Christensen E B, Hansen S H, Rasmussen S N
Department of Biological Sciences, Royal Danish School of Pharmacy, Copenhagen, Denmark.
Chirality. 1995;7(3):163-6. doi: 10.1002/chir.530070310.
The extent of myocardial accumulation of tocainide, administered as single enantiomers and as well as racemate, was determined in the isolated, spontaneous beating rabbit heart. The heart was retrogradely perfused at a constant rate and fractions of the perfusate were collected during and after infusion. Kinetic parameters for myocardial accumulation and disposition of tocainide were indirectly determined from drug concentration/time course in the outflow perfusate. No stereoselectivity in myocardial accumulation was observed. A two compartment model with mean half-lives for distribution and elimination of 0.60 and 3.78 min, respectively, was fitted to the accumulation and disposition data. At steady-state, tocainide enantiomers were accumulated about three times in the myocardium relative to the perfusion liquid.
在离体、自发搏动的兔心脏中测定了作为单一对映体以及外消旋体给药的妥卡尼在心肌中的蓄积程度。心脏以恒定速率逆行灌注,并在输注期间和之后收集灌注液的部分样本。根据流出灌注液中药物浓度/时间过程间接确定妥卡尼在心肌中的蓄积和处置动力学参数。未观察到心肌蓄积中的立体选择性。将一个具有平均分布半衰期和消除半衰期分别为0.60分钟和3.78分钟的二室模型拟合到蓄积和处置数据。在稳态时,相对于灌注液,妥卡尼对映体在心肌中的蓄积约为三倍。