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使用逆向透析进行体外和体内微透析校准以研究布比卡因的脑脊液分布。

In vitro and in vivo microdialysis calibration using retrodialysis for the study of the cerebrospinal distribution of bupivacaine.

作者信息

Clément R, Malinovsky J M, Dollo G, Le Corre P, Chevanne F, Le Verge R

机构信息

Laboratoire de Pharmacie Galénique, Biopharmacie et Pharmacie Clinique, Faculté des Sciences Pharmaceutiques et Biologiques, Rennes, France.

出版信息

J Pharm Biomed Anal. 1998 Aug;17(4-5):665-70. doi: 10.1016/s0731-7085(97)00274-4.

Abstract

Microdialysis coupled to HPLC was used to study the disposition of local anesthetics in the cerebrospinal fluid (CSF) because of the difficulty in sampling CSF. A retrodialysis method for the microdialysis calibration was investigated in vitro and in vivo. Calibration by retrodialysis was simultaneously validated through the use of the zero net flux method. Two local anesthetics (bupivacaine and ropivacaine), which differ structurally by only one methyl group, were respectively utilized as substance of interest and as internal standard. Different parameters were tested in vitro to compare the relative recovery (RR) of bupivacaine and the relative loss (RL) of ropivacaine. Several flow rates were tried to select an optimal in vivo flow rate (1 microliter/min). the RR and RL values were not influenced by the variation of bupivacaine concentration. A significant variability among different probes within a batch was established (RR ranging from 41.1-65.3%; RL ranging from 30.7-61.0%). The K-factor values, defined as RLropivacaine/RLbupivacaine, were calculated in vitro and in vivo. This ratio decreased in vivo but was constant (K in vitro = 1.06 +/- 0.04, K in vivo = 0.87 +/- 0.03). The extracellular tissue concentration of the compound of interest was again in vitro and no deterioration of probe during the in vivo experiment was found. After administration of bupivacaine in the epidural space of rabbits, plasma and microdialysis CSF samples were simultaneously collected. Plasma and CSF disposition of bupivacaine displayed different kinetics. The maximum CSF concentration of B averaged 394 +/- 170 micrograms ml-1 with a mean Tmax of 3.8 +/- 1.8 min. The maximum CSF concentration of B averaged 0.44 +/- 0.09 micrograms ml-1 with a mean Tmax occurring at 1 min. Microdialysis, combined with accurate calibration, should be a reliable technique to gain further insight in the spinal disposition of local anesthetics.

摘要

由于脑脊液(CSF)采样困难,采用微透析与高效液相色谱联用的方法来研究局部麻醉药在脑脊液中的分布情况。在体外和体内研究了一种用于微透析校准的逆向透析方法。通过使用零净通量法同时验证了逆向透析校准。两种仅在结构上相差一个甲基的局部麻醉药(布比卡因和罗哌卡因)分别用作目标物质和内标。在体外测试了不同参数,以比较布比卡因的相对回收率(RR)和罗哌卡因的相对损失率(RL)。尝试了几种流速以选择最佳的体内流速(1微升/分钟)。RR和RL值不受布比卡因浓度变化的影响。确定了一批不同探针之间存在显著差异(RR范围为41.1 - 65.3%;RL范围为30.7 - 61.0%)。计算了体外和体内定义为RL罗哌卡因/RL布比卡因的K因子值。该比率在体内降低但保持恒定(体外K = 1.06 ± 0.04,体内K = 0.87 ± 0.03)。目标化合物的细胞外组织浓度再次在体外进行了测定,并且在体内实验期间未发现探针变质。在兔硬膜外腔给予布比卡因后,同时采集血浆和微透析脑脊液样本。布比卡因在血浆和脑脊液中的分布呈现不同的动力学。布比卡因的最大脑脊液浓度平均为394 ± 170微克/毫升,平均达峰时间为3.8 ± 1.8分钟。罗哌卡因的最大脑脊液浓度平均为0.44 ± 0.09微克/毫升,平均达峰时间出现在1分钟。微透析结合精确校准,应该是一种可靠的技术,有助于进一步深入了解局部麻醉药在脊髓中的分布情况。

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