Coyle D E, Denson D D
Ther Drug Monit. 1986;8(1):98-101. doi: 10.1097/00007691-198603000-00016.
A gas-liquid chromatographic method for the simultaneous measurement of bupivacaine, etidocaine, lidocaine, meperidine, mepivacaine, and methadone in serum is described. The drugs and the internal standard, prilocaine, are extracted from 1 ml of serum. The procedure involves a two-step extraction and injection of the extract into a gas chromatograph equipped with a 10-ft OV-11 glass column and a nitrogen-phosphorus detector. The temperature gradient program results in a run time of 16 min and retention times for meperidine, prilocaine (internal standard), lidocaine, etidocaine, mepivacaine, methadone, and bupivacaine of 3.8, 5.4, 6.0, 8.7, 11.0, 11.7, and 14.8 min, respectively. Standard curves for all drugs were linear over the 80 to 2,000-ng/ml range and recovery of all components averaged 97 +/- 2% with the lowest detection limit of 10 ng/ml for all drugs except meperidine and methadone, which were 20 ng/ml. The within-day coefficients of variation ranged from 12 to 8% at 500 ng/ml. The day-to-day coefficients of variation of the slope and intercept values ranged from 2 to 0% and 130 to 3%, respectively. Response factors of the nitrogen-specific collector varied with the drug analyzed and resulted in peak area variation at constant offset and attenuation of 30%. This method is intended and adequate for therapeutic monitoring of chronically treated pain patients who are being given various combinations of local anesthetic and/or narcotic agents.
本文描述了一种气相色谱法,用于同时测定血清中的布比卡因、依替卡因、利多卡因、哌替啶、甲哌卡因和美沙酮。从1ml血清中提取这些药物和内标药丙胺卡因。该过程包括两步萃取,并将萃取物注入配备10英尺OV-11玻璃柱和氮磷检测器的气相色谱仪中。温度梯度程序使运行时间为16分钟,哌替啶、丙胺卡因(内标)、利多卡因、依替卡因、甲哌卡因、美沙酮和布比卡因的保留时间分别为3.8、5.4、6.0、8.7、11.0、11.7和14.8分钟。所有药物的标准曲线在80至2000 ng/ml范围内呈线性,所有成分的回收率平均为97±2%,除哌替啶和美沙酮的最低检测限为20 ng/ml外,其他所有药物的最低检测限为10 ng/ml。日内变异系数在500 ng/ml时为12%至8%。斜率和截距值的日间变异系数分别为2%至0%和130%至3%。氮特异性收集器的响应因子因所分析的药物而异,导致在恒定偏移和30%衰减情况下峰面积发生变化。该方法适用于对长期接受局部麻醉剂和/或麻醉剂各种组合治疗的疼痛患者进行治疗监测。