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Analysis of ritonavir in plasma/serum and tissues by high-performance liquid chromatography.

机译:高效液相色谱法分析血浆/血清和组织中的ritonavir。

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摘要

A method has been developed to quantify ritonavir concentrations in human plasma and in mouse serum, liver, and brain using high-performance liquid chromatography. Extraction recoveries for ritonavir and its internal standard averaged greater than 95%. Within-day variability, expressed as a coefficient of variation, averaged 6% over the concentration range 0.5 microg/mL to 15 microg/mL ritonavir, and between-day variability averaged 5.6% over 5 microg/mL to 15 microg/mL ritonavir. The method was applied to quantitation of ritonavir in mouse serum and tissue. Measured values deviated less than 5% from the actual values in mouse serum, liver, and brain samples containing 5 microg/mL ritonavir. The slopes of calibration curves for extracted calf serum, mouse serum, mouse liver and mouse brain standards were nearly identical to the calibration slope of standards which were not extracted. All curves were linear through zero, and r2 was no less than 0.998 for any form of calibration. In addition, there was no chromatographic interference from commonly prescribed medications.
机译:已经开发了一种方法以使用高效液相色谱法量化人血浆和小鼠血清,肝脏和脑中的Ritonavir浓度。提取Ritonavir及其内标平均值的萃取回收率大于95%。在日内变异性,表示为变异系数,在浓度范围内平均为0.5微孔/ ml至15μg/ ml ritonavir,并且在日间变异平均为5.6%超过5微孔/ mL至15μg/ ml ritonavir。该方法应用于小鼠血清和组织中Ritonavir的定量。测量值偏离含有5μg/ mL ritonavir的小鼠血清,肝脏和脑样品中的实际值小于5%。提取的小牛血清,小鼠血清,小鼠肝脏和小鼠脑标准校准曲线的斜率几乎与未提取的标准标准的校准斜率几乎相同。对于任何形式的校准,所有曲线都是线性的,通过零,R2不小于0.998。此外,普通规定的药物没有色谱干扰。

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