Leis H J, Windischhofer W, Fauler G
University Children's Hospital, Division of Analytical Biochemistry and Mass Spectrometry, Auenbruggerplatz 30, A-8036 Graz, Austria.
Rapid Commun Mass Spectrom. 2002;16(7):646-9. doi: 10.1002/rcm.618.
A sensitive and specific method for the quantitative determination of morphine in human plasma is presented. Morphine was extracted from plasma by solid phase extraction on C18 and converted to its pentafluorobenzyl carbonate trimethylsilyl derivative. The derivatives were analysed without further purification. Using gas chromatography/negative ion chemical ionisation mass spectrometry, a useful diagnostic fragment ion at m/z 356 is obtained at high relative abundance. Deuterated morphine was used as internal standard. Calibration graphs were linear within the range 1.25 to 320 nmol/L. Intra-day precision was 3.82% (15 nmol/L), 2.85% (75 nmol/L) and 4.13% (225 nmol/L), inter-day variability was found to be 1.77% (15 nmol/L), 4.95% (75 nmol/L) and 9.88% (225 nmol/L). Inter-day accuracy showed deviations of 2.18% (15 nmol/L), -0.72% (75 nmol/L) and -0.13% (225 nmol/L). The method is rugged and robust and has been applied to the batch analysis of morphine during pharmacokinetic profiling of the drug.
本文介绍了一种灵敏且特异的定量测定人血浆中吗啡的方法。吗啡通过在C18上进行固相萃取从血浆中提取出来,并转化为其五氟苄基碳酸酯三甲基硅烷基衍生物。衍生物无需进一步纯化即可进行分析。使用气相色谱/负离子化学电离质谱法,可获得相对丰度较高的质荷比为356的有用诊断碎片离子。氘代吗啡用作内标。校准曲线在1.25至320 nmol/L范围内呈线性。日内精密度分别为3.82%(15 nmol/L)、2.85%(75 nmol/L)和4.13%(225 nmol/L),日间变异分别为1.77%(15 nmol/L)、4.95%(75 nmol/L)和9.88%(225 nmol/L)。日间准确度偏差分别为2.18%(15 nmol/L)、-0.72%(75 nmol/L)和-0.13%(225 nmol/L)。该方法耐用且稳健,已应用于该药物药代动力学分析过程中吗啡的批量分析。