Paíga Paula, Lolić Aleksandar, Hellebuyck Floris, Santos Lúcia H M L M, Correia Manuela, Delerue-Matos Cristina
REQUIMTE, Instituto Superior de Engenharia do Porto, Instituto Politécnico do Porto, Rua Dr. António Bernardino de Almeida, 431, 4200-072 Porto, Portugal.
REQUIMTE, Instituto Superior de Engenharia do Porto, Instituto Politécnico do Porto, Rua Dr. António Bernardino de Almeida, 431, 4200-072 Porto, Portugal; Faculty of Chemistry, University of Belgrade, Studentski trg 12-16, 11158 Belgrade, Serbia.
J Pharm Biomed Anal. 2015 Mar 15;106:61-70. doi: 10.1016/j.jpba.2014.06.017. Epub 2014 Jun 23.
An analytical methodology for the simultaneous determination of seven pharmaceuticals and two metabolites belonging to the non-steroidal anti-inflammatory drugs (NSAIDs) and analgesics therapeutic groups was developed based on off-line solid-phase extraction and ultra-high performance liquid chromatography coupled to tandem mass spectrometry (SPE-UHPLC-MS/MS). Extraction conditions were optimized taking into account parameters like sorbent material, sample volume and sample pH. Method detection limits (MDLs) ranging from 0.02 to 8.18 ng/L were obtained. This methodology was successfully applied to the determination of the selected pharmaceuticals in seawater samples of Atlantic Ocean in the Northern Portuguese coast. All the pharmaceuticals have been detected in the seawater samples, with pharmaceuticals like ibuprofen, acetaminophen, ketoprofen and the metabolite hydroxyibuprofen being the most frequently detected at concentrations that can reach some hundreds of ng/L.
基于离线固相萃取和超高效液相色谱-串联质谱联用技术(SPE-UHPLC-MS/MS),开发了一种同时测定七种属于非甾体抗炎药(NSAIDs)和镇痛药治疗组的药物及两种代谢物的分析方法。考虑到吸附剂材料、样品体积和样品pH值等参数,对萃取条件进行了优化。获得了0.02至8.18 ng/L的方法检测限(MDLs)。该方法成功应用于葡萄牙北部海岸大西洋海水样品中所选药物的测定。在海水样品中均检测到了所有药物,其中布洛芬、对乙酰氨基酚、酮洛芬和代谢物羟基布洛芬等药物最常被检测到,其浓度可达数百ng/L。