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0期临床试验中血浆和尿液中NSC 737664(ABT - 888:一种聚(ADP - 核糖)聚合酶(PARP)抑制剂)的液相色谱测定

Liquid Chromatographic Determination of NSC 737664 (ABT-888: an Inhibitor of Poly(ADP-ribose) Polymerase (PARP)) in Plasma and Urine in a Phase 0 Clinical Trial.

作者信息

Phillips Lawrence R, Hill Kimberly D, Majerova Eva

机构信息

Biological Testing Branch, Developmental Therapeutics Program, Division of Cancer Treatment and Diagnosis, National Cancer Institute at Frederick, Frederick, MD 21702.

出版信息

J Liq Chromatogr Relat Technol. 2009 Jan;32(2):261-272. doi: 10.1080/10826070802603351.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e3f/2615403/3e3b2db38d68/nihms60470f1.jpg

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