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机构地区:[1]中国科学技术大学化学系,安徽合肥230026
出 处:《分析测试学报》2007年第z1期30-31,共2页Journal of Instrumental Analysis
基 金:国家自然科学基金资助项目(20332020)
摘 要:A rapid and sensitive liquid chromatography-tandem mass spectrometry method was developed and validated to quantify levonorgestrel in human plasma.After liquid-liquid extraction with ethyl acetate,the analytes were separated on a Phenomenex Luna C18 column interfaced with a tripe-quadrupole tandem mass spectrometer using positive electrospray ionization.Norethindrone was used as the internal standard.The standard calibration curve was linear over the concentration range 0.625-40 ng·mL-1.The intra-day and inter-day precisions were less than 8.16% from the determination of QC samples.Accuracy was within ±7.3%.The method was successfully applied for pharmacokinetic study of levonorgestrel after oral administration of 1.5 mg levonorgestrel to 20 healthy volunteers.A rapid and sensitive liquid chromatography-tandem mass spectrometry method was developed and validated to quantify levonorgestrel in human plasma.After liquid-liquid extraction with ethyl acetate,the analytes were separated on a Phenomenex Luna C18 column interfaced with a tripe-quadrupole tandem mass spectrometer using positive electrospray ionization.Norethindrone was used as the internal standard.The standard calibration curve was linear over the concentration range 0.625-40 ng·mL-1.The intra-day and inter-day precisions were less than 8.16% from the determination of QC samples.Accuracy was within ±7.3%.The method was successfully applied for pharmacokinetic study of levonorgestrel after oral administration of 1.5 mg levonorgestrel to 20 healthy volunteers.
关 键 词:LEVONORGESTREL Human plasmal Liquid chromatographyl Mass spectrometry
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