...
首页> 外文期刊>International Journal of Pharmaceutical Sciences and Research >FAST DISSOLVING TABLETS OF FEXOFENADINE HYDROCHLORIDE BY MELT TECHNOLOGY: FORMULATION AND CHARACTERIZATION
【24h】

FAST DISSOLVING TABLETS OF FEXOFENADINE HYDROCHLORIDE BY MELT TECHNOLOGY: FORMULATION AND CHARACTERIZATION

机译:熔融制盐酸非索非那定片的快速溶解片剂:制剂和表征

获取原文

摘要

The objective of present study was formulation and evaluation of fast release tablets of Fexofenadine hydrochloride. Fexofenadine hydrochloride is an anti-histamine with selective H1-receptor antagonist activity. In this investigation fast release tablets of Fexofenadine hydrochloride were prepared using cross povidone as a superdisintegrants by melt technology method. The Fourier transform infrared spectroscopy revealed absence of any drug – excipient interactions. The tablets were evaluated for pre-compressed evaluation like bulk density, tapped density, Hauser’s ratio, Carr’s index and angle of repose and post-compressed evaluation like weight variation, thickness, hardness, friability, wetting time, disintegration time, content uniformity and in-vitro drug release profile. The wetting time for all batches was found in the range of 20.1 to 80.1 sec. All the tablets were disintegrated within 100 seconds. In-vitro percent drug release was found up to 98.25 % in 30 min. The formulation 4 showed better result in wetting time, disintegration time and drug release profile.
机译:本研究的目的是配制和评价盐酸非索非那定的速释片。盐酸非索非那定是具有选择性H 1 -受体拮抗剂活性的抗组胺药。在这项研究中,通过交叉聚维酮作为超级崩解剂,通过熔融技术方法制备了盐酸非索非那定的速释片剂。傅立叶变换红外光谱显示不存在任何药物-赋形剂相互作用。对片剂进行压缩前评估,如堆积密度,堆积密度,豪瑟比,卡尔指数和休止角;压缩后评估如重量变化,厚度,硬度,脆性,润湿时间,崩解时间,含量均匀性和-体外药物释放曲线。发现所有批次的润湿时间为20.1至80.1秒。所有片剂在100秒内崩解。在30分钟内发现体外药物释放百分比高达98.25%。制剂4在润湿时间,崩解时间和药物释放曲线方面显示出更好的结果。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号