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健康男性体内生物电阻抗与茶碱药代动力学参数的关系。

Relationship of bioelectrical impedance to pharmacokinetic parameters of theophylline in healthy males.

作者信息

Zarowitz B J, Peterson E, Popovich J

机构信息

Department of Pharmacy Services, Henry Ford Hospital, Detroit, Michigan.

出版信息

Clin Pharmacokinet. 1989 Sep;17(3):200-7. doi: 10.2165/00003088-198917030-00005.

Abstract

Bioelectrical impedance is a reliable, safe, non-invasive and valid method of determining body composition, using measures of resistance and reactance by passing a low voltage alternating current through the body. This study investigates relationships between the pharmacokinetics of theophylline and parameters of bioelectrical impedance in 15 non-smoking, healthy, adult male volunteers. After an overnight fast, subjects received 5 mg/kg of aminophylline intravenously over 30 minutes. Blood samples were obtained serially over a period of 12 hours. Bioelectrical impedance measurements were made in triplicate, using a 4-electrode plethysmograph. Sera were assayed in duplicate by enzyme-mediated immunoassay (coefficient of variation less than 5%), and data were fitted to a non-compartmental regression program. An all-subsets multiple-regression technique was employed to arrive at predictive equations for theophylline clearance (CL) and volume of distribution at steady-state (Vss) using age, height, weight and mean bioelectrical impedance parameters. Equations for Vss and CL revealed p-values of less than 0.001 and coefficients of variation of 8.5 and 13.33% respectively. Although the equations display some degree of colinearity they account for 95 and 86.5% of the variability in Vss and CL respectively, and represent an innovative approach to the estimation of pharmacokinetic parameters.

摘要

生物电阻抗是一种可靠、安全、非侵入性且有效的测定身体成分的方法,它通过让低电压交流电通过身体来测量电阻和电抗。本研究调查了15名不吸烟、健康的成年男性志愿者中茶碱的药代动力学与生物电阻抗参数之间的关系。在禁食过夜后,受试者在30分钟内静脉注射5mg/kg氨茶碱。在12小时内连续采集血样。使用四电极体积描记器对生物电阻抗进行三次测量。血清通过酶介导免疫测定法进行两次测定(变异系数小于5%),数据拟合到非房室回归程序。采用全子集多元回归技术,利用年龄、身高、体重和平均生物电阻抗参数得出茶碱清除率(CL)和稳态分布容积(Vss)的预测方程。Vss和CL的方程显示p值小于0.001,变异系数分别为8.5%和13.33%。尽管这些方程显示出一定程度的共线性,但它们分别解释了Vss和CL中95%和86.5%的变异性,代表了一种估计药代动力学参数的创新方法。

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