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Application of Gravitational Search Algorithm on the Modified Compartmental Absorption and Transit Model for Predicting Oral Drug Absorption

机译:重力搜索算法在修正隔室吸收和转运模型中预测口服药物吸收的应用

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The rate of oral drug absorption can be predicted using the compartmental absorption and transit (CAT) model. In this paper, the CAT model has been modified by combining the dissolution constant in seven compartments in the small intestine to define the plasma concentration of the oral drug, Atenolol. The simulations were performed using the MATLAB program and optimized by gravitational search algorithm (GSA) technique. Based on the results of the simulation the prediction of plasma concentration of Atenolol at doses of 25, 50, and 100 mg, the MCAT model with GSA optimization has a better prediction as compared to the MCAT simulation only. The determination coefficient values (R2) are increased from the range of 80% to more than 90% and show that the simulation results fit very well with the experimental data. The inclusion of GSA helps to optimize the MCAT model in predicting the plasma concentration of drug in the absorption, distribution, and metabolism phase (the first 8 hours after drug administration).
机译:口服药物吸收的速率可以使用隔室吸收和转运(CAT)模型进行预测。在本文中,通过组合小肠中七个小室中的溶出常数来定义口服药物阿替洛尔的血浆浓度,从而修改了CAT模型。仿真是使用MATLAB程序进行的,并通过重力搜索算法(GSA)技术进行了优化。根据模拟结果预测剂量为25、50和100 mg时阿替洛尔的血浆浓度,与仅进行MCAT模拟相比,具有GSA优化的MCAT模型具有更好的预测。测定系数值(R 2 )从80%的范围增加到90%以上,并且表明仿真结果与实验数据非常吻合。包含GSA有助于优化MCAT模型,以预测药物在吸收,分布和代谢阶段(给药后的前8小时)的血浆浓度。

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