Emanuelsson B M, Persson J, Sandin S, Alm C, Gustafsson L L
Clinical Pharmacology, Clinical Research and Development, Astra Pain Control AB, Södertälje, Sweden.
Ther Drug Monit. 1997 Apr;19(2):126-31. doi: 10.1097/00007691-199704000-00002.
To predict the risk of adverse reactions to local anaesthetics used in clinical practice, it is crucial to know whether any nonlinearity exists in their pharmacokinetics. The disposition of ropivacaine, a new local anesthetic agent, was evaluated in healthy subjects on the basis of plasma levels in the concentration range obtained after regional anaesthesia. Three intravenous doses of ropivacaine hydrochloride (20, 40, and 80 mg) were given in a double-blind, randomized, complete crossover design. Analysis of variance was used to assess the importance of intra- versus interindividual variability in the basic pharmacokinetics. The mean plasma clearance (400 ml/min), volume of distribution at steady state (40 l), and terminal half-life (1.7 h) were similar, irrespective of dose. The intersubject variability for these parameters was higher than the intrasubject variability. A slight increase in free fraction (15%) with increasing dose might indicate that the lower limit for saturation of protein binding may be reached at the higher plasma levels. One subject (80 mg) reported numbness of the lower lip 2 min after the end of the infusion, which may be a sign of systemic CNS toxicity. The total and free plasma concentration was extrapolated to 1.7 and 0.08 mg/l, respectively.
为预测临床实践中使用的局部麻醉药的不良反应风险,了解其药代动力学中是否存在任何非线性关系至关重要。基于区域麻醉后获得的浓度范围内的血浆水平,在健康受试者中评估了一种新型局部麻醉药罗哌卡因的处置情况。采用双盲、随机、完全交叉设计给予三剂静脉注射盐酸罗哌卡因(20、40和80毫克)。方差分析用于评估个体内与个体间变异性在基本药代动力学中的重要性。无论剂量如何,平均血浆清除率(400毫升/分钟)、稳态分布容积(40升)和终末半衰期(1.7小时)均相似。这些参数的个体间变异性高于个体内变异性。随着剂量增加,游离分数略有增加(15%),这可能表明在较高血浆水平时可能达到蛋白质结合饱和的下限。一名受试者(80毫克)在输注结束后2分钟报告下唇麻木,这可能是全身中枢神经系统毒性的迹象。总血浆浓度和游离血浆浓度分别外推至1.7毫克/升和0.08毫克/升。