转移体、醇体、立方体体、植物体等弹性囊泡后,经皮给药系统重新启动。转移体是一种弹性或可变形的囊泡,于20世纪90年代初被引入。弹性是通过在脂质双分子层结构中加入边缘活化剂而产生的。药物被吸收并分布到器官和组织中,并从体内排出,必须在不同的位置通过一个或多个生物膜,这种药物穿过膜的运动被称为药物运输,药物传递要穿过身体,它应该通过膜屏障。设计这种给药系统的概念是为了将药物的量集中在剩余的药物中;因此,以磷脂为基础的载体体系在这个时代引起了相当大的兴趣。
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A NARRATIVE REVIEW ON TRANSFERSOMES: VESICULAR TRANSDERMAL DELIVERY SYSTEM FOR ENHANCED DRUG PERMEATION
Transdermal administration of drug is generally limited by the barrier function of the skin vascular system are one of the most controversial method for transdermal delivery of active substance. transdermal drug delivery system is designed to deliver biological active agents through the skin, principally by diffusion for local internal if not systemic effects. The transdermal delivery system was relaunched after the discovery of elastic vesicles like transfersome, ethosome, cubosome, phytosome etc. Transfersomes are a form of elastic or deformable vesicle, which were introduced in the early 1990s. Elasticity is generated by incorporation of edge activator in lipid bilayer structure. Drug absorbed and distributed into organs and tissue and eliminated from the body it must pass through one or more biological membranes at various locations such movement of drug across the membrane is called as drug transport for the drug delivery to cross the body it should pass through the membrane barrier. This concept of drug delivery system was designed in attempt to concentrate the amount of drug in the remaining drug; therefore, the phospholipid-based carrier system is of considerable interest in the era.
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