Tilstone W J, Lawson D H
Res Commun Chem Pathol Pharmacol. 1978 Aug;21(2):343-6.
Procainamide (PA) pharmacokinetics were studied at steady state in 19 patients. The PA was given as 1.0 or 1.5 g eight hourly (L and H dose groups) and acetylator phenotype determined from sulphadimidine acetylation was classified as Slow or Fast (S or F). Thus, four groups were categorized, HF, LF, HS and LS with 7, 5, 3, and 4 patients in each respective group. Overall the mean steady state plasma concentration of PA (Cpss) expressed as a fraction of dose did not depend on dose or on acetylator status, but the HS group had significantly higher Cpss per gram dose (6.3 mug/ml) than LS (2.7 mug/ml) or the HF (2.3 mug/ml) groups. Clearance of PA be acetylation (C1A) was 23.8% of the total in fast acetylators and 16.5% in slow acetylators. C1A was not dose-dependent in the HF or LF groups (mean 177.9 ml/min and 168.4 ml/min) but was dose-dependent in the HS group (mean 74.6 ml/min) which differed significantly from the LS group (mean 113.4 ml/min).
在19名患者中研究了普鲁卡因胺(PA)在稳态时的药代动力学。PA以每8小时1.0或1.5克的剂量给药(高剂量组和低剂量组),根据磺胺二甲嘧啶乙酰化确定的乙酰化表型分为慢乙酰化型或快乙酰化型(S或F)。因此,分为四组,即HF、LF、HS和LS组,每组分别有7、5、3和4名患者。总体而言,以剂量分数表示的PA平均稳态血浆浓度(Cpss)不依赖于剂量或乙酰化状态,但HS组每克剂量的Cpss(6.3μg/ml)显著高于LS组(2.7μg/ml)或HF组(2.3μg/ml)。通过乙酰化作用的PA清除率(C1A)在快乙酰化者中占总量的23.8%,在慢乙酰化者中占16.5%。在HF或LF组中,C1A不依赖于剂量(平均分别为177.9ml/min和168.4ml/min),但在HS组中C1A依赖于剂量(平均74.6ml/min),且与LS组(平均113.4ml/min)有显著差异。