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通过负离子化学电离质谱法对人血浆中吗啡葡糖醛酸苷进行定量气相色谱/质谱分析。

Quantitative gas chromatographic/mass spectrometric analysis of morphine glucuronides in human plasma by negative ion chemical ionization mass spectrometry.

作者信息

Leis Hans Jörg, Fauler Günter, Raspotnig Günther, Windischhofer Werner

机构信息

University Children's Hospital, Division of Analytical Biochemistry and Mass Spectrometry, Auenbruggerplatz 30, A-8036 Graz, Austria.

出版信息

J Mass Spectrom. 2002 Apr;37(4):395-400. doi: 10.1002/jms.294.

Abstract

A sensitive and specific method for the determination of morphine glucuronides in human plasma is presented. Morphine glucuronides, namely morphine-6-glucuronide (M6G) and morphine-3-glucuronide (M3G), were extracted from plasma by solid-phase extraction on C(18) cartridges at pH 9.3 and derivatized to their pentafluorobenzyl ester trimethylsilyl ether derivatives. The compounds were measured by gas chromatography/negative ion chemical ionization mass spectrometry without any further purification. Using this detection mode, a diagnostic useful fragment ion at m/z 748 was obtained at high relative abundance for both target compounds. [(2)H(3)]-labeled morphine glucuronides were used as internal standards. Calibration graphs were calculated by polynomial fit within a range of 10-1280 and 15-1920 nmol l(-1) for the 6- and 3-glucuronide, respectively. At the limit of quantitation (LOQ), the inter-assay precision was 2.21% (M3G) and 2.23% (M6G) and the GC/MS assay variability was 1.8% (M3G) and 0.9% (M6G). The accuracy at the LOQ showed deviations of +4.92% (M3G) and +1.5% (M6G). The sample recovery after solid-phase extraction was 84.7% for both M3G and M6G. The method is rugged, rapid and robust and has been applied to the batch analysis of morphine glucuronides during pharmacokinetic profiling of the drugs.

摘要

本文介绍了一种灵敏且特异的测定人血浆中吗啡葡萄糖醛酸苷的方法。吗啡葡萄糖醛酸苷,即吗啡 - 6 - 葡萄糖醛酸苷(M6G)和吗啡 - 3 - 葡萄糖醛酸苷(M3G),在pH 9.3条件下通过C(18) 柱固相萃取从血浆中提取,并衍生化为其五氟苄基酯三甲基硅醚衍生物。化合物无需进一步纯化,通过气相色谱/负离子化学电离质谱进行测定。采用这种检测模式,两种目标化合物均在高相对丰度下获得了m/z 748的诊断有用碎片离子。[(2)H(3)]标记的吗啡葡萄糖醛酸苷用作内标。分别在10 - 1280和15 - 1920 nmol l(-1)范围内通过多项式拟合计算6 - 葡萄糖醛酸苷和3 - 葡萄糖醛酸苷的校准曲线。在定量限(LOQ)处,批内精密度分别为2.21%(M3G)和2.23%(M6G),气相色谱/质谱分析的变异系数分别为1.8%(M3G)和0.9%(M6G)。定量限处的准确度偏差分别为 +4.92%(M3G)和 +1.5%(M6G)。固相萃取后的样品回收率对于M3G和M6G均为84.7%。该方法耐用、快速且稳健,已应用于药物药代动力学分析过程中吗啡葡萄糖醛酸苷的批量分析。

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