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Determination of statin drugs in hospital effluent with dispersive liquid-liquid microextraction and quantification by liquid chromatography

机译:分散液-液微萃取-液相色谱法测定医院废水中他汀类药物

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Statins are classified as being amongst the most prescribed agents for treating hypercholesterolaemia and preventing vascular diseases. In this study, a rapid and effective liquid chromatography method, assisted by diode array detection, was designed and validated for the simultaneous quantification of atorvastatin (ATO) and simvastatin (SIM) in hospital effluent samples. The solid phase extraction (SPE) of the analytes was optimized regarding sorbent material and pH, and the dispersive liquid-liquid microextraction (DLLME), in terms of pH, ionic strength, type and volume of extractor/dispersor solvents. The performance of both extraction procedures was evaluated in terms of linearity, quantification limits, accuracy (recovery %), precision and matrix effects for each analyte. The methods proved to be linear in the concentration range considered; the quantification limits were 0.45 mg L-1 for ATO and 0.75 mg L-1 for SIM; the matrix effect was almost absent in both methods and the average recoveries remained between 81.5-90.0%; and the RSD values were <20%. The validated methods were applied to the quantification of the statins in real samples of hospital effluent; the concentrations ranged from 18.8 mg L-1 to 35.3 mg L-1 for ATO, and from 30.3 mg L-1 to 38.5 mg L-1 for SIM. Since the calculated risk quotient was <= 192, the occurrence of ATO and SIM in hospital effluent poses a potential serious risk to human health and the aquatic ecosystem.
机译:他汀类药物被归类为治疗高胆固醇血症和预防血管疾病的最处方药物。在这项研究中,设计并验证了一种快速有效的液相色谱方法,并辅以二极管阵列检测技术,可同时定量分析医院废水样品中的阿托伐他汀(ATO)和辛伐他汀(SIM)。就吸附剂材料和pH以及分散液-液微萃取(DLLME)的pH,离子强度,萃取器/分散器溶剂的类型和体积进行了优化,对分析物的固相萃取(SPE)进行了优化。根据线性,定量限,准确性(回收率%),精密度和每种分析物的基质效应,对两种萃取程序的性能进行了评估。该方法在所考虑的浓度范围内被证明是线性的。 ATO的定量限为0.45 mg L-1,SIM的定量限为0.75 mg L-1。两种方法几乎都没有基质效应,平均回收率保持在81.5-90.0%之间。 RSD值<20%。经验证的方法用于医院流出液实际样品中他汀类药物的定量; ATO的浓度范围为18.8 mg L-1至35.3 mg L-1,SIM的浓度范围为30.3 mg L-1至38.5 mg L-1。由于计算的风险商<= 192,因此在医院废水中发生ATO和SIM会对人体健康和水生生态系统构成潜在的严重风险。

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