...
首页> 外文期刊>The Journal of automatic chemistry >A Validated Volumetric Absorptive Microsampling-Liquid Chromatography Tandem Mass Spectrometry Method to Quantify Doxycycline Levels in Urine: An Application to Monitor the Malaria Chemoprophylaxis Compliance
【24h】

A Validated Volumetric Absorptive Microsampling-Liquid Chromatography Tandem Mass Spectrometry Method to Quantify Doxycycline Levels in Urine: An Application to Monitor the Malaria Chemoprophylaxis Compliance

机译:经过验证的体积吸收微采样 - 液相色谱串联质谱法,以量化尿液中的毒素水平:施用疟疾嗜症症的合规性

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Because of logistics and cost constraints, monitoring of the compliance to antimalarial chemoprophylaxis by the quantitation of drugs in biological samples is not a simple operation on the field. Indeed, analytical devices are fragile to transport and must be used in a perfectly controlled environment. This is also the case for reagents and supplies, and the waste management is constraining. Thus, samples should be repatriated. They should be frozen after collection and transported with no rupture in the cold chain. This is crucial to generate available and interpretable data but often without any difficulties. Hence, to propose an alternative solution easier to implement, a quantitation method of determining doxycycline in urine has been validated using a volumetric absorptive microsampling (VAMS~(?)) device. As blotting paper, the device is dried after collection and transferred at room temperature, but contrarily to dried spot, the collection volume is perfectly repeatable. Analysis of VAMS~(?) was performed with a high-performance liquid chromatography coupled to a mass spectrometer. The chromatographic separation was achieved on a core-shell C18 column. The mean extraction recovery was 109% (mean RSD, 5.4%, n ?=?6) for doxycycline and 102% (mean RSD, 7.0%) for the internal standard. No matrix effect has been shown. Within-run as within-day precision and accuracy were, respectively, below 14% and ranged from 96 to 106%. The signal/concentration ratio was studied in the 0.25–50? μ g/mL range, and recoveries from back-calculated concentrations were in the 96–105% range (RSD?
机译:由于物流和成本限制,通过在生物样品中定量药物的药物对抗疟嗜嗜症脑化学基因的依从性监测不是对该领域的简单操作。实际上,分析装置易碎到运输,必须在完美控制的环境中使用。这也是试剂和用品的情况,废物管理是约束。因此,样品应该被遣返。在收集后应该冷冻并在冷链中运输并没有破裂。这对于生成可用和可解释的数据来说至关重要,但通常没有任何困难。因此,为了提出更容易实现的替代解决方案,使用体积吸收微内采样(VAMS〜(α))装置验证了确定尿液中尿液中的尿红素的定量方法。作为印迹纸,将器件干燥后在收集后并在室温下转移,但与干燥点相反,收集体积是完全可重复的。通过偶联至质谱仪进行高效液相色谱法进行VAMS〜(α)的分析。在核心壳C18柱上实现了色谱分离。平均提取回收率为109%(平均RSD,5.4%,N?6),用于元环素,102%(平均RSD,7.0%)用于内标。没有显示矩阵效应。随着日期的精确度和精度,分别为14%,范围为96至106%。在0.25-50中研究了信号/浓度比?从后计算浓度的μg/ ml范围和回收率在96-105%范围内(RSD?11.0%)。斜坡上的RSD为10%。为了实现验证,将这种新的定量方法应用于真实样品。并行地,在简单稀释后直接分析样品。没有观察到统计差异,确认使用VAMS〜(?)是监测十氧环素依从性的优秀替代装置。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号