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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Measurement of ribavirin and evaluation of its stability in human plasma by high-performance liquid chromatography with UV detection
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Measurement of ribavirin and evaluation of its stability in human plasma by high-performance liquid chromatography with UV detection

机译:高效液相色谱-紫外检测技术测定利巴韦林及其在人血浆中的稳定性

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A simple high-performance liquid chromatography method for the determination of the antiviral agent ribavirin in human plasma was developed and validated. The method involved solid-phase extraction on phenyl boronic acid cartridges, a reversed-phase liquid chromatography with a Waters Atlantis dC 18 (150 mm x 3.9 mm, 5 mu m) column and a mobile phase consisting of 10 mM potassium phosphate buffer (pH 4.0), and ultraviolet detection at 207 nm. This assay proved to be sensitive (lower limit of quantification of 0.05 mu g/ml), linear (correlation coefficients >= 0.997), specific (no interference with various potentially co-administrated drugs), reproducible (both intra-day and inter-day coefficients of variation <= 4.3%), and accurate (deviations ranged from -5.6 to 2.2% and from -6.0 to 4.0% for intra-day and inter-day analysis, respectively). The method was applied to therapeutic monitoring of patients undergoing ribavirin treatment for hepatitis C and proved to be robust and reliable. Thus, this method provides a simple, sensitive, precise and reproducible assay for dosing ribavirin that can be readily adaptable to routine use by clinical laboratories with standard equipment. In addition, we evaluated the stability of ribavirin in plasma under various conditions, since no detailed study on thermal stability of ribavirin has been reported so far and discrepant data do exist on ribavirin stability upon conditions that clinical samples commonly experience. Ribavirin was stable in human plasma stored at room temperature for at least 24 h or at -20 degrees C for up to I month, after three freeze-thaw cycles, as well as in samples undergoing heat inactivation of infectious viruses for 60 min at 60 degrees C. The drug was also stable in processed samples stored at -20 degrees C for 3 days (as dried extracts) or at 20 degrees C for 4 days (as reconstituted samples). (C) 2007 Elsevier B.V. All rights reserved.
机译:建立并验证了一种简单高效液相色谱法测定人血浆中抗病毒药利巴韦林的方法。该方法包括在苯基硼酸柱上进行固相萃取,使用Waters Atlantis dC 18(150 mm x 3.9 mm,5μm)色谱柱的反相液相色谱法以及由10 mM磷酸钾缓冲液(pH 4.0)和207 nm的紫外线检测。该检测方法被证明是灵敏的(定量下限为0.05μg / ml),线性的(相关系数> = 0.997),特异性的(对各种潜在的共同给药药物没有干扰),可重复的(当日和每日两次)日变异系数<= 4.3%)和准确度(日内和日间分析的偏差范围分别为-5.6至2.2%和-6.0至4.0%)。该方法已应用于接受病毒唑治疗丙型肝炎的患者的治疗监测,并被证明是可靠且可靠的。因此,该方法提供了简单,灵敏,精确和可重现的利巴韦林剂量测定方法,该方法可以很容易地适应于临床实验室使用标准设备进行常规使用。另外,我们评估了利巴韦林在各种条件下在血浆中的稳定性,因为到目前为止尚未报道有关利巴韦林热稳定性的详细研究,并且在临床样品通常遇到的条件下确实存在有关利巴韦林稳定性的差异数据。在三个冻融循环后,利巴韦林在室温下至少在室温下储存至少24 h或在-20摄氏度下可保存长达1个月的人血浆中稳定,并且在60℃对感染病毒进行热灭活60分钟的样品中,利巴韦林稳定在-20℃下保存3天(作为干燥提取物)或在20℃下保存4天(作为复原样品)的加工样品中,该药物也是稳定的。 (C)2007 Elsevier B.V.保留所有权利。

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