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首页> 外文期刊>British Journal of Pharmaceutical Research >High Throughput Lc-Ms/Ms Method for the Quantitation of Emtricitabine in Human Plasma by Solid Phase Extraction Using 96 Well Plate Format
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High Throughput Lc-Ms/Ms Method for the Quantitation of Emtricitabine in Human Plasma by Solid Phase Extraction Using 96 Well Plate Format

机译:高通量LC-MS / MS方法通过96孔板格式固相萃取定量测定人血浆中的恩曲他滨

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Aim: To develop and validate sensitive, high-throughput Liquid chromatography–mass spectrometry method for the quanti?cation of Emtricitabine in human plasma using Lamivudine as an internal standard (ISTD) using 96 well plate format solid phase extraction (SPE) technique. Methodology: The samples were extracted from plasma using solid phase extraction (SPE) in 96 well plate format. After extraction the analyte and internal standard were analyzed on Inertsil ODS column with dimensions 4.6 X 100 mm, 5 μm using a mobile phase consisting of Methanol: 0.2% formic acid in water 85:15, v/v. The precursor and product ions of the analytes were monitored on a triple quadrupole instrument operated in the positive ionization mode. Results: The method was validated with concentration range of 5.024 to 5023.725 ng/mL. The relative recoveries were ranging from 60.7 to 65.9%. Three validation batches were performed with five QC levels (LLOQ, LQC, MQC II, MQC and HQC). Across three validation runs the inter batch precision (%CV) was ≤ 9.2% and the accuracy was between 98.9–106.0%. All the stability experiments found satisfactory. Conclusion: According to the method validation results, the current method was found to be specific, accurate, sensitive, precise and high throughput method. This method can be used for the estimation of Emtricitabine in human plasma during routine analysis.
机译:目的:建立和验证灵敏的高通量液相色谱-质谱法,以拉米夫定为内标(ISTD),采用96孔板格式固相萃取(SPE)技术定量测定人血浆中的恩曲他滨。方法:采用固相萃取(SPE)以96孔板形式从血浆中萃取样品。提取后,使用流动相由甲醇:0.2%甲酸的水溶液(体积比为85:15)在Inertsil ODS色谱柱上分析尺寸为4.6 X 100 mm,5μm的分析物和内标。分析物的前体离子和产物离子在以正电离模式运行的三重四极杆仪器上进行监测。结果:该方法在5.024至5023.725 ng / mL的浓度范围内得到验证。相对回收率在60.7%至65.9%之间。使用五个QC级别(LLOQ,LQC,MQC II,MQC和HQC)执行了三个验证批次。在三个验证运行中,批间精度(%CV)≤9.2%,精度在98.9-106.0%之间。所有稳定性实验均令人满意。结论:根据方法验证结果,发现当前方法是一种特异,准确,灵敏,精确和高通量的方法。该方法可用于常规分析过程中人体血浆中恩曲他滨的估计。

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