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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >A semi-automated 96-well plate method for the simultaneous determination of oral contraceptives concentrations in human plasma using ultra performance liquid chromatography coupled with tandem mass spectrometry
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A semi-automated 96-well plate method for the simultaneous determination of oral contraceptives concentrations in human plasma using ultra performance liquid chromatography coupled with tandem mass spectrometry

机译:半自动96孔平板法,采用高效液相色谱-串联质谱同时测定人血浆中口服避孕药的浓度

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摘要

Two semi-automated, relatively high throughput methods using ultra performance liquid chromatography coupled with tandem mass spectrometry (UPLC-MS/MS) were developed for the simultaneous determination of ethinyl estradiol (EE) in combination with either 19-norethindrone (NE) or levonorgestrel (LN) in human plasma. Using 300 mu L plasma, the methods were validated over the concentration ranges of 0.01-2 ng/mL and 0.1-20ng/mL for EE and NE (or LN), respectively. The existing methods for the determination of the oral contraceptives in human plasma require large volumes of plasma (>= 500 mu L), and sample extraction is labor-intensive. The LC run time is at least 6 min, enabling analysis of only about 100 samples a day. In the present work the throughput was greatly improved by employing a semi-automated sample preparation process involving liquid-liquid extraction and derivatization with dansyl chloride followed by UPLC separation on a small particle size column achieving a run time of 2.7 min. The validation and actual sample analysis results show that both methods are rugged, precise, accurate, and well suitable to support pharmacokinetic studies where approximately 300 samples can be extracted and analyzed in a day. (c) 2007 Elsevier B.V. All rights reserved.
机译:开发了两种使用超高效液相色谱和串联质谱(UPLC-MS / MS)的半自动化,相对高通量方法,与19-炔诺酮(NE)或左炔诺孕酮同时测定乙炔雌二醇(EE) (LN)在人血浆中。使用300μL血浆,分别在EE和NE(或LN)的0.01-2 ng / mL和0.1-20ng / mL的浓度范围内验证了该方法。用于测定人血浆中口服避孕药的现有方法需要大量血浆(> = 500μL),并且样品提取费时费力。液相色谱运行时间至少为6分钟,每天仅能分析约100个样品。在本工作中,通过采用半自动化的样品制备方法(包括液-液萃取和丹磺酰氯衍生化),然后在小粒径色谱柱上进行UPLC分离,可大大提高通量,从而实现了2.7分钟的运行时间。验证和实际样品分析结果表明,这两种方法均坚固耐用,精确,准确,非常适合支持药代动力学研究,一天可提取和分析约300个样品。 (c)2007 Elsevier B.V.保留所有权利。

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