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A method to determine pharmacokinetic parameters based on andante constant-rate intravenous infusion
On account of the disturbance from the distribution phase, the concentration-time curve of drugs cannot fully reflect the characteristics of elimination, and thus, it is difficult for present methods to obtain ideal pharmacokinetic parameters. This paper presents a method to determine pharmacokineti...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5643313/ https://www.ncbi.nlm.nih.gov/pubmed/29038495 http://dx.doi.org/10.1038/s41598-017-13437-6 |
Sumario: | On account of the disturbance from the distribution phase, the concentration-time curve of drugs cannot fully reflect the characteristics of elimination, and thus, it is difficult for present methods to obtain ideal pharmacokinetic parameters. This paper presents a method to determine pharmacokinetic parameters based on an andante constant-rate intravenous infusion. A mathematical model of the constant-rate intravenous infusion combined with the elimination of first-order kinetics was established. During infusion, the accumulation tendency of drugs was deduced as [Formula: see text] using the principle of calculus. Then, the method to determine the pharmacokinetic parameters was summed up. After collecting the blood drug concentration (C (t)) -time (t) data from a constant-rate (v) infusion period, an exponential regression analysis was conducted to obtain the elimination rate constant (K) and plateau concentration (C (ss)). Then, the half-life (t (1/2)), apparent volume of distribution (V (d)) and clearance rate (CL) were calculated based on the equations, t (1/2) = 0.693/K, V (d) = (v/K)/C (ss) and CL = v/C (ss), respectively. In addition, an application example of cimetidine in a beagle dog was used to demonstrate the implementation process of the method. |
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