Guo Ping, Zhang Jingjing, Chen Xiaohui, Zhao Longshan
School of Pharmacy, Shenyang Pharmaceutical University, Shenyang, China.
Biomed Chromatogr. 2018 Jun;32(6):e4193. doi: 10.1002/bmc.4193. Epub 2018 Feb 22.
A molecularly imprinted polymer was synthesized and applied as a sorbent in the solid-phase extraction device. The imprinted polymer was characterized by fourier-transform infrared spectroscopy and scanning electron microscope. The results revealed that imprinted polymer possess sensitive selectivity and reliable adsorption properties for five NSAIDs. The imprinted polymer was successfully applied to the pre-concentration for five NSAIDs in different water samples prior to UPLC-MS/MS. In the early studies, several factors were investigated, including pH adjustment, the kind of elution solvent and the volume of elution solvent. Finally, we found that the pH 5 and an aliquot of 2 mL methanol were suitable for the water samples. The limits of detection and limits of quantitation of five nonsteroidal anti-inflammatory drugs varied from 0.007 to 0.480 μg L and 0.03 to 1.58 μg L , respectively. The spiking recoveries of the target analytes were 50.33-127.64% at the levels of 0.2 μg L , 2 μg L and 5 μg L . The precision and accuracy of this method showed a great increase compared with traditional solid-phase extraction. The developed method was successfully applied to extraction and analysis of NSAIDs in different water samples with satisfactory results which could help us better understand their environmental fate and risk to ecological health.
合成了一种分子印迹聚合物,并将其用作固相萃取装置中的吸附剂。通过傅里叶变换红外光谱和扫描电子显微镜对印迹聚合物进行了表征。结果表明,印迹聚合物对五种非甾体抗炎药具有灵敏的选择性和可靠的吸附性能。该印迹聚合物成功应用于不同水样中五种非甾体抗炎药的超高效液相色谱-串联质谱分析前的预浓缩。在早期研究中,研究了几个因素,包括pH调节、洗脱溶剂的种类和洗脱溶剂的体积。最后,我们发现pH 5和2 mL甲醇的等分试样适用于水样。五种非甾体抗炎药的检测限和定量限分别为0.007至0.480 μg/L和0.03至1.58 μg/L。在0.2 μg/L、2 μg/L和5 μg/L水平下,目标分析物的加标回收率为50.33-127.64%。与传统固相萃取相比,该方法的精密度和准确度有了很大提高。所建立的方法成功应用于不同水样中NSAIDs的萃取和分析,结果令人满意,有助于我们更好地了解它们的环境归宿和对生态健康的风险。