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METHOD TO IDENTIFY LIVER TOXICITY USING METABOLITE PROFILES

机译:代谢物特征鉴定肝脏毒性的方法

摘要

The present disclosure relates to a methodology that identifies the underlying mechanisms that lead to hepatotoxicity. This is done by using the alterations in cellular metabolite profiles obtained before and after therapy/drug treatment in combination with a model of liver metabolism. Subsequently, by using a covariance matrix adaptation followed by evolutionary selection, it compares the drug-induced metabolite profiles obtained experimentally with those generated using the in silico model, automatically shortlists potential parameters whose alterations could have produced the drug-treated metabolite profile. Values of these parameters are estimated by formulating an optimal control problem to minimize the differences between the model-generated metabolite values and experimentally observed data. The estimated parameters are given as an input to the homeostatic liver model and simulations are carried out, thereby the results providing a mechanistic explanation for the development of toxicity.
机译:本公开涉及鉴定导致肝毒性的潜在机制的方法。这是通过将治疗/药物治疗之前和之后获得的细胞代谢物谱变化与肝脏代谢模型结合起来完成的。随后,通过使用协方差矩阵适应和随后的进化选择,将实验获得的药物诱导的代谢产物谱与使用计算机模型生成的代谢产物谱进行比较,自动列出其参数可能会产生药物处理的代谢产物谱的潜在参数。通过制定最佳控制问题以最小化模型生成的代谢物值与实验观察到的数据之间的差异,可以估算这些参数的值。给出估计的参数作为稳态肝模型的输入,并进行模拟,从而为毒性的产生提供机理解释。

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