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On Analysis of Parameter Estimation Model for the Treatment of Pathogen-Induced HIV Infectivity

机译:关于治疗病原菌感染HIV的参数估计模型的分析

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Multiplicity of new cases of HIV/AIDS and its allied infectious diseases daunted by lack of proper parametric estimation necessitated this present work. Formulated using ordinary differential equation was a five-dimensional (5D) differential mathematical model with which compatibility of optimal control strategy for dual (viral load and parasitoid-pathogen) infectivity in the blood plasma was investigated. Discretization method indicated the incompatibility of the model due to large error derivatives. The study using numerical method established treatment set point with which we explored the variation of predominant model parameters and thereof investigated the maximization of uninfected healthy CD4 ) T cell count as well as the de-replication of viruses following the consistent administration of reverse transcriptase inhibitor from set point. Presented was a series of numerical calculations obtained using well-known Runge-Kutter of order of precision 4, in Mathcad platform. Analysis of simulated parameters showed that distortion of replication viruses and de-transmutation of susceptible CD4 ) T cells by viruses via chemotherapy led to restoration and gradual increase of healthy blood plasma, with near zero declination of both viral load and parasitoid-pathogen within chemotherapy validity time frame. The model was worthy in the study of treatment analysis of dual HIV—pathogen infection and thereof recommended for other related dual infectious diseases.
机译:由于缺乏适当的参数估计而令人生畏的新的艾滋病毒/艾滋病及其相关传染病病例众多,因此需要开展这项工作。使用普通的微分方程式建立了一个五维(5D)微分数学模型,该模型研究了血浆中双重(病毒载量和寄生虫病原体)传染性的最佳控制策略的兼容性。离散化方法表明模型存在较大的误差导数,因此不兼容。使用数值方法进行的研究建立了治疗设定点,通过该设定点我们探索了主要模型参数的变化,并研究了未感染的健康CD4 + T细胞计数的最大化以及在持续施用来自的逆转录酶抑制剂后病毒的复制设定点。在Mathcad平台上,展示了使用精度为4的著名Runge-Kutter获得的一系列数值计算。对模拟参数的分析表明,复制病毒的变形和病毒通过化学疗法使易感CD4 + T细胞脱变导致健康血浆的恢复和逐渐增加,在化学疗法有效期内病毒载量和寄生虫病原体的偏斜几乎为零大体时间。该模型值得用于HIV双重感染-病原体感染的治疗分析研究,并推荐用于其他相关的双重感染性疾病。

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