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生物样品中哌替啶的质谱测定(作者译)

[Mass spectrometric determination of pethidine in biological samples (author's transl)].

作者信息

Ihn W, Schade W, Müller B, Peiker G

出版信息

Pharmazie. 1980;35(10):598-601.

PMID:7454740
Abstract

A mass spectrometric method for the determination of pethidine in nanogram range is described. This method excels by its high sensitivity and specificity, which ensures the reliable quantitative determination of the pharmacon also in complex media. Pethidine is extracted with ether from the respective sample together with its (D5) derivative (which is added as an internal standard) and directly (or after gas-chromatographic separation from other components) determined by mass spectrometry. The pethidine concentration is calculated from the ratio of the sums of the molecular ion intensities M+-pethidine/M+-(D5)-pethidine, which are obtained from the chromatographic column by repetitive scanning during the elution of pethidine and its (D5) derivative, respectively.

摘要

本文描述了一种用于测定纳克级哌替啶的质谱方法。该方法具有高灵敏度和特异性,即使在复杂介质中也能确保对该药物进行可靠的定量测定。哌替啶与其(D5)衍生物(作为内标添加)一起从相应样品中用乙醚萃取,然后直接(或在与其他成分进行气相色谱分离后)通过质谱法测定。哌替啶浓度根据分子离子强度之和的比值M+-哌替啶/M+ -(D5)-哌替啶计算得出,这些强度分别是在哌替啶及其(D5)衍生物洗脱过程中通过对色谱柱进行重复扫描获得的。

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