瑞格列奈基质透皮治疗系统的设计与评价

M. Sahu, M. Bhowmick, J. Rathi
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摘要

http://dx.doi.org/10.21276/IJRDPL.227 8-0238.2017.6(4)。摘要:本研究旨在开发一种基质型透皮系统,该系统能够将选定的降糖药瑞格列奈以所需的治疗浓度长期递送。透皮给药系统的原理是通过表皮传递药物,在较长时间内达到全身效果。由于这些特性,经皮给药系统提供了许多优点,如减少副作用,提高患者依从性,消除首过代谢和持续给药。抗糖尿病药物,对治疗高血糖疾病很重要。这类抗糖尿病药物是快速的,口服后几乎完全从胃肠道吸收,但经历广泛的首过代谢。因此,单次口服后血药浓度峰值迅速出现,生物利用度为56%,正常受试者半衰期为1小时。因此,需要设计一种药物传递系统,使降糖药瑞格列奈能够以可控的方式长时间传递,以避免药物相关的副作用。考虑到口服降糖药瑞格列奈存在的这些问题,我们尝试开发经皮给药系统,以获得更好的释放模式。作者:MithileshSahu, NRI Pharmaceutical Sciences Institute, Bhopal, Madhya Pradesh, India。E-mail address: mithun211@gmail.com
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Design and evaluation of Matrix Transdermal therapeutic system of Repaglinide
http://dx.doi.org/10.21276/IJRDPL.227 8-0238.2017.6(4).2697-2705 ABSTRACT:The present study is an attempt to develop a Matrix type transdermal system capable of delivering the selected antidiabetic drug Repaglinide in the desired therapeutic concentration for prolong period. The principle of transdermal drug delivery systems is to deliver drug across epidermis to achieve systemic effect over a prolonged period of time. Because of these attributes, transdermal drug delivery systems offer many advantages such as reduced side effects, improved patient compliance, elimination of first-pass metabolism, and sustained drug delivery. Antidiabetic drug which is important for the treatment of hyperglycemic disorders. This category of anti-diabetic drugs is rapid and almost completely absorbed from the GIT following oral administration, but undergoes extensive first pass metabolism. Therefore, the peak plasma concentration occurs rapidly and after a single oral dose and bioavailability is 56%, the half-life of elimination is 1 hour in normal subject. Hence, it is required to design a drug delivery system which may deliver antidiabetic drug Repaglinide in controlled manner for a prolonged period to circumvent the drug related side effects. Considering all these problems associated with oral administration of anti-diabetic drug Repaglinide, attempt has been made to develop transdermal drug delivery system in order to achieve a better release pattern. ⇑ Corresponding author at: MithileshSahu, NRI Institute of Pharmaceutical Sciences, Bhopal, Madhya Pradesh, India E-mail address: mithun211@gmail.com INTRODUCTION
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