...
首页> 外文期刊>Der Pharmacia Lettre >Formulation and Evaluation of Hydralazine Hydrochloride Orodisperdible Tablets By Direct Compression Method in the Treatment of Eclampsia And Pre-Eclampsia
【24h】

Formulation and Evaluation of Hydralazine Hydrochloride Orodisperdible Tablets By Direct Compression Method in the Treatment of Eclampsia And Pre-Eclampsia

机译:直接压片法制备盐酸肼屈嗪口腔分散片的研制及评价

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Introduction: Orodispersible tablets had received ever-increasing demand during the last decade, and the field has become a rapidly growing area in the pharmaceutical industry as oral drug delivery remains the preferred route for administration of various drugs. The purpose of the present research work was to formulate the orodispersible tablets of Hydralazine hydrochloride a drug of choice for eclampsia and pre-eclampsia to provide a suitable patient convenience dosage form an enhance to the bioavailability and to provide quick onset of action. Materials and Methods: Formulation of the orodispersible tablets of Hydralazine hydrochloride were prepared by using various superdisintegrants like crosspovidone, crosscarmellose sodium ,sodium starch glycolate by direct compression method. The formulas were evaluated for compatibility and Pre-Compression studies. The formulations were evaluated for weight variation, thickness, hardness, friability, content uniformity, disintegration time, wetting time, and water absorption ratio and release profile. Optimised formula was subjected to stability studies Results: Among all the formulations, F9 showed effective percentage of drug release at 12 minutes indicating faster and maximum absorption at the site of administration and showed superior quality based on stability reports.
机译:简介:在过去的十年中,油分散性片剂的需求量不断增加,并且该领域已成为制药行业快速发展的领域,因为口服药物递送仍然是各种药物给药的首选途径。本研究工作的目的是配制盐酸Hydralazine的口服分散片,作为先兆子痫和先兆子痫的一种选择药物,以提供合适的患者方便剂型,以增强生物利用度并提供快速起效的作用。材料与方法:盐酸肼屈嗪的口腔分散片的制备方法是使用多种超级崩解剂,如交叉聚维酮,交叉羧甲基纤维素钠,羟乙酸淀粉钠,通过直接压片法制备。评价配方的相容性和预压缩研究。评价制剂的重量变化,厚度,硬度,脆性,含量均匀性,崩解时间,润湿时间以及吸水率和释放曲线。对优化的配方进行了稳定性研究。结果:在所有配方中,F9在12分钟时显示出有效的药物释放百分比,表明在给药部位吸收更快,最大,并且根据稳定性报告显示出优异的质量。

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