期刊文献+

法莫替丁生物黏附片的处方筛选研究 被引量:4

Optimizing the Formulation of Famotidine Bioadhesive Tablets
下载PDF
导出
摘要 目的:筛选和优化法莫替丁生物黏附片的处方。方法:采用3因素9水平的均匀设计,结合多元线性回归的方法,以溶出度为指标,对制剂处方进行筛选、优化。结果:多元线性回归结果表明,处方中生物黏附材料HPMC、卡波姆对药物释放起阻滞作用,方程较好地阐明了主要辅料对法莫替丁生物黏附片释放度的影响。结论:均匀设计优化法莫替丁生物黏附片处方结果良好,优化处方的释放速度达到设计要求。 Objective:To screen and optimize the formulation of famotidine bioadhesive tablets(FBTs). Methods:A three- factor and ninelevel uniform design with multi- line-regression was performed to screen formulation of FBTs. The releasing behaviors of FBTs were evaluated by release test in vitro. Results:The results of regression showed that the amount of HPMC and carbomer was the main factor influencing drug release in vitro. The measuring cumulative release of FBTs fitted well the predictive cumulative release from the equation. Conclusion: It was effective and convenient to optimize the formulation of FBTs by uniform design and the drug release rate of FBTs reached the design requirements.
出处 《中国药业》 CAS 2005年第8期52-53,共2页 China Pharmaceuticals
关键词 法莫替丁 生物黏附片 均匀设计 处方筛选 famotidine bioadhesive tablet uniform design formulation screening
  • 相关文献

参考文献5

  • 1陈静,屠锡德.生物粘附性给药系统的研究[J].药学进展,2000,24(2):65-68. 被引量:17
  • 2李瑞雪.均匀设计在药物开发研究中的应用[M].成都:四川科学技术出版社,2000.27.
  • 3Smart JD, Kellaway 1W. Pharmaceutical factors influencing the rate of gas-trointestinal transit in an animal model [J]. lnt J Pharm, 1989,53 ( 1 ) ; 79.
  • 4Ohno H ,Sakai T,Tsuchida E ,et al. Interaction of human erythrocyte ghost or liposomes with polyethylene glyco detected by fluorescence polarization[J ].Biochem Biophys Rescommun, 1981,102( 1 ) :256.
  • 5Akiyama Y, Nagahara N, Nara E, et al. Evaluation of oral mucoadhesive microspheres in man on the basis of the pharmacokinetics of furosemide and riboflavin, compounds with limited gastrointestinal absorption sites [J].J Pharm Pharmcol, 1998,50 (2) : 159.

二级参考文献3

共引文献16

同被引文献47

  • 1刘国勤,吕玉麟,石建明,陈铁楼,马晓蓬,刘筠,侯惠民,贺芬.醋酸地塞米松粘贴片的研制[J].海军医学杂志,2000,21(2):138-139. 被引量:12
  • 2吴祥根,斯陆勤,李高.Thiomers/GSH体系——新型多肽类药物吸收促进剂[J].中国药学杂志,2005,40(5):328-330. 被引量:1
  • 3唐星,王成伟.常用生物黏附性高分子材料物理性质的比较试验[J].中国药学杂志,2005,40(5):361-364. 被引量:12
  • 4郭咸希,何文,罗云.N-三甲基壳聚糖对硝苯地平片在犬体内药物动力学的影响[J].中国药师,2007,10(2):103-105. 被引量:4
  • 5GERAGHTY P B, ATTWOOD D, COLLET J H, et al. An investigation of tile parameters influencing the bioadhesive properties of Myverol 18-99/water gels [ J ]. Bionmater, 1997,18 : 63 - 69.
  • 6GLANTZ P O, AMEBANT T, NYLANDER T, et al. Bioadhesive a phenomenon with multiple dimensions [ J]. Acta Odontol Scand, 1999,57 (5) :238 - 242.
  • 7GUPTA P, VERMANI K, GARG S. Hydrogels: from controlled realse to pH-responsive drug delivery [ J ]. Drug Discov Today,2002, 69(3) :379 -388.
  • 8BERTRAM U, BODMEIER R. In situ gelling, bioadhesive nasal inserts for extended drug delivery: in vitro characterization of a new nasal dosage form [ J ]. Eur J Pharm Sci,2006,27 ( 1 ) :62 - 71.
  • 9AHUJA A, KHAR R K. Mucoadhesiv drug delivery system [ J ]. Drug Dev lnd Pharm, 1998,23 ( 9 ) :489 - 515.
  • 10NOZAKI A, TOUCHAR D. Pharmaceutical and medical aspects of bioadhensive systems for drug administration [ J ]. Pharm Res, 1999, 16(40) :450 -457.

引证文献4

二级引证文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部