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Synthesis and bioanalytical evaluation of morphine-3-O-sulfate and morphine-6-O-sulfate in human urine and plasma using LC-MS/MS

机译:LC-MS / MS法测定人尿液和血浆中3-O-硫酸吗啡和-6-O-吗啡的合成及生物分析

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The aim of this work was to synthesize morphine-3-O-sulfate and morphine-6-O-sulfate for use as reference substances, and to determine the sulfate conjugates as possible heroin and morphine metabolites in plasma and urine by a validated LC-MS/MS method. Morphine-6-O-sulfate and morphine-3-O-sulfate were prepared as dihydrates from morphine hydrochloride, in overall yields of 41 and 39% with product purities of >99.5% and >98%, respectively. For bioanalysis, the chromatographic system consisted of a reversed-phase column and gradient elution. The tandem mass spectrometer was operated in the positive electrospray mode using selected reaction monitoring, of transition m/z 366.15 to 286.40. The measuring range was 5-500 ng/mL for morphine-3-O-sulfate and 4.5-454 ng/mL for morphine-6-O-sulfate in plasma. In urine, the measuring range was 50-5000 ng/mL for morphine-3-O-sulfate and 45.4-4544 ng/mL for morphine-6-O-sulfate. The intra-assay and total imprecision (coefficient of variation) was below 11% for both analytes in urine and plasma. Quantifiable levels of morphine-3-O-sulfate in authentic urine and plasma samples were found. Only one authentic urine sample contained a detectable level of morphine-6-O-sulfate, while no detectable morphine-6-O-sulfate was found in plasma samples.
机译:这项工作的目的是合成用作参考物质的3-O-吗啡硫酸盐和-6-O-吗啡硫酸盐,并通过经过验证的LC-HPLC确定血浆和尿液中硫酸盐结合物作为海洛因和吗啡代谢物的可能含量。 MS / MS方法。从盐酸吗啡以二水合物形式制备吗啡-6-O-硫酸盐和吗啡-3-O-硫酸盐,总收率分别为41%和39%,产品纯度分别> 99.5%和> 98%。对于生物分析,色谱系统由反相柱和梯度洗脱组成。串联质谱仪使用选定的反应监测器在正电喷雾模式下运行,其转变为m / z 366.15至286.40。血浆中吗啡-3-O-硫酸盐的测量范围是5-500 ng / mL,吗啡-6-O-硫酸盐的测量范围是4.5-454 ng / mL。尿液中,吗啡-3-O-硫酸盐的测量范围为50-5000 ng / mL,吗啡-6-O-硫酸盐的测量范围为45.4-4544 ng / mL。尿液和血浆中的分析物的测定内和总不精密度(变异系数)均低于11%。在真实的尿液和血浆样品中发现了可定量的3-O-硫酸吗啡水平。只有一个真实的尿液样本中含有可检测水平的6-O-吗啡硫酸盐,而血浆样本中没有检测到6-O-吗啡。

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