毛发中阿片类药物毛细管电泳分析提取方法的关键比较。

Elizabete C de Lima, Clóvis L da Silva, Magnólia L N Gauchée, Marina F M Tavares
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引用次数: 0

摘要

本文介绍了毛细管分析人类头发中7种阿片类药物(哌替啶、吗啡、纳洛酮、曲马多、芬太尼、舒芬太尼和阿芬太尼)的提取方法的比较评价。将头发(50-150 mg)进行酸性水解(0.25 mmol L(-1) HCl, 45℃,过夜),然后调整pH值,在正己烷、石油醚、二氯甲烷和乙酸乙酯溶剂中进行液-液萃取(LLE),或在十八烷基、氰丙基和氨基丙基键合二氧化硅和阳离子交换聚合物相中进行固相萃取(SPE)。在m固定模式阳离子交换反相药盒(Oasis MCX LP, Waters Corp., Milford, MA, U.S.A.)中使用SPE获得了约70%(纳洛酮和芬太尼及其类似物)、88%(哌替啶)和约100%(吗啡和曲马多)的极好回收率,使这种类型的程序符合用于头发分析的新型临床和法医方法的要求。通过对使用吗啡作为疼痛管理方案一部分的患者的头发提取物的分析,证明了所提出的提取技术的实用性。
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Critical comparison of extraction procedures for the capillary electrophoretic analysis of opiates in hair.

This work presents a comparative evaluation of extraction procedures for the capillary analysis of seven opiates (meperidine, morphine, naloxone, tramadol, fentanyl, sufentanyl, and alfentanyl) in human hair. Pieces of hair (50-150 mg) were subjected to acidic hydrolysis (0.25 mmol L(-1) HCl at 45 degrees C, overnight) followed by pH adjustment and either liquid-liquid extraction (LLE) in hexane, petroleum ether, dichloromethane, and ethyl acetate solvents, or solid-phase extraction (SPE) in octadecyl, cyanopropyl, and aminopropyl bonded silica and cation exchange polymeric phases. Excellent recoveries of approximately 70% (naloxone and fentanyl and its analogues), 88% (meperidine), and ca. 100% (morphine and tramadol) were obtained using SPE in a M-fixed-mode cation exchange reversed-phase cartridge (Oasis MCX LP, Waters Corp., Milford, MA, U.S.A.), making this type of procedure eligible for novel clinical and forensic methodologies for hair analysis. The utility of the proposed extraction technique was demonstrated by the analysis of hair extracts from patients using morphine as part of their pain management protocol.

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