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Rapid and simple determination of indinavir in serum, urine, and cerebrospinal fluid using high-performance liquid chromatography.

机译:使用高效液相色谱法快速,简单地测定血清,尿液和脑脊髓液中的茚地那韦。

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摘要

A method for analysis of indinavir in serum, cerebrospinal fluid, and urine was developed. The method is based on liquid-liquid extraction followed by high performance liquid chromatography with UV detection. The method has a shorter analysis time than previously published methods, and it is sensitive enough to measure levels in all three fluids under routine clinical conditions. The method is linear up to 32 micromol/L, the limit of detection is 0.01 micromol/L, and recovery of the method is 86%. The interassay coefficient of variation at 2.0 micromol/L was 2.8%, and no internal standard is needed. Over 700 clinical samples have been analyzed by this method, and concomitant antiviral drugs do not interfere with the assay. Paroxetin and dipyridamol are the only two compounds encountered to elute with retention times similar to that of indinavir. Examples of chromatograms and a pharmacokinetic curve are given. The method is well suited for routine therapeutic drug monitoring as well as for pharmacokinetic studies for research purposes.
机译:建立了分析血清,脑脊液和尿液中茚地那韦的方法。该方法基于液-液萃取,然后进行高效液相色谱和紫外检测。该方法的分析时间比以前发表的方法要短,并且灵敏度足以在常规临床条件下测量所有三种液体的水平。该方法线性最高可达32 micromol / L,检出限为0.01 micromol / L,回收率为86%。测定间变异系数在2.0 micromol / L下为2.8%,不需要内标。通过这种方法已经分析了700多个临床样品,并且伴随的抗病毒药物不会干扰测定。帕罗西汀和双嘧达莫是仅有的两个洗脱时间与茚地那韦相似的化合物。给出了色谱图和药代动力学曲线的例子。该方法非常适合常规治疗药物监测以及用于研究目的的药代动力学研究。

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