Formulation and Evaluation of Orodispersible Tablet of Sulindac

Bhavna B. Gaikwad, B. Rane, Ashish Jain
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引用次数: 1

Abstract

Oral administration of dosage form is the most recommended mode of administration, because of its self-medication, accurate dose of the drug, and ease of administration. However, trouble swallowing in geriatric patients is one major negative of this route, which can mentally disrupt patients. The goal of this study was to use the direct compression method to make orodispersible tablets of sulindac utilizing various doses of super disintegrant agents such as Sodium starch glycolate Crospovidone and Croscarmellose sodium. Three distinct super disintegrants were used to create nine formulations with varying concentration levels. The preformulation, precompression, and post-compression properties of the powder combinations were assessed. In comparison to the other formulations, tablets from batch F3 containing crospovidone had superior organoleptic qualities, as well as outstanding drug release and in-vitro disintegration time. The super disntegrants addition technique was shown to be a viable method for manufacturing orodispersible tablets using the direct compression method.
舒林达多孔分散片的研制及评价
口服给药是最推荐的给药方式,因为它可以自行给药,剂量准确,给药方便。然而,老年患者的吞咽困难是这条路线的一个主要负面影响,它可能会扰乱患者的精神。本研究的目的是利用不同剂量的高崩解剂如淀粉乙醇酸钠、交联维酮和交联纤维素钠,采用直接加压法制备舒林酸非分散片。三种不同的超级崩解剂被用来制造9种不同浓度水平的配方。评估了粉末组合的配方前、压缩前和压缩后的性能。与其他制剂相比,F3批含交叉维酮片具有较好的感官品质,且具有较好的药物释放和体外崩解时间。超级分散剂的加入技术是一种可行的直接压缩法制备非分散片剂的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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