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首页> 外文期刊>FEBS Letters >Efficient and cost‐effective experimental determination of kinetic constants and data: the success of a Bayesian systematic approach to drug transport, receptor binding, continuous culture and cell transport kinetics
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Efficient and cost‐effective experimental determination of kinetic constants and data: the success of a Bayesian systematic approach to drug transport, receptor binding, continuous culture and cell transport kinetics

机译:高效,经济高效地确定动力学常数和数据的实验方法:贝叶斯系统方法在药物转运,受体结合,连续培养和细胞转运动力学方面的成功

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摘要

>Details about the parameters of kinetic systems are crucial for progress in both medical and industrial research, including drug development, clinical diagnosis and biotechnology applications. Such details must be collected by a series of kinetic experiments and investigations. The correct design of the experiment is essential to collecting data suitable for analysis, modelling and deriving the correct information. We have developed a systematic and iterative Bayesian method and sets of rules for the design of enzyme kinetic experiments. Our method selects the optimum design to collect data suitable for accurate modelling and analysis and minimises the error in the parameters estimated. The rules select features of the design such as the substrate range and the number of measurements. We show here that this method can be directly applied to the study of other important kinetic systems, including drug transport, receptor binding, microbial culture and cell transport kinetics. It is possible to reduce the errors in the estimated parameters and, most importantly, increase the efficiency and cost-effectiveness by reducing the necessary amount of experiments and data points measured.
机译:>动力学系统参数的详细信息对于医学和工业研究(包括药物开发,临床诊断和生物技术应用)的进展至关重要。这些细节必须通过一系列动力学实验和研究来收集。实验的正确设计对于收集适用于分析,建模和得出正确信息的数据至关重要。我们已经开发出系统的迭代贝叶斯方法和酶动力学实验设计的规则集。我们的方法选择最佳设计来收集适合于精确建模和分析的数据,并最大程度地减少估计参数的误差。该规则选择设计的特征,例如基材范围和测量次数。我们在这里表明,该方法可以直接应用于其他重要的动力学系统的研究,包括药物转运,受体结合,微生物培养和细胞转运动力学。可以减少估计参数的误差,最重要的是,通过减少必要的实验和测得的数据点数量,可以提高效率和成本效益。

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