首页> 外文期刊>Journal of Chromatography, Biomedical Applications >Determiantion of methadone and its metabolites EDDP and EMDP in human hair by headspace solid-phase microextraction and gas chromatography-mass spectroemtry
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Determiantion of methadone and its metabolites EDDP and EMDP in human hair by headspace solid-phase microextraction and gas chromatography-mass spectroemtry

机译:顶空固相微萃取-气相色谱-质谱法测定人发中美沙酮及其代谢物EDDP和EMDP

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A simple method for analysis of methadone and its two main metabolites EDDP and EMDP in hair was developed u~ing automatic headspace solid-phase microextractioll (HS-SPME) at a multipurpose sampler and gas chromatography — mass spectrometry with electron impact ionization and selected ion monitoring (GC—MS-SIM). The washed hair pieces were digested in the. closed headspace vial in 1 ml I M NaGH containing 0.5 g NaCi and each 10 ng of the internal standards D9-methadone and D3-EDDP at 1 100C for 20 mm. Then the HS-SPME was performed with a 65 l.i.m polydimethylsilOxafl/ divinylbeazene fiber at the same temperature in the same vial for another 20 mm followed by the desorption in the GC injection port. The calibration curves were linear between 0.1 and 3 ag/mg (methadone and EMDP) and 10 ag/mg (EDDP) respectively, at higher concentrations a negative deviation from linearity was found. The detection limits were 0.03 ng/mg (methadone) and 0.05 ng/mg (EDDP and EMDP), and the reproducibility was 9.2% for methadone and 11.2% for EDDP (n 12). The method was applied to hair samples of 26 drug fatalities. 19 cases were positive with 0.36—11.8 ng/mg methadone and 0.19 —10.8 ng/mg EDDP. EMDP was found only in two cases with 0.18 and 0.84 ng/mg. The methadone concentration range was in agreement with previous data, but the EDDP/methadone concentration ratios (0.19—0.67) were definitely higher than those determined by other methods.
机译:通过在多功能进样器上使用自动顶空固相微萃取(HS-SPME)和气相色谱-电子碰撞电离和选定离子的质谱法,开发了一种分析美沙酮及其两种主要代谢物EDDP和EMDP的简单方法监视(GC-MS-SIM)。将洗过的发丝在其中消化。在1 ml含0.5 g NaCi的I M NaGH和每10 ng内标D9-美沙酮和D3-EDDP中于1100°C封闭的顶空样品瓶,放置20 mm。然后,在同一温度下在同一样品瓶中用65μm的聚二甲基硅氧烷Oxafl /二乙烯基苯氮纤进行HS-SPME再处理20mm,然后在GC进样口中解吸。校准曲线在0.1和3微克/毫克(美沙酮和EMDP)和10微克/毫克(EDDP)之间分别呈线性关系,在较高浓度下,线性线性存在负偏差。检出限为0.03 ng / mg(美沙酮)和0.05 ng / mg(EDDP和EMDP),美沙酮的重现性为9.2%,EDDP为11.2%(n 12)。该方法适用于26种药物死亡的头发样本。美沙酮0.36-11.8 ng / mg和EDDP 0.19-10.8 ng / mg阳性19例。仅在两例中发现EMDP的浓度为0.18和0.84 ng / mg。美沙酮的浓度范围与先前的数据一致,但EDDP /美沙酮的浓度比(0.19-0.67)肯定高于其他方法测定的浓度比。

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