Literature DB >> 21050887

Floating matrix dosage form for dextromethorphan hydrobromide based on gas forming technique: in vitro and in vivo evaluation in healthy volunteers.

Liandong Hu1, Li Li, Xun Yang, Wei Liu, Jianxue Yang, Yanhong Jia, Chuang Shang, Hongxin Xu.   

Abstract

The objective of this study was to develop the dextromethorphan hydrobromide sustained-release (DMB-SR) tablets using floating technique to prolong the gastric residence time and compared their pharmacokinetic behavior with conventional sustained release tablets. DMB-SR floating tablets were prepared employing hydroxypropyl methylcellulose (HPMC) as hydrophilic gel material, sodium bicarbonate as gas-generating agent and hexadecanol as floating assistant agent. An orthogonal experiment design method was used to select the optimized formulation. The floating tablets were evaluated for uniformity of weight, hardness, friability, drug content, floating characteristics, in vitro release and in vivo bioavailability. The optimized tablets were prepared with HPMC K4M 25 mg, sodium bicarbonate 20 mg and hexadecanol 18 mg. The prepared tablets could float within 3 min and maintain for more than 24 h. The data of physical parameters were all lie within the limits. Drug release at 12 h was more than 85%. The comparative pharmacokinetic study was performed by administration of the DMB-SR floating tablets and conventional DMB-SR tablets. The area under curve of plasma concentration-time (AUC) of floating tablets was slightly higher than that of reference tablets, T(max) was prolonged apparently. The results showed the floating tablets are a feasible approach for the sustained-release preparation of drugs, which have limited absorption sites in the stomach.
Copyright © 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 21050887     DOI: 10.1016/j.ejps.2010.10.010

Source DB:  PubMed          Journal:  Eur J Pharm Sci        ISSN: 0928-0987            Impact factor:   4.384


  2 in total

1.  Matrix tablets: the effect of hydroxypropyl methylcellulose/anhydrous dibasic calcium phosphate ratio on the release rate of a water-soluble drug through the gastrointestinal tract I. In vitro tests.

Authors:  Pseidy L Mamani; Roberto Ruiz-Caro; María D Veiga
Journal:  AAPS PharmSciTech       Date:  2012-08-21       Impact factor: 3.246

2.  Preparation and in vitro-in vivo evaluation of acyclovir floating tablets.

Authors:  Rahim Bahri-Najafi; Abolfazl Mostafavi; Naser Tavakoli; Somayeh Taymouri; Mohammad-Mehdi Shahraki
Journal:  Res Pharm Sci       Date:  2017-04
  2 in total

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