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首页> 外文期刊>Indian drugs >FORMULATION AND EVALUATION OF MOUTH DISSOLVING TABLETS OF RANITIDINE HYDROCHLORIDE
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FORMULATION AND EVALUATION OF MOUTH DISSOLVING TABLETS OF RANITIDINE HYDROCHLORIDE

机译:盐酸拉尼替丁的可溶于口腔的片剂的制备和评价

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摘要

In present research work, taste masked Mouth Dissolving Tablets (MDTs) of Ranitidine Hydrochloride were designed with a view to enhance the patient compliance and provide a quick onset of action. Taste masking of the drug was done by formation of complex with [3 cyclodextrin. Tablets were prepared by direct compression, using superdisintegrants like crosscarmellose sodium and crosspovidone in different proportion and evaluated for the pre-compression parameters such as bulk density, compressibility, angle of repose etc. In view of the better taste palatability of such a bitter API, taste masking was carried out via making the cyclodextrin complex and sucralose was used as the sweetener to impart a palatable taste to the formulation. The prepared batches of tablets were evaluated for hardness, weight variation, friability, drug content, disintegration time and in vitro dissolution profile and found satisfactory. Among all, the formulation F7 containing 5% w/w proportion of both crosscarmellose sodium and crosspovidone was considered to be best formulation, which disintegrated completely in 19 seconds and released up to 98.38% of the drug.
机译:在当前的研究工作中,设计了雷尼替丁盐酸盐掩味口溶片(MDT),以增强患者的依从性并提供快速起效的作用。通过与[3-环糊精形成复合物来掩盖药物的味道。通过直接压片制备片剂,使用不同比例的交叉崩解纤维素钠和交叉聚维酮等超级崩解剂,并评估其预压制参数,例如堆积密度,可压缩性,休止角等。鉴于这种苦味API的口感更好,通过制备环糊精复合物来掩味,并且三氯蔗糖被用作甜味剂以赋予制剂可口的味道。对所制备的片剂批次进行硬度,重量变化,易碎性,药物含量,崩解时间和体外溶出曲线的评估,发现令人满意。在所有配方中,含有5%(w / w)交联羧甲基纤维素钠和交联聚维酮的配方F7被认为是最好的配方,它在19秒内完全崩解并释放出高达98.38%的药物。

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