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Quantification of selected pharmaceutical compounds in water using liquid chromatography-electrospray ionisation mass spectrometry (LC-ESI-MS)

机译:使用液相色谱 - 电喷雾电离质谱法(LC-ESI-MS)定量水中所选药物化合物

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摘要

The detection and quantitation of pharmaceutical compounds (PCs) in different environmental matrices is still a challenge, due to their extremely low (ng-μg) concentrations and the lack of rapid and sensitive analytical techniques. A number of techniques, such as enzyme-linked immunosorbent assay (ELISA), chromatography, electrophoresis, and electrochemical methods have been explored. These methods are limited by their poor sensitivity. In this study, a hyphenated liquid chromatography-mass spectrometric (LC-MS) method was developed, validated, and tested for the detection and quantification of seven active pharmaceutical compounds, with solid-phase extraction for analytes recovery and separation of interference from the aqueous matrix. The sensitivity achieved for the method allowed for LODs (μg/L) of 0.0439, 0.0684, 0.1219, 0.0710, 0.1129, 0.0447, 0.0837 and LOQs (μg/L) of 0.1462, 0.2281, 0.4065, 0.2367, 0.3763, 0.1492, 0.2792, for lamivudine, acetaminophen, vancomycin, ciprofloxacin, sulfamethoxazole, diclofenac, and ivermectin, respectively, within a linear range of 0.01–0.1 μg/mL. Other ICH validation parameters are also discussed. The different PCs were positive in 61 % of the tested surface waters, with diclofenac present only in two of the sampling points. The concentrations at which they occurred were variable and ranged between ND and 398.98 μg/L.
机译:由于其极低(Ng-μg)浓度和缺乏快速敏感的分析技术,不同环境基质中药物化合物(PCS)的检测和定量仍是一个挑战。已经探讨了许多技术,例如酶联免疫吸附测定(ELISA),色谱,电泳和电化学方法。这些方法受其敏感性差的限制。在本研究中,开发,验证,验证,验证,验证,验证,验证和定量七种活性药物化合物的检测和定量,用于分析物的固相萃取和与水性干扰分离矩阵。允许允许0.0439,0.0684,0.1219,0.0710,0.1129,0.047,0.0837和loqs(μg/l)的腰液(μg/l)的敏感性为0.1462,0.2281,0.4065,0.2367,0.3763,0.1492,0.2792,对于拉米夫定,乙酰氨基酚,万古霉素,环丙沙星,磺胺甲嘧辛,双氯芬酸和伊维菌素分别在0.01-0.1μg/ ml的线性范围内。还讨论了其他ICH验证参数。不同的PC在61%的测试表面水中是阳性的,用双氯芬酸仅存在于两种采样点。它们发生的浓度是可变的并且在Nd和398.98μg/ l之间进行。

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