Barichello Marcia M, Bohrer Denise, Viana Carine, Carvalho Leandro M, Nascimento Paulo C
Federal University of Santa Maria, Postgraduate Program in Pharmaceutical Sciences, Avenida Roraima 1000, Santa Maria 97105-900, Brazil.
Federal University of Santa Maria, Department of Chemistry, Avenida Roraima 1000, Santa Maria, 97105-900, Brazil.
J AOAC Int. 2017 Jul 1;100(4):1070-1076. doi: 10.5740/jaoacint.16-0342.
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 µg/mL and from 0.003 to 0.167 µg/mL, respectively. Within-day precision, expressed as RSD, varied from 1.24 to 7.76% for PAH concentrations from 0.05 to 0.50 µg/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 µg/mL. Pyrene was the most prevalent contaminant, being present in 11 of 12 samples in concentrations ranging from 0.17 to 4.80 µg/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.
本文提出采用高效液相色谱法(HPLC)结合紫外二极管阵列检测(DAD)来测定非肠道给药药品中的多环芳烃(PAHs)。由于橡胶可能是这些产品中多环芳烃的一个来源,因此选择储存在带有橡胶部件容器中的样品进行分析。方法优化的依据是美国环保署(EPA)方法8310,该方法通过HPLC同时使用紫外和荧光检测来测定地下水和废水中的16种优先多环芳烃。使用DAD时,选择两个通道进行检测,一个在254nm处运行以检测9种多环芳烃,另一个在225nm处运行以检测7种多环芳烃。该方法采用外标法检测多环芳烃,检测限(LOD)和定量限(LOQ)分别为0.001至0.060μg/mL和0.003至0.167μg/mL。日内精密度以相对标准偏差(RSD)表示,对于浓度为0.05至0.50μg/mL的多环芳烃,其范围为1.24至7.76%,对于相同浓度范围,日间精密度范围为3.10至9.40%。通过加标样品75-120%的回收率确认了方法的准确性。该方法用于测定三种市售输液溶液以及在给患者给药前储存在注射器中的九种不同药物中的多环芳烃。在这些样品中发现了16种多环芳烃中的12种。多环芳烃的总浓度范围为0.13至13.50μg/mL。芘是最普遍的污染物,在12个样品中的11个中存在,浓度范围为0.17至4.80μg/mL。该方法对目标样品中多环芳烃的测量具有良好的灵敏度,能够在一次运行和30分钟内测定16种优先多环芳烃。