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Numerical solution of inverse problem for secretion and kinetics of C-peptide model

机译:C-肽模型分泌和动力学反问题的数值解

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The minimal model of insulin secretion based on C-peptide data (Toffolo et al., 1995) is presented in this report. The secretion model is identified on C-peptide taken in plasma; it must be integrated into a model of whole-body C-peptide kinetics. The kinetic model is the one proposed by (Eaton et al., 1980) and consists of 2 compartments. Compartment 1, accessible to measurement, represents plasma and rapidly equilibrating tissues, whereas compartment 2 represents tissues in slow exchange with plasma. This model allows estimating distribution of insulin in the blood and tissues. A new iterative algorithm for finding kinetic constants and secretion parameters is proposed. Numerical solution of inverse problem was obtained by using synthetic data. Different levels of noise were added to such data. The question of initial approximation is covered in this talk.)
机译:本报告中提出了基于C-肽数据的胰岛素分泌的最小模型(Toffolo等,1995)。分泌模型在血浆中取出的C肽上鉴定出来;它必须集成到全体C-肽动力学的模型中。动力学模型是(Eaton等,1980)所提出的模型,由2个隔间组成。隔室1可访问的测量,代表血浆和快速平衡的组织,而隔室2代表与等离子体缓慢交换中的组织。该模型允许估计血液和组织中胰岛素的分布。提出了一种用于找到动力学常数和分泌参数的新迭代算法。通过使用合成数据获得逆问题的数值解。在这些数据中添加了不同噪声水平。初始近似的问题是在此谈话中涵盖的。)

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