首页> 外文期刊>Journal of Drug Delivery and Therapeutics >DESIGN AND IN-VITRO EVALUATION OF STOMACH SPECIFIC FLOATING MICROSPHERES OF OMEPRAZOL
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DESIGN AND IN-VITRO EVALUATION OF STOMACH SPECIFIC FLOATING MICROSPHERES OF OMEPRAZOL

机译:奥美唑气孔特定漂浮微球的设计和体外评价

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In this present study attempt was made to prepare the floating microspheres of Omeprazol which will help in releasing the proton pump inhibitor drugs in stomach. So that they can be absorbed in stomach for a longer period of time and show better bioavailability. The IR spectrum of pure drug and drug mixture indicated that there was no interaction between polymers and drug. The DSC also revealed that there was no interaction between polymers and drug. The shape of microspheres was almost spherical and smooth as indicated by SEM. Encapsulation efficiency was in the range of 66.23±0.115 to 88.53±0.578%. As the polymer concentration increases, the encapsulation efficiency also increases. In vitro buoyancy studies of the prepared microspheres was in the range of 70.9 to 79.1%.Omeprazol release from microspheres was slow and extended period of time due to increase in polymer concentration. The release mechanisms for all the formulation followed by non-fickian diffusion mechanism. The drug release from formulation OMP6 showed 87.26% for a long period of 12hrs and also observed that increase in Eudragit S100 concentration the drug release was decreased. The release mechanisms for all the formulation followed by non-fickian diffusion mechanism.
机译:在本研究中,尝试制备了奥美拉唑的漂浮微球,这将有助于在胃中释放质子泵抑制剂药物。这样它们就可以在胃中吸收更长的时间,并显示出更好的生物利用度。纯药物和药物混合物的红外光谱表明,聚合物和药物之间没有相互作用。 DSC还显示,聚合物与药物之间没有相互作用。如SEM所示,微球的形状几乎为球形且光滑。包封效率在66.23±0.115至88.53±0.578%的范围内。随着聚合物浓度的增加,包封效率也增加。制备的微球的体外浮力研究在70.9%至79.1%范围内。由于聚合物浓度的增加,奥美拉唑从微球中的释放缓慢且时间延长。所有制剂的释放机理均遵循非菲克扩散机理。从制剂OMP6释放的药物在12个小时的长时间内显示为87.26%,并且还观察到Eudragit S100浓度的增加使药物释放减少。所有制剂的释放机理均遵循非菲克扩散机理。

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