Egan T D, Lemmens H J, Fiset P, Hermann D J, Muir K T, Stanski D R, Shafer S L
Department of Anesthesiology, University of Utah School of Medicine, Salt Lake City 84132.
Anesthesiology. 1993 Nov;79(5):881-92. doi: 10.1097/00000542-199311000-00004.
Remifentanil (GI87084B) is a new short-acting opioid with a unique ester structure. Metabolism of remifentanil by ester hydrolysis results in very rapid elimination. The aim of this study was to characterize in detail the pharmacokinetic profile of remifentanil in healthy male volunteers.
Ten healthy adult male volunteers received a zero-order infusion of remifentanil at doses ranging from 1 to 8 micrograms.kg-1.min-1 for 20 min. Frequent arterial blood samples were drawn and analyzed by gas chromatographic mass spectroscopy to determine the remifentanil blood concentrations. The raw pharmacokinetic data were analyzed using three different parametric compartmental modeling methods (traditional two-stage, naive pooled data, and NONMEM). The raw pharmacokinetic data also were analyzed using numeric deconvolution and a nonparametric moment technique. A computer simulation using hte pharmacokinetic parameters of the NONMEM compartmental model was performed to provide a more intuitively meaningful and clinically relevant description of the pharmacokinetics. The simulation estimated the time necessary to achieve a 50% decrease in remifentanil concentration after a variable-length infusion.
For each parametric method, a three-compartment mamillary model that accurately describes remifentanil's concentration decay curve was constructed. The NONMEM analysis population pharmacokinetic parameters included a central clearance of 2.8 l/min, a volume of distribution at steady state of 32.8 l, and a terminal half-life of 48 min. The mean results of the nonparametric moment analysis included a clearance of 2.9 l/min, a volume of distribution at steady state of 31.8 l, and a mean residence time of 10.9 min. The computer simulation revealed the strikingly unique pharmacokinetic profile of remifentanil compared to that of the currently available fentanyl family of opioids.
Remifentanil is a new, short-acting opioid with promising clinical potential in anesthesiology.
瑞芬太尼(GI87084B)是一种新型短效阿片类药物,具有独特的酯结构。瑞芬太尼通过酯水解代谢,导致其快速消除。本研究的目的是详细描述瑞芬太尼在健康男性志愿者中的药代动力学特征。
10名健康成年男性志愿者接受零级输注瑞芬太尼,剂量范围为1至8微克·千克⁻¹·分钟⁻¹,持续20分钟。频繁采集动脉血样,并用气相色谱-质谱分析法进行分析,以测定瑞芬太尼的血药浓度。使用三种不同的参数房室模型方法(传统两阶段法、单纯合并数据法和NONMEM法)分析原始药代动力学数据。原始药代动力学数据还使用数值反卷积和非参数矩技术进行分析。利用NONMEM房室模型的药代动力学参数进行计算机模拟,以提供更直观且与临床相关的药代动力学描述。该模拟估计了在可变长度输注后瑞芬太尼浓度降低50%所需的时间。
对于每种参数方法,均构建了一个能准确描述瑞芬太尼浓度衰减曲线的三室乳突模型。NONMEM分析的群体药代动力学参数包括中央清除率为2.8升/分钟、稳态分布容积为32.8升以及末端半衰期为48分钟。非参数矩分析的平均结果包括清除率为2.9升/分钟、稳态分布容积为31.8升以及平均驻留时间为10.9分钟。计算机模拟显示,与目前可用的芬太尼类阿片类药物相比,瑞芬太尼具有极其独特的药代动力学特征。
瑞芬太尼是一种新型短效阿片类药物,在麻醉学领域具有广阔的临床应用潜力。