Ward S, Boheimer N, Weatherley B C, Simmonds R J, Dopson T A
Br J Anaesth. 1987 Jun;59(6):697-706. doi: 10.1093/bja/59.6.697.
The plasma pharmacokinetic profiles of atracurium and its derivatives, laudanosine and monoquaternary alcohol, were studied in six patients with renal failure after a bolus dose of atracurium 0.3-0.4 mg kg-1. The pharmacokinetics of the derivatives only were studied in a group of four normal patients receiving atracurium 0.3 mg kg-1. Measurements of plasma and urine concentrations were performed by high pressure liquid chromatography. Pharmacokinetics of atracurium were not significantly different in the renal failure group when compared with those obtained in a previous study on six normal patients. Although 2-10% of the dose was recovered in the urine of normal patients as unchanged atracurium, and 3-4% as laudanosine, renal failure produced no significant differences in plasma pharmacokinetics, with mean plasma elimination half-lives of 20 min for atracurium, 234 min for laudanosine and 39 min for quaternary alcohol.
在6例肾衰竭患者静脉注射0.3 - 0.4mg/kg阿曲库铵后,研究了阿曲库铵及其衍生物劳丹诺辛和单季铵醇的血浆药代动力学特征。仅在一组4例接受0.3mg/kg阿曲库铵的正常患者中研究了衍生物的药代动力学。采用高压液相色谱法测定血浆和尿液浓度。与之前对6例正常患者的研究相比,肾衰竭组阿曲库铵的药代动力学无显著差异。尽管在正常患者尿液中可回收2 - 10%未变化的阿曲库铵剂量,3 - 4%为劳丹诺辛,但肾衰竭对血浆药代动力学无显著影响,阿曲库铵的平均血浆消除半衰期为20分钟,劳丹诺辛为234分钟,季铵醇为39分钟。