Laboratory of Drug Metabolism and Pharmacokinetics, Beijing Institute of Radiation Medicine, Beijing 100850, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2010 Jul 1;878(21):1893-8. doi: 10.1016/j.jchromb.2010.05.015. Epub 2010 May 19.
An improved liquid chromatographic method with on-line solid phase extraction (SPE) and tandem mass spectrometric detection was optimised for quantification of the anti-HIV peptide Sifuvirtide in human plasma. The SPE sorbents, loading buffer composition and other aspects of the on-line SPE column were investigated in detail for efficiently extracting the interesting peptides and simultaneously discarding the large amount of proteins. The gradient elution program was optimised on the analysis column to decrease the matrix effect and obtain excellent selectivity. The multiple charge ion at m/z 946.4 of Sifuvirtide was quantified by a linear ion trap mass spectrometer, operating in the positive mode, and selective reaction monitoring (SRM) acquisition. Method validation results demonstrated that the linear calibration curve covered a range of 6.1-6250 ng/mL, and the correlation coefficients (r(2)) were above 0.992. The lower limit of detection (LLOD) with a signal-to-noise (S/N) ratio higher than 10 was 6.1 ng/mL. The accuracy ranged from -7.6 to 10.6%, and the intra- and inter-batch precisions were less than 8.7% and 5.5%, respectively. Finally, more than nine hundred of samples from a clinical trial was completely analyzed using this on-line SPE coupled HPLC-MS/MS system in one single week, due to the rapid run-time of individual sample (6.5 min).
建立了一种固相萃取在线联用高效液相色谱-串联质谱测定人血浆中抗 HIV 肽 Sifuvirtide 的方法。对 SPE 小柱的固相萃取条件、上样缓冲液组成等方面进行了详细的考察,实现了对目的肽的有效提取和对大量蛋白的有效去除。采用梯度洗脱程序对分析柱进行优化,以降低基质效应,获得良好的选择性。采用正离子多电荷离子监测(MRM)方式,对 Sifuvirtide 的母离子 m/z 946.4 定量分析。方法学验证结果表明,该方法在 6.1-6250 ng/mL 范围内线性关系良好,相关系数(r(2))大于 0.992。检测限为 6.1 ng/mL(信噪比大于 10)。准确度在-7.6%至 10.6%之间,日内和日间精密度均小于 8.7%和 5.5%。最终,本方法在一周内完成了 900 多份临床样品的检测,单个样品的分析时间仅为 6.5min,具有快速的特点。