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中国临床药理学与治疗学 ›› 2008, Vol. 13 ›› Issue (7): 809-812.

• 短篇报道 • 上一篇    下一篇

复合全麻下罗哌卡因硬膜外阻滞的药代动力学

祝永明1, 肖旺频1, 安尔丹1, 周清河1, 涂厉标1, 楼洪刚2   

  1. 1浙江省嘉兴学院附属第二医院, 嘉兴 314000, 浙江;
    2浙江大学医学院附属第二医院, 杭州 310009, 浙江
  • 收稿日期:2008-03-11 修回日期:2008-05-25 出版日期:2008-07-26 发布日期:2020-10-14
  • 作者简介:祝永明,男,硕士,副主任药师,主要从事医院临床药学研究。Tel:0573-82031907 E-mail:ymzhujx@hotmail.com
  • 基金资助:
    浙江省嘉兴市科技局科技计划项目(2005AY3026)

Pharmacokinetics of ropivacaine during epidural block combined with general anesthesia

ZHU Yong-ming1, XIAO Wang-pin1, AN Er-dan1, ZHOU Qing-he1, TU Li-biao1, LOU Honggang2   

  1. 1Second Affiliated Hospital of Jiaxing College of Zhejiang Province, Jiaxing 314000, Zhejiang, China;
    2Second Affiliated Hospital of Medical College of Zhejiang University, Hangzhou 310009, Zhejiang, China
  • Received:2008-03-11 Revised:2008-05-25 Online:2008-07-26 Published:2020-10-14

摘要: 目的:对罗哌卡因硬膜外阻滞复合全麻的手术病人进行药代动力学研究。方法:选择12例上腹部手术病人,硬膜外腔注入0.5%罗哌卡因,并行全麻诱导,于输入罗哌卡因后1、10、20、30、45、60、75、90、120、150、180min分别从左桡动脉采血,用高效液相色谱仪测定罗哌卡因血药浓度,用DAS2.0药动学统计软件拟合房室模型,并计算各项药代动力学参数。结果:术中、术后均未见与罗哌卡因有关的不良反应,罗哌卡因的主要药代动力学参数:tmax为10min;Cmax为0.713mgL;t1/2α为122min;t1/2β为190min;AUC0→180为(72±10)μg·mL-1·min-1结论:复合全麻下罗哌卡因硬膜外阻滞药物代谢符合二室模型,安全性良好,镇痛效果满意。

关键词: 罗哌卡因, 药代动力学, 硬膜外阻滞, 复合全麻

Abstract: AIM: To study the pharmacokinetics characteristics of patients who used ropivacaine epidural block with general anesthesia.METHODS: Twelve patients scheduled for upper abdominal surgery were included in this study.0.5% ropivacaine was injected into epidural space before general anesthesia.Blood samples were taken from left radial artery at 1, 10, 20, 30, 45, 60, 75, 90, 120, 150 and 180 min after injecting ropivacaine.The plasma concentration of ropivacaine was determined by HPLC.The Compartment model was fitted by DAS statistics software, and the pharmacokinetic parameters were calculated.RESULTS: There were no adverse effects about ropivacaine during and after operation.The main pharmacokinetic parameters were as follow: tmax was 10 min;Cmax was 0.713mg/L; t1/2α was 122 min;t1/2β was 190 min;AUC0→180 was (72±10)μg·mL-1·min-1.CONCLUSION: The concentration-time curves were fitted to two-compartment open pharmacokinetic model.0.5% ropivacaine was proved to be safe, and it had good analgesia effect.

Key words: ropivacaine, pharmacokinetics, epidural block, combined with general anesthesia

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