Noble S, Neville D, Houghton R
Quotient Bio Analytical Sciences, Newmarket Road, Fordham, Cambridge CB7 5WW, United Kingdom.
Quotient Bio Analytical Sciences, Newmarket Road, Fordham, Cambridge CB7 5WW, United Kingdom.
J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Feb 1;947-948:173-8. doi: 10.1016/j.jchromb.2013.12.028. Epub 2013 Dec 30.
A rapid, simple and sensitive method was developed for the determination of 8-iso-PGF2α in urine using ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS); 8-iso-PGF2α-d4 was used as the internal standard (IS). Chromatographic separation was performed using an Acquity BEH C18 column with a mobile phase composition of A: 0.1% acetic acid in methanol:acetonitrile (1:1, v:v) and B: 0.1% acetic acid in water (A:B, 32.5:67.5, v:v). Detection was performed on a triple-quadrupole tandem mass spectrometer using atmospheric pressure chemical ionization (APCI) in negative mode and using multiple reaction monitoring (MRM). The MS/MS ion transitions monitored were m/z 353→193 and 357→197 for 8-iso-PGF2α and IS, respectively. The calibration curve was prepared in PBS buffer because of the presence of endogenous concentrations of analyte in the control matrix; the internal standard successfully correcting for matrix effects. Good linearity was observed over the concentration range of 0.025-20 ng/mL; the method proving to be accurate and reliable was successfully used in support of a pharmacodynamic study in humans.
建立了一种快速、简便且灵敏的超高效液相色谱串联质谱法(UPLC-MS/MS)测定尿液中8-异前列腺素F2α(8-iso-PGF2α);以8-异前列腺素F2α-d4作为内标(IS)。采用Acquity BEH C18色谱柱进行色谱分离,流动相组成为A:甲醇:乙腈(1:1,v:v)中含0.1%乙酸,B:水中含0.1%乙酸(A:B,32.5:67.5,v:v)。在三重四极杆串联质谱仪上采用大气压化学电离(APCI)负离子模式和多反应监测(MRM)进行检测。监测的8-iso-PGF2α和内标的MS/MS离子跃迁分别为m/z 353→193和357→197。由于对照基质中存在内源性分析物浓度,在磷酸盐缓冲盐溶液(PBS)中制备校准曲线;内标成功校正了基质效应。在0.025 - 20 ng/mL浓度范围内观察到良好的线性;该方法被证明准确可靠,成功用于支持一项人体药效学研究。