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采用气相色谱-负离子化学电离质谱法测定人或犬血浆中乙酰曲前列尼尔及其代谢物曲前列尼尔。

Determination of acetyltrimoprostil and its metabolite trimoprostil in human or dog plasma by gas chromatography-negative-ion chemical ionization mass spectrometry.

作者信息

Rubio F, Garland W A

出版信息

J Chromatogr. 1985 May 3;339(2):313-20. doi: 10.1016/s0378-4347(00)84658-7.

Abstract

A sensitive and specific procedure is described for the determination of the antisecretory prostaglandin acetyltrimoprostil and its metabolite trimoprostil in human or dog plasma using gas chromatography--negative-ion chemical ionization mass spectrometry (GC--NICI-MS). Trideuterated analogues of both compounds are added to plasma as the internal standards. The plasma is extracted at pH 7.3 with benzene--dichloromethane (9:1), and the residue of the organic extract is reacted at room temperature with pentafluorobenzyl bromide in the presence of 18-crown-6-ether and potassium acetate. The derivatives are reconstituted in heptane, and appropriate aliquots are analyzed by GC--NICI-MS with selected-ion monitoring of the intense (M--C6F5CH2)- fragment ions of acetyltrimoprostil (m/z 419), trimoprostil (m/z 377), and their respective trideuterated analogues (m/z 422 and m/z 380, respectively). Quantitation of an experimental plasma sample is based on a comparison of the m/z 419 versus m/z 422 and m/z 377 versus m/z 380 ion ratios in each sample to that obtained from the analysis of drug-free plasma fortified with various amounts of both protio compounds, and a fixed amount of each trideuterated internal standard. The limit of quantitation of the assay for human plasma is 0.2 ng ml-1 with mean relative standard deviations at this concentration of 15.5% and 9.7% for acetyltrimoprostil and trimoprostil, respectively.

摘要

描述了一种灵敏且特异的方法,用于使用气相色谱-负离子化学电离质谱法(GC-NICI-MS)测定人或犬血浆中的抗分泌前列腺素乙酰曲莫前列素及其代谢物曲莫前列素。将这两种化合物的氘代类似物作为内标添加到血浆中。血浆在pH 7.3下用苯-二氯甲烷(9:1)萃取,有机萃取物的残留物在室温下与五氟苄基溴在18-冠-6-醚和乙酸钾存在下反应。衍生物用庚烷复溶,取适当的等分试样通过GC-NICI-MS进行分析,对乙酰曲莫前列素(m/z 419)、曲莫前列素(m/z 377)及其各自的氘代类似物(分别为m/z 422和m/z 380)的强(M-C6F5CH2)-碎片离子进行选择离子监测。实验血浆样品的定量基于比较每个样品中m/z 419与m/z 422以及m/z 377与m/z 380的离子比率与用各种量的原化合物和固定量的每种氘代内标强化的无药血浆分析所获得的比率。该方法对人血浆的定量限为0.2 ng/ml,在此浓度下,乙酰曲莫前列素和曲莫前列素的平均相对标准偏差分别为15.5%和9.7%。

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