...
首页> 外文期刊>Journal of AOAC International >Determination of Polycyclic Aromatic Hydrocarbons in Commercial Parenteral Formulations and Medications Using High-Performance Liquid Chromatography with Diode Array Detection
【24h】

Determination of Polycyclic Aromatic Hydrocarbons in Commercial Parenteral Formulations and Medications Using High-Performance Liquid Chromatography with Diode Array Detection

机译:二极管阵列检测使用高效液相色谱法测定商业肠胃外制剂中多环芳烃和药物的测定

获取原文
获取原文并翻译 | 示例
           

摘要

HPLC coupled to UV diode array detection (DAD) is proposed for the determination of polycyclic aromatic hydrocarbons (PAHs) in pharmaceutical products for parenteral administration. Because rubber is a possible source of PAHs for these products, samples stored in containers with rubber parts were selected for the analysis. The basis for method optimization was EPA Method 8310, which determines 16 priority PAHs in ground water and wastewater by HPLC using both UV and fluorescence detection. Using DAD, two channels were selected for detection, with one operating at 254 nm for the detection of nine PAHs and the other at 225 nm for the detection of seven PAHs. This method allowed for the detection of PAHs using external calibration with LODs and LOQs ranging from 0.001 to 0.060 mu g/mL and from 0.003 to 0.167 mu g/mL, respectively. Within -day precision, expressed as RSD, varied from 1.24 to 7.76% for PAH concentrations from 0.05 to 0.50 mu g/mL, and intraday precision varied from 3.10 to 9.40% for the same concentration range. Method accuracy was confirmed by recoveries of 75-120% of the spiked samples. This method was applied for the determination of PAHs in three commercial infusion solutions and in nine different medications stored in syringes prior to administration to patients. Twelve of 16 PAHs were found in these samples. Total PAH concentrations varied from 0.13 to 13.50 mu g/mL. Pyrene was the most prevalent contaminant, being present in 11 of 12 samples in concentrations ranging from 0.17 to 4.80 mu g/mL. This method presented good sensitivity for the measurement of PAH in the target samples, allowing for the determination of the 16 priority PAHs in one run and in 30 min.
机译:提出了HPLC耦合到UV二极管阵列检测(爸爸),用于测定肠胃外给药的药物产品中的多环芳烃(PAH)。由于橡胶是这些产品的PAHS可能的来源,所以选择储存在具有橡胶部件的容器中的样品进行分析。方法优化的基础是EPA方法8310,其使用紫外线和荧光检测通过HPLC确定接地水和废水中的16个优先级PAH。使用爸爸,选择两个通道进行检测,其中一个在254nm下工作,用于检测九个PAHs,另一个在225nm处检测七个PAHs。该方法允许使用用腰部的外部校准检测PAHs,LOQ分别从0.001至0.060μg/ ml和0.003〜0.167μg/ ml检测。在与RSD表示为RSD的日内精度范围内,PAH浓度为0.05至0.50μmg/ ml的1.24〜7.76%,而盘子内精度在相同的浓度范围内的3.10至9.40%变化。通过掺入样品的75-120%的回收率证实了方法准确性。应用该方法用于在给予患者之前在三种商业输注溶液中测定三种商业输注溶液中的PAHS,并含有九种不同的药物。在这些样品中发现了12种16个PAH。总PAH浓度从0.13变化0.13至13.50μg/ ml。芘是最普遍的污染物,存在于12个样品中的11个,其浓度范围为0.17至4.80μmg/ ml。该方法呈现了对靶样品中PAH测量的良好敏感性,允许在一次运行和30分钟内确定16个优先级PAHs。

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