Non-Steroidal Anti-Inflammatory Drugs Current Challenges and Future Perceptions

K. Malleswari⃰, D. R. Reddy, K. C. Sri, D. B. Vali, G. Suresh
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引用次数: 0

Abstract

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 1 (SPE–UHPLC–MS/MS). Extraction conditions were optimized taking into account parameters like sorbent material, sample volume and sample 1,2 PH. Method detection limits (MDLs) ranging from 0.02 to 8.18 ng/L were obtained 2,3. 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 hydroxy ibuprofen being the most frequently detected at concentrations that can reach some hundreds of ng/L 4.
非甾体抗炎药当前的挑战和未来的看法
建立了离线固相萃取-超高效液相色谱-串联质谱联用(SPE-UHPLC-MS /MS)同时测定非甾体抗炎药(NSAIDs)和镇痛药治疗组7种药物和2种代谢物的分析方法。考虑吸附剂材料、样品体积和样品1,2 ph等参数对提取条件进行优化。方法检出限(MDLs)范围为0.02 ~ 8.18 ng/L 2、3。该方法成功地应用于葡萄牙北部海岸大西洋海水样品中选定药物的测定。所有的药物都在海水样本中被检测到,像布洛芬、对乙酰氨基酚、酮洛芬和代谢物羟基布洛芬这样的药物是最常被检测到的,其浓度可以达到几百ng/L 4。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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