Höld K M, Wilkins D G, Rollins D E, Joseph R E, Cone E J
Department of Pharmacology and Toxicology, University of Utah, Salt Lake City 84112, USA.
J Chromatogr Sci. 1998 Mar;36(3):125-30. doi: 10.1093/chromsci/36.3.125.
A sensitive method is developed for the combined extraction of cocaine (COC), cocaethylene (CE), benzoylecgonine (BE), ecgonine methyl ester (EME), norcocaine (NORCOC), 6-acetylmorphine (6-MAM), codeine (COD), norcodeine (NORCOD), morphine (MOR), and normorphine (NORMOR) from human head hair using an enzyme-based digestion technique (Protease VIII/DTT/Tris-buffer pH 6.5 at 22 degrees C). After pH adjustment to 5.5, the digests are extracted with a solid-phase extraction procedure using Bond-Elut Certify columns. The extract residues are evaporated at 40 degrees C, reconstituted in 20 microL of ethyl acetate, and derivatized with the reagents N-methyl-N-trimethylsilylheptafluorobutyramide (MSHFBA), N-methyl-bis-heptafluorobutyramide (MBHFBA), and N-trimethylsilylimidazole (TMSIM). Analyses are performed by positive ion chemical ionization gas chromatography-mass spectrometry using a DB-1 capillary column. Two injections are performed on each extract to optimize sensitivity for all analytes. The assay is capable of reliably quantitating 500 pg/mg of all compounds and is linear to 50 ng/mg, except for BE, which is linear to 25.0 ng/mg. The method was used to analyze human hair samples obtained from cocaine and heroin users. COC, BE, and EME are detectable in all samples, whereas NORCOC, CE, COD, 6-MAM, and MOR are detected in only some samples. Norcodeine and normorphine are not detected. The assay is currently being used to analyze hair samples from a study investigating the mechanisms of drug disposition in hair.
开发了一种灵敏的方法,使用基于酶的消化技术(在22摄氏度下,蛋白酶VIII/二硫苏糖醇/ pH 6.5的Tris缓冲液)从人头发中联合提取可卡因(COC)、可口卡因(CE)、苯甲酰爱康宁(BE)、芽子碱甲酯(EME)、去甲可卡因(NORCOC)、6-乙酰吗啡(6-MAM)、可待因(COD)、去甲可待因(NORCOD)、吗啡(MOR)和去甲吗啡(NORMOR)。将消化液的pH值调至5.5后,使用Bond-Elut Certify柱通过固相萃取程序进行萃取。萃取残留物在40摄氏度下蒸发,用20微升乙酸乙酯复溶,并用N-甲基-N-三甲基硅烷基七氟丁酰胺(MSHFBA)、N-甲基-双-七氟丁酰胺(MBHFBA)和N-三甲基硅烷基咪唑(TMSIM)试剂进行衍生化。使用DB-1毛细管柱通过正离子化学电离气相色谱-质谱法进行分析。对每个提取物进行两次进样,以优化所有分析物的灵敏度。该测定法能够可靠地定量所有化合物500 pg/mg,并且在50 ng/mg范围内呈线性,除了BE在25.0 ng/mg范围内呈线性。该方法用于分析从可卡因和海洛因使用者处获得的人发样本。在所有样本中均可检测到COC、BE和EME,而仅在一些样本中检测到NORCOC、CE、COD、6-MAM和MOR。未检测到去甲可待因和去甲吗啡。该测定法目前正用于分析一项研究的头发样本,该研究旨在探究药物在头发中的处置机制。