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首页> 外文期刊>Bioanalysis >Quantification of total and unbound concentrations of lorazepam, oxazepam and temazepam in human plasma by ultrafiltration and LC-MS/MS.
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Quantification of total and unbound concentrations of lorazepam, oxazepam and temazepam in human plasma by ultrafiltration and LC-MS/MS.

机译:通过超滤和LC-MS / MS定量测定人血浆中劳拉西m,奥沙西m和替马西m的总和未结合浓度。

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BACKGROUND: A fast and sensitive assay for quantifying total and unbound concentrations of lorazepam (Lzp), oxazepam (Ozp) and temazepam (Tzp) in human plasma was needed for a plasma protein binding study. RESULTS: Plasma samples were precipitated with acetonitrile for determination of total concentrations or subjected to ultrafiltration for determination of unbound concentrations. An LC-MS/MS assay was developed with an Allure(R) PFP propyl column and a mobile phase of 35% acetonitrile/0.1% formic acid over 4.5 min and ESI+-MS/MS detection. Matrix effects were negligible in plasma and approximately 70% in ultrafiltrate but were accounted for by the internal standards Lzp-d, Ozp-d and Tzp-d. The assay was validated for total concentrations of 10-100 ng/ml Lzp, 200-2000 ng/ml Ozp and 100-1000 ng/ml Tzp, and for unbound concentrations of 1-10 ng/ml Lzp, 20-200 ng/ml Ozp and 10-100 ng/ml Tzp. Precision was <14% CV and accuracy was 96-110% throughout the calibration range. The mean precision of triplicate analysis of 60 study samples was <4% CV for total and <8% CV for unbound concentrations. CONCLUSION: A fast and sensitive assay was developed and validated. It has been applied successfully to a protein binding study.
机译:背景:血浆蛋白结合研究需要一种快速灵敏的测定方法,用于定量测定人血浆中劳拉西m(Lzp),奥沙西m(Ozp)和替马西m(Tzp)的总和未结合浓度。结果:血浆样品用乙腈沉淀以测定总浓度,或进行超滤以测定未结合浓度。用AllurePFP丙基柱和在4.5分钟内通过35%乙腈/0.1%甲酸的流动相和ESI + -MS / MS检测开发了LC-MS / MS测定法。血浆中的基质效应可忽略不计,超滤液中的基质效应可忽略不计,但内标Lzp-d,Ozp-d和Tzp-d可以解释。验证了该测定法的总浓度为10-100 ng / ml Lzp,200-2000 ng / ml Ozp和100-1000 ng / ml Tzp,未结合浓度为1-10 ng / ml Lzp,20-200 ng / ml ml Ozp和10-100 ng / ml Tzp。在整个校准范围内,精度为<14%CV,精度为96-110%。 60个研究样品的三次重复分析的平均精度分别为:总量的<4%CV和未结合浓度的<8%CV。结论:开发并验证了一种快速灵敏的测定方法。它已成功应用于蛋白质结合研究。

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