帕洛诺司琼透皮贴剂止吐的体外评价

Atul Tripathi, P. Tyagi, A. Vyas, Beena Gidwani, Amol Chandekar, H. Sharma
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引用次数: 3

摘要

皮肤是通过各种给药系统给药的途径之一。透皮给药系统(TDDS)是一种最可靠、最实用的通过皮肤给药系统。一般来说,药物贴片是贴在皮肤上,通过它将药物输送到血液中。本研究的目的是研制并评价帕洛诺司琼体外透皮贴剂用于止吐的效果。帕洛诺司琼是一种5-羟色胺5-羟色胺3拮抗剂。采用溶剂蒸发法制备TDDS,并对TDDS的感官特性和其他理化性能进行了评价,包括厚度、重量变化、药物含量均匀性、拉伸强度、伸长率、折叠耐久性和水分含量。采用KesaryChein扩散细胞作为屏障膜,对该贴片进行体外透性研究。以pH 7.4的磷酸盐缓冲液作为溶出介质,温度保持在37±10℃。所制备贴片的体外渗透研究表明,在整个研究过程中,药物释放呈时间依赖性增加。24 h内累积释药率为76.25%。这项研究显示了一种与帕洛诺司琼一起工作的新方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vitro evaluation of Transdermal Patch of Palonosetron for Antiemetic Therapy
Skin is one of the routes for systemic delivery of drugs through various drug delivery system. A transdermal Drug Delivery System (TDDS) is one of the most reliable and useful system to deliver drug systemically through skin. Generally medicated patch is placed on skin for delivery of medication through it into the blood stream. The aim of present study was to formulate and evaluate Palonosetron transdermal patch in vitro that could be used for antiemetic therapy. The incorporation ofPalonosetron a serotonin 5-HT 3 antagonist drug was envisaged. The TDDS was prepared by solvent evaporation technique and was evaluated for organoleptic characteristics and other physicochemical properties Thickness, Weight variation, Drug content uniformity, Tensile strength, % Elongation, Folding endurance & Moisture content. The in vitro permeation study of the patch was carried out through KesaryChein diffusion cell as barrier membrane. Phosphate buffer pH 7.4 was used as dissolution medium and the temperature was maintained at 37 ± 1 0 C. The in vitro permeation study of the prepared patch indicated a time dependent increase in drug release throughout the study. The percentage of cumulative drug release was found to be 76.25% in 24 hours.The study shows a new approach to work in with Palonosetron.
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