首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Validated bioanalytical method for the quantification of RGB-286638, a novel multi-targeted protein kinase inhibitor, in human plasma and urine by liquid chromatography/tandem triple-quadrupole mass spectrometry.
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Validated bioanalytical method for the quantification of RGB-286638, a novel multi-targeted protein kinase inhibitor, in human plasma and urine by liquid chromatography/tandem triple-quadrupole mass spectrometry.

机译:通过液相色谱/串联三重四极杆质谱法在人血浆和尿液中定量的新型多靶点蛋白激酶抑制剂RGB-286638的有效生物分析方法。

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摘要

A rapid and sensitive liquid chromatography/tandem mass spectrometry (LC-MS/MS) method has been developed and validated for the quantitative determination of RBG-286638, a novel multi-targeted protein kinase inhibitor, in 200 microl aliquots of human potassium EDTA plasma with deuterated RGB-286638 as internal standard. The sample extraction and cleaning-up involved a simple liquid-liquid extraction with 100 microl aliquots of acetonitrile and 1 ml aliquots of n-butylchloride. Urine was accurately 5- and 10-fold diluted in blank plasma prior to extraction. Chromatographic separations were achieved on a reversed phase C18 column eluted at a flow-rate of 0.250 ml/min on a gradient of 0.2 mM ammonium formate and acetonitrile both acidified with 0.1% formic acid. The overall cycle time of the method was 7 min, with RGB-286638 eluting at 1.9 min. The multiple reaction monitoring transitions were set at 546>402 (m/z), and 549>402 (m/z) for RGB-286638 and the internal standard, respectively. The calibration curves were linear over the range of 2.00 to 1000 ng/ml with the lower limit of quantitation validated at 2.00 ng/ml. The within-run and between-run precisions were within 7.90%, while the accuracy ranged from 92.2% to 99.7%. The method was successfully applied to samples derived from a clinical study.
机译:已经开发了一种快速灵敏的液相色谱/串联质谱(LC-MS / MS)方法,并已用于定量测定200微升人EDTA钾血浆中的新型多靶点蛋白激酶抑制剂RBG-286638以氘代RGB-286638作为内标。样品的提取和净化涉及到简单的液-液萃取,其中包括100微升乙腈等分试样和1毫升正丁基氯的等分试样。提取前,尿液在空白血浆中准确稀释了5倍和10倍。在反相C18柱上进行色谱分离,以0.250 ml / min的流速在0.2 mM甲酸铵和乙腈的梯度下洗脱,两者均用0.1%甲酸酸化。该方法的总循环时间为7分钟,其中RGB-286638洗脱时间为1.9分钟。对于RGB-286638和内标,多重反应监控转换分别设置为546> 402(m / z)和549> 402(m / z)。校准曲线在2.00至1000 ng / ml的范围内呈线性,定量的下限确认为2.00 ng / ml。批内和批间精度在7.90%以内,而精度范围为92.2%至99.7%。该方法已成功应用于源自临床研究的样品。

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