Licea-Perez Hermes, Wang Sherry, Bowen Chester L, Yang Eric
Worldwide Bioanalysis, Drug Metabolism and Pharmacokinetics, GlaxoSmithKline Pharmaceuticals, 709 Swedeland Road, King of Prussia, PA 19406, USA.
J Chromatogr B Analyt Technol Biomed Life Sci. 2007 Jun 1;852(1-2):69-76. doi: 10.1016/j.jchromb.2006.12.052. Epub 2007 Jan 13.
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 microL plasma, the methods were validated over the concentration ranges of 0.01-2 ng/mL and 0.1-20 ng/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 (> or =500 microL), 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.
开发了两种使用超高效液相色谱-串联质谱联用(UPLC-MS/MS)的半自动、相对高通量方法,用于同时测定人血浆中炔雌醇(EE)与19-炔诺酮(NE)或左炔诺孕酮(LN)的组合。使用300微升血浆,分别在0.01-2 ng/mL和0.1-20 ng/mL的浓度范围内对EE和NE(或LN)的方法进行了验证。现有的人血浆中口服避孕药的测定方法需要大量血浆(≥500微升),且样品提取劳动强度大。液相色谱运行时间至少为6分钟,每天只能分析约100个样品。在本工作中,通过采用半自动样品制备过程,包括液-液萃取和用丹磺酰氯衍生化,然后在小粒径柱上进行UPLC分离,运行时间达到2.7分钟,大大提高了通量。验证和实际样品分析结果表明,这两种方法都耐用、精密、准确,非常适合支持药代动力学研究,一天内可提取和分析约300个样品。