Eichelbaum M, Birkel P, Grube E, Gütgemann U, Somogyi A
Klin Wochenschr. 1980 Sep 15;58(18):919-25. doi: 10.1007/BF01477049.
A close relationship between verapamil plasma concentration and effect on P-R interval could be established both after single i.v. and oral administration and during chronic oral treatment. After i.v. administration a linear relationship between verapamil plasma concentration and delta P-R (y=x (0.74) + 1.8) with a small between subject variation in the slope of the regression (%coefficient of variation 18.7, range 0.71-1.10) was observed. The slope of the oral plasma concentration response regression (y=x (0.33)-3.0) was statistically significantly (p less than 0.05) less than the slope of the i.v. plasma level response regression. Interindividual variation in the slope was most pronounced (range 0.13 to 0.47). On average two to three times higher verapamil plasma levels were required after oral administration in order to produce the same increase in delta PR as after intravenous administration. The most plausible explanation for the different slopes of the plasma level response regression seems to be stereo-selective presystemic elimination. Since after oral administration the plasma level response curve is less steep than after i.v. administration this indicates that the more active l-isomer is preferentially metabolized during hepatic first-pass metabolism.
在单次静脉注射和口服给药后以及慢性口服治疗期间,均可确定维拉帕米血浆浓度与对P-R间期的影响之间存在密切关系。静脉注射后,观察到维拉帕米血浆浓度与△P-R之间呈线性关系(y = x(0.74) + 1.8),回归斜率的个体间差异较小(变异系数%为18.7,范围为0.71 - 1.10)。口服血浆浓度反应回归的斜率(y = x(0.33) - 3.0)在统计学上显著低于静脉注射血浆水平反应回归的斜率(p < 0.05)。斜率的个体间差异最为明显(范围为0.13至0.47)。口服给药后,平均需要两到三倍于静脉注射的维拉帕米血浆水平才能产生相同的△PR增加。血浆水平反应回归斜率不同的最合理原因似乎是立体选择性首过消除。由于口服给药后的血浆水平反应曲线比静脉注射后的曲线平缓,这表明活性更强的l-异构体在肝脏首过代谢过程中优先被代谢。