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鞘内注射吗啡和哌替啶在人体中的药代动力学。

Pharmacokinetics of intrathecal morphine and meperidine in humans.

作者信息

Sjöström S, Tamsen A, Persson M P, Hartvig P

机构信息

Department of Anesthesiology, University Hospital, Uppsala, Sweden.

出版信息

Anesthesiology. 1987 Dec;67(6):889-95. doi: 10.1097/00000542-198712000-00003.

Abstract

Two groups of surgical patients each comprising six individuals received an intrathecal injection of morphine 0.3 mg or meperidine 10 mg. Cerebrospinal fluid (CSF) and plasma were sampled frequently during a 6-h period and analyzed for morphine or meperidine. Maximum plasma morphine concentrations were found 5-10 min after injection, and averaged 4.5 +/- 1.1 ng.ml-1 (mean +/- SEM). Maximum CSF morphine concentrations were considerably higher than maximum plasma concentrations, 6410 +/- 1290 ng.ml-1. Maximum plasma concentrations of meperidine were also measured 5 or 10 min after injection and were low (36 +/- 9 ng.ml-1) compared with the maximum CSF concentrations (364 +/- 105 micrograms.ml-1). After a rapid initial decline for about 15 min after injection, the CSF concentrations decreased with a half-life of 89.8 +/- 16.1 min for morphine and 68.0 +/- 5.1 min for meperidine during the rest of the study period. The initial volume of distribution in CSF was similar for both drugs, or 22 +/- 8 ml for morphine and 18 +/- 5 ml for meperidine. After 6 h, 1.6 +/- 0.9% of the injected morphine dose and 0.41 +/- 0.09% of the meperidine dose remained in the initial volume of distribution. Large inter-individual differences in morphine and meperidine CSF kinetics existed, which may explain some of the reported individual differences in duration of effects. The disappearance of meperidine from CSF tended to be faster than that of morphine, which may be explained, in part, by the differences in lipid solubilities of the drugs.

摘要

两组外科手术患者各有6人,分别接受了0.3毫克吗啡或10毫克哌替啶的鞘内注射。在6小时内频繁采集脑脊液(CSF)和血浆样本,并分析其中的吗啡或哌替啶。注射后5 - 10分钟测得血浆吗啡最大浓度,平均为4.5±1.1纳克/毫升(均值±标准误)。脑脊液吗啡最大浓度显著高于血浆最大浓度,为6410±1290纳克/毫升。哌替啶的血浆最大浓度也在注射后5或10分钟测得,与脑脊液最大浓度(364±105微克/毫升)相比很低(36±9纳克/毫升)。注射后最初15分钟左右迅速下降,在研究剩余期间,脑脊液中吗啡浓度以89.8±16.1分钟的半衰期下降,哌替啶以68.0±5.1分钟的半衰期下降。两种药物在脑脊液中的初始分布容积相似,吗啡为22±8毫升,哌替啶为18±5毫升。6小时后,注射的吗啡剂量的1.6±0.9%和哌替啶剂量的0.41±0.09%仍留在初始分布容积中。吗啡和哌替啶在脑脊液中的动力学存在较大个体差异,这可能解释了一些报道的效应持续时间的个体差异。哌替啶从脑脊液中的消失往往比吗啡快,这部分可以用药物脂溶性的差异来解释。

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