Development and Evaluation of Sucrose Free Herbal Orally Disintegrating Tablets of Ginger

Achhra Cv, P.T.N. Ha
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引用次数: 1

Abstract

The objective of the present study was to develop orally disintegrating tablets of dry ginger powder with sugar free ingredients. In the present research work, orally disintegrating tablets of ginger were prepared by wet granulation method. A total of eight formulations were prepared with different compositions. The formulated tablets were evaluated for post-compression parameters. FTIR spectroscopic studies revealed that there was no interaction between the dry ginger powder and other excipients used in the formulations. The disintegration time of the optimized formulation was less than 30 sec. The in vitro release study of optimized formulation showed more than 90% drug release at the end of 10 min. The optimized formulation B8 showed good in vitro and in vivo antimicrobial activity against Gram positive bacteria Staphylococcus aureus, Corynebacterium diphtheriae, Streptococcus pyogenes and Gram-negative bacteria Klebsiella pneumoniae. The formulation B8 was found to be stable for one month under accelerated stability condition.
无糖生姜口腔崩解片的研制与评价
本研究的目的是研制无糖干姜粉口腔崩解片。本研究采用湿造粒法制备生姜口腔崩解片。共制备了8种不同组成的复方。对配制的片剂进行压缩后参数评价。FTIR光谱研究表明,干姜粉与配方中使用的其他辅料之间没有相互作用。优化后的处方崩解时间小于30秒,体外释药试验结果表明,10 min时释药量大于90%。优化后的处方B8对革兰氏阳性菌金黄色葡萄球菌、白白链杆菌、化脓性链球菌和革兰氏阴性菌肺炎克雷伯菌均有良好的体外和体内抑菌活性。在加速稳定条件下,B8的稳定性为1个月。
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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