Preparation, characterization, and in vivo anti-ulcer evaluation of pantoprazole-loaded microparticles

被引:45
作者
Raffin, R. P.
Colome, L. M.
Pohlmann, A. R.
Guterres, S. S.
机构
[1] Univ Fed Rio Grande do Sul, Fac Farm, Program Posgrad Ciencias Farmaceut, BR-90610000 Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande Do Sul, Inst Quim, Dept Quim Organ, Porto Alegre, RS, Brazil
关键词
microparticles; pantoprazole; emulsification/solvent evaporation; polymer; gastric resistance; tablet; release profile; in vivo ulcer evaluation;
D O I
10.1016/j.ejpb.2006.01.013
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Pantoprazole is an important drug in the treatment of acid-related disorders. This work concerns the preparation and characterization of gastro-resistant pantoprazole-loaded microparticles prepared using an O/O emulsification/solvent evaporation technique. The in vivo activity of the pantoprazole-loaded Eudragit (R) S100 microparticles was carried out in rats. Furthermore, tablets containing the microparticles were also investigated. Microparticles presented spherical and smooth morphologies (SEM) and they remained intact in the inner surface of tablets. DSC and IR analyses showed that pantoprazole was physically and molecularly dispersed in the polymer. In vivo anti-ulcer evaluation showed that the microparticles were able to protect rat stomachs against ulcer formation, while the drug aqueous solution did not present activity. Drug dissolution profiles from tablets demonstrated slower release than untabletted microparticles. Weibull equation was the best model for describing the drug release profiles from microparticles and tablets. As regards the acid protection, tablets showed a satisfactory drug protection in acid medium (61.05 +/- 8.09% after 30 min). (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:198 / 204
页数:7
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