首页> 外文期刊>Journal of Analytical Toxicology >GC-MS Quantitation of Codeine, Morphine, 6-Acetylmorphine, Hydrocodone, Hydromorphone, Oxycodone, and Oxymorphone in Blood.
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GC-MS Quantitation of Codeine, Morphine, 6-Acetylmorphine, Hydrocodone, Hydromorphone, Oxycodone, and Oxymorphone in Blood.

机译:血液中可待因,吗啡,6-乙酰吗啡,氢可酮,氢吗啡酮,羟考酮和羟吗啡酮的GC-MS定量分析。

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A method is described for the simultaneous analysis of seven opiates, codeine, morphine, 6-acetylmorphine, hydrocodone, hydromorphone, oxycodone, and oxymorphone, in blood samples by gas chromatography-mass spectrometry (GC-MS). One milliliter of blood is combined with an internal standard mixture containing 200 ng of each of the seven deuterated opiates. Two milliliters of acetonitrile is added to precipitate the proteins and cellular material. After centrifugation, the clear supernatant is removed, and the acetonitrile is evaporated. The remaining aqueous portion is adjusted to pH 9 with sodium bicarbonate buffer, and the drugs are extracted into chloroform/ trifluoroethanol (10:1). The organic extractant is transferred and dried under nitrogen. The residue is reconstituted in dilute hydrochloric acid and washed consecutively with hexane and chloroform. The purified aqueous portion is adjusted to pH 9 with bicarbonate buffer, and the drugs are again extracted into chloroform/trifluoroethanol (10:1). The organic portion is removed from the aqueous fraction and dried under nitrogen. The residue is consecutively derivatized with methoxyamine and propionic anhydride using pyridine as a catalyst. The ketone groups on hydrocodone, hydromorphone, oxycodone, and oxymorphone are converted to methoximes. Hydroxyl groups present at the O3 and O6 positions of codeine, morphine, 6-acetylmorphine, hydromorphone, and oxymorphone are converted to their respective propionyl esters. After a post-derivatization purification step, the extracts are analyzed by full scan GC-MS using electron impact ionization. The method is linear to at least 2000 ng/mL. Day-to-day precision (N = 15) at 500 ng/mL and 75 ng/mL were less than 10% for all seven targeted opiates. Extraction efficiencies at these two concentrations ranged from 50% to 68%. For each opiate, the limit of quantitation was 10 ng/mL, and the limit of detection was 2 ng/mL.
机译:描述了一种通过气相色谱-质谱法(GC-MS)同时分析血液样品中的七个鸦片,可待因,吗啡,6-乙酰吗啡,氢可酮,氢吗啡酮,羟考酮和羟吗啡酮的方法。将一毫升血液与内标混合物混合,内标混合物含有200 ng七种氘代阿片类药物中的每一种。加入两毫升乙腈以沉淀蛋白质和细胞物质。离心后,除去澄清的上清液,并蒸发乙腈。用碳酸氢钠缓冲液将剩余的水部分调节至pH 9,并将药物萃取至氯仿/三氟乙醇(10:1)中。转移有机萃取剂,并在氮气下干燥。将残余物在稀盐酸中重构,并依次用己烷和氯仿洗涤。用碳酸氢盐缓冲液将纯化的水部分的pH调节至9,然后将药物再次萃取至氯仿/三氟乙醇(10:1)中。从含水部分中除去有机部分,并在氮气下干燥。使用吡啶作为催化剂,用甲氧基胺和丙酸酐将残余物连续衍生。氢可酮,氢吗啡酮,羟考酮和羟吗啡酮上的酮基被转化为甲肟。可待因,吗啡,6-乙酰基吗啡,氢吗啡酮和羟吗啡酮的O3和O6位置上存在的羟基被转化为它们各自的丙酸酯。衍生化后的纯化步骤后,使用电子碰撞电离通过全扫描GC-MS分析提取物。该方法线性至少为2000 ng / mL。对于所有7种靶向鸦片制剂,其500 ng / mL和75 ng / mL的日常精密度(N = 15)均低于10%。这两种浓度下的萃取效率范围为50%至68%。对于每种鸦片制剂,定量限为10 ng / mL,检出限为2 ng / mL。

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