Formulation and Evaluation of Rapimelt Tablet of Anti-Vertigo Drug (Lorazepam)

B. M. Kadu, S. Bhasme, R. D. Bawankar, D. Mundhada
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Abstract

A. Rapimelt tablet of Lorazepam was prepared by direct compression method using Indion 414, Cross Carmellose Sodium and sodium starch glycolate as superdisintegrants with aim to get rapid onset of action, improve bioavailability and to give pleasant taste and better mouth feel. The tablets prepared were evaluated for various parameters like various density parameters, thickness, hardness, friability, disintegration time, wetting time and invitro dissolution time and were found to be within limits as per Indian Pharmacopoeia. FT-IR spectra of physical mixture of Lorazepam with Indion 414showedretention of basic peaks of Lorazepam. The developed formulation of Lorazepam batch F5 (10% Indion 414) showed good palatability and dispersed within 30 seconds as compared to Crosscarmellose Sodium batches F1-F3 and Sodium starch glycolate batches F6-F9.
抗眩晕药(劳拉西泮)拉吡美特片的研制及评价
A.采用直接加压法制备劳拉西泮拉皮美特片,以印度酮414、十字卡麦糖钠和乙醇酸淀粉钠为超崩解剂,目的是提高起效快、生物利用度、口感好。对制备的片剂进行了密度参数、厚度、硬度、脆性、崩解时间、润湿时间、体外溶出时间等参数的评价,均在印度药典规定的限度内。劳拉西泮与铟414物理混合物的红外光谱显示劳拉西泮的碱性峰保留。与交叉淀粉钠批次F1-F3和乙醇酸淀粉钠批次F6-F9相比,所研制的劳拉西泮批次F5(10%铟414)具有良好的食性和30秒内分散性能。
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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