Phillips Lawrence R, Hill Kimberly D, Majerova Eva
Biological Testing Branch, Developmental Therapeutics Program, Division of Cancer Treatment and Diagnosis, National Cancer Institute at Frederick, Frederick, MD 21702.
J Liq Chromatogr Relat Technol. 2009 Jan;32(2):261-272. doi: 10.1080/10826070802603351.
A gradient reversed-phase high performance liquid chromatographic method was developed for determining NSC 737664 (2-[(2R)-2-methylpyrrolidin-2-yl]-1H-benzimidazole-4-carboxamide; ABT-888) in human plasma and urine. Chromatographic separation used a mobile phase composed of 0.1% formic acid in water and 0.1% formic acid in acetonitrile, and a C18 column (150 mm × 4.6 mm, 5µ). Quantitation was performed using UV detection at 300 nm. Chromatographic peak identity was confirmed using positive-ion electrospray ionization mass spectrometry. The method was shown to be specific, accurate and reproducible, and thereby appropriate for monitoring plasma and urine levels of the agent in support of a phase 0 clinical study.
建立了一种梯度反相高效液相色谱法,用于测定人血浆和尿液中的NSC 737664(2-[(2R)-2-甲基吡咯烷-2-基]-1H-苯并咪唑-4-甲酰胺;ABT-888)。色谱分离采用由水中0.1%甲酸和乙腈中0.1%甲酸组成的流动相,以及C18柱(150 mm×4.6 mm,5µ)。使用300 nm处的紫外检测进行定量。使用正离子电喷雾电离质谱法确认色谱峰的同一性。该方法被证明具有特异性、准确性和可重复性,因此适用于监测该药物的血浆和尿液水平,以支持0期临床研究。