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 >Development and validation of a LC-MS/MS method with electrospray ionization for determination of LASSBio-579 in rat plasma.
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Development and validation of a LC-MS/MS method with electrospray ionization for determination of LASSBio-579 in rat plasma.

机译:LC-MS / MS方法的开发和验证,该方法用于测定大鼠血浆中LASSBio-579的电喷雾电离。

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摘要

A simple and sensitive LC-MS/MS analytical method was developed and validated for the determination of LASSBio-579 in plasma rat, using fluconazole as internal standard. Analyses were performed on a Shimadzu HPLC system using a Shimadzu C18 column and isocratic elution with acetonitrile-water (80:20, v/v), containing 0.4mM ammonium hydroxide and 0.2 mM acetic acid at a flow rate of 1.0 ml/min (split ratio 1:5). A Micromass triple quadrupole mass spectrometer, equipped with an electrospray ionization interface, operated in the positive mode. Plasma samples were deproteinized with acetonitrile (1:2) and 50 microl of the supernatant were injected into the system. The retention times of LASSBio-579 and IS were approximately 4.7 and 2.4 min, respectively. Calibration curves in spiked plasma were linear over the concentration range of 30-2000 ng/ml with determination coefficient >0.98. The lower limit of quantification was 30 ng/ml. The accuracy of method was within 15%. Intra- and inter-day relative standard deviations were less or equal to 13.5% and 6.4%, respectively. The applicability of the LC-MS/MS method for pharmacokinetic studies was tested using plasma samples obtained after intraperitoneal administration of LASSBio-579 to male Wistar rats. No interference from endogenous substances was observed, showing the specificity of the method developed. The reported method can provide the necessary sensitivity, linearity, precision, accuracy, and specificity to allow the determination of LASSBio-579 in pre-clinical pharmacokinetic studies.
机译:以氟康唑为内标,开发了一种简单而灵敏的LC-MS / MS分析方法,并已用于测定血浆大鼠中LASSBio-579的有效性。使用Shimadzu C18色谱柱在Shimadzu HPLC系统上进行分析,并使用乙腈-水(80:20,v / v)进行等度洗脱,该乙腈水含有0.4mM氢氧化铵和0.2 mM乙酸,流速为1.0 ml / min(分配比例为1:5)。配备电喷雾电离界面的Micromass三重四极杆质谱仪以正模式运行。血浆样品用乙腈(1:2)脱蛋白,并将50微升上清液注入系统。 LASSBio-579和IS的保留时间分别约为4.7和2.4分钟。加标血浆中的校准曲线在30-2000 ng / ml的浓度范围内呈线性,测定系数> 0.98。定量的下限为30 ng / ml。方法的准确度在15%以内。日内和日间相对标准偏差分别小于或等于13.5%和6.4%。使用LASSBio-579腹腔注射给雄性Wistar大鼠后获得的血浆样品,测试了LC-MS / MS方法在药代动力学研究中的适用性。没有观察到来自内源性物质的干扰,表明了所开发方法的特异性。报告的方法可以提供必要的灵敏度,线性,精密度,准确性和特异性,以便在临床前药代动力学研究中确定LASSBio-579。

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