Ebeid Kareem, Ho Giang N, Salem Aliasger K
Division of Pharmaceutics and Translational Therapeutics, College of Pharmacy, University of Iowa, Iowa City, IA 51141, USA.
Division of Pharmaceutics and Translational Therapeutics, College of Pharmacy, University of Iowa, Iowa City, IA 51141, USA.
J Chromatogr B Analyt Technol Biomed Life Sci. 2017 Feb 15;1044-1045:70-76. doi: 10.1016/j.jchromb.2016.12.031. Epub 2016 Dec 30.
A sensitive and precise method is described for the simultaneous determination of two small molecule kinase inhibitors: MK-1775 (MK) and AZD-7762 (AZD), in acetonitrile (ACN)-aqueous solution and in mouse plasma. A Nova-Pak C18 reversed phase column (3.9mm×150mm, 4μm, 60Å) was utilized in the separation using an isocratic mobile phase of 0.1% v/v triethylamine in phosphate buffer (pH=7.4): acetonitrile (ACN) (60:40, v/v), at a flow rate of 0.8mL/min. Detection wavelength was set at 310nm for both MK and AZD, and 431nm for the internal standard sunitinib (SUN). The developed method was validated following the ICH guidelines and it was shown to be accurate, precise and linear in the range of 41ng/mL to 8333ng/mL for both drugs in the ACN-aqueous solution and from 83ng/mL to 8333ng/mL for both drugs in mouse plasma samples. For the first time, the presented data suggest the suitability of this method for the simultaneous separation and quantification of MK and AZD in both ACN aqueous solution as well as in mouse plasma samples.
本文描述了一种灵敏且精确的方法,用于同时测定乙腈(ACN)-水溶液和小鼠血浆中的两种小分子激酶抑制剂:MK-1775(MK)和AZD-7762(AZD)。采用Nova-Pak C18反相柱(3.9mm×150mm,4μm,60Å)进行分离,流动相为磷酸盐缓冲液(pH = 7.4)中0.1% v/v三乙胺与乙腈(ACN)(60:40,v/v)的等度洗脱液,流速为0.8mL/min。MK和AZD的检测波长均设定为310nm,内标舒尼替尼(SUN)的检测波长设定为431nm。所建立的方法按照ICH指南进行了验证,结果表明在ACN-水溶液中两种药物的线性范围为41ng/mL至8333ng/mL,在小鼠血浆样品中两种药物的线性范围为83ng/mL至8333ng/mL,该方法准确、精密。首次有数据表明该方法适用于同时分离和定量ACN水溶液以及小鼠血浆样品中的MK和AZD。