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Analysis of leukaemic cells dynamics with multi-stage maturation process using a new non-linear positive model with distributed time-delay

机译:使用具有分布时滞的新型非线性正模型,对白血病细胞进行多阶段成熟过程动力学分析

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摘要

This study proposes a new non-linear positive model with distributed time-delay describing the dynamics of leukaemic cells lineages and their levels of maturity. The dynamic model is first reformulated into coupled non-linear equations with distributed time-delay using an appropriate transformation of the age-structured transport partial differential equations that govern the dynamics of leukaemic cell populations. After assessing the positiveness of the proposed model, the conditions for the existence of positive steady-states are established. Furthermore, the necessary and sufficient conditions for boundedness of the solutions are derived. Finally, the convergence of the proposed model to the origin is studied as this has an important biological interpretation which is the extinction of all generations of leukaemic cells following anti-leukaemia treatments. To investigate the global asymptotic stability of this important equilibrium point, both model properties (i.e. positiveness and boundedness) are used to construct a suitable Lyapunov function for the characterisation of leukaemic cells dynamics. The results demonstrate a significant improvement for the treatment of leukaemia. Some simulations are presented to illustrate the effectiveness of the proposed model.
机译:这项研究提出了一个具有分布时间延迟的新型非线性正模型,该模型描述了白血病细胞谱系的动力学及其成熟水平。首先,通过对年龄结构的运输偏微分方程进行适当的变换,将动力学模型重新构建为具有分布式时延的耦合非线性方程,该方程控制白血病细胞群体的动力学。在评估了所提出模型的正性之后,确定了存在正稳态的条件。此外,得出了解的有界性的充要条件。最后,由于该模型具有重要的生物学解释,是抗白血病治疗后所有世代白血病细胞的灭绝,因此研究了该模型与原点的融合。为了研究这一重要平衡点的全局渐近稳定性,两种模型特性(即正性和有界性)都用于构建合适的Lyapunov函数,用于表征白血病细胞动力学。结果证明了白血病治疗的显着改善。提出了一些仿真来说明所提出模型的有效性。

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