Mahmood I
Office of clinical Pharmacology and Biopharmaceutics, Food and Drug Administration, Rockville, MD 20852, USA.
Am J Ther. 1998 Nov;5(6):377-81. doi: 10.1097/00045391-199811000-00004.
This article describes a simple method for the estimation of absorption rate constant (ka ) after oral administration and compares the proposed method with some of the existing methods. The proposed method is based on a previous work of Urso and Aarons known as the regression method of truncated areas for the estimation of absolute bioavailability for drugs with a long elimination half-life. The following equation was used to estimate ka : Y(t) = ka. F - ka. X(t). Simple linear regression of Y(t) on X(t) results in a straight line with a slope of -ka, intercept on y-axis of ka F, and abscissa intercept F (absolute bioavailability). Different sets of plasma concentration versus time data for a hypothetical drug were generated by simulation. The estimated ka from the proposed method was compared with the Wagner-Nelson, Loo-Riegelman, and statistical moments methods. The results of this study indicated that the proposed regression method performed satisfactorily for a hypothetical drug that follows a one-compartment or two-compartment model with short or long half-life when tested under variable conditions (different absorption and elimination rate constants). The regression method of truncated areas can be used for the accurate estimation of ka for both short and long half-life drugs.
本文介绍了一种口服给药后吸收速率常数(ka)的简单估算方法,并将该方法与一些现有方法进行了比较。所提出的方法基于乌尔索(Urso)和阿伦斯(Aarons)之前的一项工作,即截断面积回归法,用于估算消除半衰期较长药物的绝对生物利用度。使用以下方程估算ka:Y(t)=ka·F - ka·X(t)。Y(t)对X(t)进行简单线性回归,得到一条直线,其斜率为-ka,y轴截距为ka F,横坐标截距为F(绝对生物利用度)。通过模拟生成了一种假设药物的不同血浆浓度-时间数据集。将所提出方法估算的ka与瓦格纳-尼尔森(Wagner-Nelson)法、卢-里格尔曼(Loo-Riegelman)法和统计矩法进行了比较。本研究结果表明,当在可变条件(不同的吸收和消除速率常数)下进行测试时,所提出的回归法对于遵循单室或双室模型、半衰期短或长的假设药物表现令人满意。截断面积回归法可用于准确估算半衰期短和长的药物的ka。