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首页> 外文期刊>Drug delivery and translational research >Neuro-fuzzy modeling of ibuprofen-sustained release from tablets based on different cellulose derivatives
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Neuro-fuzzy modeling of ibuprofen-sustained release from tablets based on different cellulose derivatives

机译:基于不同纤维素衍生物的片剂中布洛芬持续释放的神经模糊建模

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In the present study, we investigated the drug release behavior from cellulose derivative (CD) matrices in the oral form of tablets. We used the adaptive neural-fuzzy inference system (ANFIS) to predict the best formulation parameters to get the perfect sustained drug delivery using ibuprofen (IB) as a model drug. The different formulations were prepared with different CDs, namely CMC, HEC, HPC, HPMC, and MC. The amount of the active ingredient varied between 20 and 50%. The flow properties of the powder mixtures were evaluated for their angle of repose, compressibility index, and Hausner ratio, while the tablets were evaluated for weight uniformity, hardness, friability, drug content, disintegration time, and release ratio. All tablet formulations presented acceptable pharmacotechnical properties. In general, the results showed that the drug release rate increases with an increase in the loaded drug. Kinetic studies using the Korsmeyer-Peppas equation showed that different drug release mechanisms were involved in controlling the drug dissolution from tablets. The drug release mechanism was influenced by the gel layer strength of the CDs formed in the dissolution medium. The mean dissolution time (MDT) was determined and the highest MDT value was obtained for the HPMC formulations. Moreover, HPMC exhibited release profiles adequate for sustained release formulations for over 14h. The intelligent model based on the experimental data was used to predict the effect of the polymer's nature, the amount of the active ingredient, and the kinetic release profile and rate (R-2=0.9999 and RMSE=5.7x10(-3)). The ANFIS model developed in this work could accurately model the relationship between IB release behavior and tablet formulation parameters. The proposed model was able to successfully describe this phenomenon and can be considered an efficient tool with predictive capabilities that is useful for the designing and testing of new dosage systems based on polymers.
机译:在本研究中,我们研究了在口服片剂中的纤维素衍生物(CD)基质中的药物释放行为。我们使用了自适应神经模糊推理系统(ANFIS)来预测最佳配方参数,以获得使用布洛芬(IB)作为模型药物的完美持续药物递送。用不同的Cds,即CMC,HEC,HPC,HPMC和MC制备不同的配方。活性成分的量在20%和50%之间变化。评价粉末混合物的流动性,用于它们的休息角,可压缩性指数和Hausner比,同时评估片剂的重量均匀性,硬度,脆性,药物含量,崩解时间和释放比。所有片剂配方均呈现可接受的药房性质。一般来说,结果表明,随着负载药物的增加,药物释放速率增加。使用Korsmeyer-Peppas方程的动力学研究表明,不同的药物释放机制涉及控制片剂的药物溶解。药物释放机制受溶解介质中形成的CD的凝胶层强度的影响。测定平均溶解时间(MDT)并获得最高的MDT值,用于HPMC制剂。此外,HPMC表现出足够的释放型材以持续释放制剂超过14小时。基于实验数据的智能模型用于预测聚合物性质,活性成分的量和动力学释放曲线的影响和速率(R-2 = 0.9999和RMSE = 5.7×10(-3))。在这项工作中开发的ANFI模型可以准确地模拟IB发布行为和平板电脑配方参数之间的关系。所提出的模型能够成功描述这种现象,可以被认为是一种有效的工具,具有可用于基于聚合物的新剂量系统的设计和测试。

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