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首页> 外文期刊>International Journal of Pharmaceutical Sciences and Research >DESIGN OF CONTROLLED RELEASE NON-ERODIBLE POLYMERIC ATENOLOL MATRIX TABLET USING MICROWAVE OVEN-ASSISTED SINTERING TECHNIQUE
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DESIGN OF CONTROLLED RELEASE NON-ERODIBLE POLYMERIC ATENOLOL MATRIX TABLET USING MICROWAVE OVEN-ASSISTED SINTERING TECHNIQUE

机译:使用微波炉辅助烧结技术设计控制释放不可侵蚀聚合物亚谷醇基片

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The objective of the present study was to evaluate the effect of microwave sintering condition on matrix formation and subsequent drug release from polymer matrix tablet for controlled release. The Atenolol floating SR matrix tablets were prepared by using tragacanth, sodium bicarbonate, Eudragit S-100 and citric acid was incorporated as a gas generating agents. Atenolol controlled release tablets were estimated in terms of their physico-chemical parameter like weight variation, friability, hardness, drug content, contact angle, floating lag time emin-vitro/em drug release, specific gravity and stability study as per ICH guidelines. The results of emin-vitro/em drug release studies showed that the optimized formulation (F6, L2, I2, H4) could extend drug release (99.5%) for 24 hours. The release pattern of Atenolol was fitted to different models based on coefficient of correlation (r). The present work also deals with the application of sintering technique to matrix tablets of Atenolol to achieve sustained release. The results of the present work stated that sintering caused decrease in drug release as compared to unsintered tablets. It was found that F6, L2, I2 and H$ gave better results compared to other formulations. The stability studies were carried out according to ICH guideline which indicates that the selected formulations were stable. Hence we finally conclude that microwave oven sintering is better than conventional hot air oven sintering process in preparation of controlled release tablets.
机译:本研究的目的是评估微波烧结条件对基质形成和随后从聚合物基质片剂进行控制释放的效果。通过使用TragaCanth,碳酸氢钠,Eudragit S-100和柠檬酸掺入作为气体发生剂来制备阿绿龙浮动SR基质片剂。估计阿替洛尔控释片剂的物理化学参数估计,如重量变异,脆性,硬度,药物含量,接触角,浮动滞后时间体外药物释放,比重和稳定性研究每条准则。 在体外药物释放研究结果表明,优化的制剂(F6,L2,I2,H4)可以延长药物释放(99.5%)24小时。基于相关系数(R),适用于不同模型的释放模式。目前的工作还涉及烧结技术在阿谷醇达到持续释放的基质片段中的应用。目前工作的结果表明,与未烧结的片剂相比,烧结引起的药物释放减少。发现与其他配方相比,F6,L2,I2和H $给出了更好的结果。根据ICH指南进行稳定性研究,表明所选配方稳定。因此,我们最终得出结论,微波炉烧结比传统的热空气烘箱烧结过程更好,用于制备控释片剂。

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