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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Periodic mesoporous organosilica materials as sorbents for solid-phase extraction of drugs prior to simultaneous enantiomeric separation by capillary electrophoresis
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Periodic mesoporous organosilica materials as sorbents for solid-phase extraction of drugs prior to simultaneous enantiomeric separation by capillary electrophoresis

机译:通过毛细管电泳同时对映体分离之前,定期介孔有机溶胶作为用于固相萃取药物的吸附剂

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Two novel periodic mesoporous organosilica materials were synthesized with a neutral phenylenebridged ligand, 1,4-bis(trimethoxysilylethyl)benzene, one of them using tetraethyl orthosilicate as additional silica source (PMO-TMSEB-1 and PMO-TMSEB-2). A third material was also synthesized with 1,4-bis(triethoxysilyl)benzene ligand (PMO-TESB-1) which use has scarcely been reported. The three materials were evaluated as solid-phase extraction (SPE) sorbents for the off-line extraction of a mixture of seven drugs of different nature (duloxetine, terbutaline, econazole, propranolol, verapamil, metoprolol, and betaxolol) from water samples. Subsequent simultaneous enantiomeric analysis by CE, using sulfated-beta-cyclodextrin (2% w/v) dissolved in a 25 mM phosphate buffer (pH 3.0) and a voltage of -20 kV (negative polarity) was carried out. Enantiomeric resolutions ranging from 2.4 to 8.5 were obtained in an analysis time of 16 min. After optimization of SPE parameters, it was shown that using just 100 mg of PMO-TESB-1 as sorbent, a preconcentration factor of 400 with 200 mL solution was achieved, allowing recoveries between 80.5 and 103.1% (except for terbutaline), with good repeatability (% RSD = 2-8 %, n = 5). Analytical characteristics of the method were evaluated in terms of precision, linearity and accuracy with method quantitation limits between 5.6 and 21.9 mu g/L. The developed method was applied to the analysis of spiked wastewater samples collected in different treatment plants, with recoveries between 73.9 and 102.9% except for econazole with recovery values ranging between 58.5 and 72.4%. (C) 2018 Elsevier B.V. All rights reserved.
机译:用中性亚苯基杂交配体,1,4-双(三甲氧基甲硅烷基甲基)苯,使用四乙基硅胶作为另外的二氧化硅源(PMO-TMSEB-1和PMO-TMSEB-2),用中性亚苯基杂交配体,1,4-双(三甲氧基甲硅烷甲甲乙基)苯。还用1,4-双(三乙氧基甲硅烷基)苯配体(PMO-TESB-1)合成第三种材料,该苯配体几乎没有报道。将三种材料评价为固相萃取(SPE)吸附剂,用于偏离水样(Duloxetine,Terbutaline,Econazole,丙唑醇,尿嘧啶,甲唑,甲基唑和甲肾上腺素)的偏离线提取。通过Ce的后续对映体分析,使用溶解在25mM磷酸盐缓冲液(pH3.0)中的硫酸盐 - β-环糊精(2%w / v)和-20kV(负极性)的电压进行。在16分钟的分析时间中获得的对映体分辨率为2.4至8.5。在优化SPE参数后,显示使用仅100mg PMO-TESB-1作为吸附剂,实现了400个具有200ml溶液的预浓度率,允许回收80.5和103.1%(特许碱除外),良好重复性(%RSD = 2-8%,n = 5)。根据精度,线性度和精度评估方法的分析特性,方法定量限制在5.6和21.9μg/ L之间。除了生态氧唑之外,将研制方法应用于不同治疗植物中收集的尖刺废水样品的分析,恢复在73.9和102.9%之间,恢复值范围为58.5和72.4%。 (c)2018年elestvier b.v.保留所有权利。

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