Formulation and evaluation of aceclofenac fast disintegrating tablets using sida acuta powder

T. Anjali, P. Prasanna Kumar, N. Srinivas, K. Shivaji
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Abstract

Aceclofenac is a NSAID with anti-inflammatory, analgesic activity. The aim is to develop the Aceclofenac tablets with sida acuta powder that exhibit rapid disintegration, dissolution and showing maximum pharmacological activity in less time. This is desirable for improving patient compliance. The present study was to formulate and evaluate the fast-disintegrating tablets of Aceclofenac using Sida acuta powder by direct compression technique with varying concentrations. Each formulation was evaluated for pre and post evaluation tests such as Flow property, Bulk density, tapped density, Weight variation, Hardness, Friability, Wetting time, Disintegration time, Assay, in-vitro dissolution. Among the 06 formulations, F6 formulation Aceclofenac with 6%w/w of Sida acuta showed the in-vitro dissolution (99.75%) release of drug within 20 minutes and release of drug mechanism as first order kinetics. It was concluded that the fast-disintegrating tablets are prepared by Natural polymer Sida acuta acts as a disintegrant and showed excellent disintegration time,enhance the dissolution rate.
使用西达拉粉配制和评估醋氯芬酸快速崩解片
醋氯芬酸是一种非甾体抗炎药,具有消炎和镇痛活性。开发醋氯芬酸片剂的目的是在西达乌头粉末中加入醋氯芬酸,使其在更短的时间内快速崩解、溶解并显示出最大的药理活性。这对于提高患者的依从性是非常理想的。本研究采用直接压片技术,使用西达乌头粉末配制并评估不同浓度的醋氯芬酸快速崩解片。每个配方都进行了前后评估测试,如流动性、堆积密度、压片密度、重量变化、硬度、易碎性、润湿时间、崩解时间、化验、体外溶解度。在 06 种配方中,F6 配方醋氯芬酸与 6%w/w 的西达乌头在 20 分钟内的体外溶解度(99.75%)和药物释放机理为一阶动力学。由此得出结论,天然聚合物西达乌头作为崩解剂制备的快速崩解片显示出极佳的崩解时间,提高了药物的溶解速率。
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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