首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Multi-residue analysis of chiral and achiral trace organic contaminants in soil by accelerated solvent extraction and enantioselective liquid chromatography tandem-mass spectrometry
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Multi-residue analysis of chiral and achiral trace organic contaminants in soil by accelerated solvent extraction and enantioselective liquid chromatography tandem-mass spectrometry

机译:加速溶剂萃取和对映选择性液相色谱串联光谱法对土壤手性和成立痕量有机污染物的多残基分析

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Reported here is the first analytical methodology for the enantiomeric determination of chiral trace organic contaminants (TOrCs) in soil. Direct enantioselective separations were achieved on a Chirobiotic V2 (R) column operated in polar ionic mode. Initial screening of vancomycin stationary phases found Chirobiotic V2 (R) better suited for multi-residue separation of chiral TOrCs than Chirobiotic V (R) due to differences in the ligand linkage chemistry. Simultaneous enantioseparati on of beta-blockers, beta-agonists, anti-depressants, anti-histamines and stimulants was achieved for the first time. This included the first separation of chlorpheniramine enantiomers with a method suitable for environmental analysis (i.e., coupled to MS). Investigation of mobile phase composition found the concentration of liophilic ions had the greatest influence on enantioseparations and of most importance during method development. The optimized method achieved simultaneous separation of salbutamol, propranolol, atenolol, amphetamine, chlorpheniramine and fluoxetine enantiomers with satisfactory resolution (1.0). For completeness, such methods also need to support analysis of achiral TOrCs. Therefore three achiral TOrCs (carbamazepine, carbamazepine 10,11 epoxide and triclocarban) were included to demonstrate the methods suitability. Method recoveries for all analytes ranged from 76 to 122% with method quantitation limits (MQLs) 1 ng g(-1). Application of the method to soil microcosm studies revealed stereoselective degradation of chiral TOrCs for the first time. For example, S(+)-amphetamine degraded at a faster rate than its corresponding enantiomer leading to an enrichment of R(-)-amphetamine. Therefore to better understand the risk posed from TOrCs on the terrestrial environment, chiral species need profiled at the enantiomeric level. This can now be addressed using the proposed methodology whilst simultaneously profiling achiral TOrCs. (C) 2018 Elsevier B.V. All rights
机译:这里报道的是第一种分析方法用于对土壤中手性痕量有机污染物(TORC)的对映体测定的分析方法。在极性离子模式下操作的膀胱族V2(R)柱上实现了直接对映选择性分离。初始筛选万古霉素固定相,由于配体键化化学的差异,发现更适合于多残基分离的阴茎v2(r),而不是脊髓慢性v(r)。首次实现了β-嵌体,β-激动剂,抗抑郁药,抗组胺和刺激物的同时对映对映对映对。这包括一种适用于环境分析的方法的第一次分离氯苯那甲酰映异构体(即,耦合到MS)。流动相组成的调查发现,在方法开发过程中对酶部进行的影响和最重要的影响最大。优化方法通过令人满意的分辨率(& 1.0),实现了同时分离沙丁酰胺,普萘洛尔,阿替洛尔,苯甲酸,丙醇,阿米兰醇,苯甲酸丁胺,氟甲胺对映异构体。为了完整性,这些方法还需要支持对成立TORC的分析。因此,包括三个成立的TORC(尿嘧啶,尸毒甲酰胺10,11环氧化物和三氧化物)以证明方法适用性。对于所有分析物的方法回收率范围为76至122%,方法定量限制(MQLS)<1 ng(-1)。该方法在土壤微科本研究中的应用揭示了第一次手性扭矩的立体选择性降解。例如,S(+) - amphetamine以比其相应的对映体更快的速率降解,导致R( - ) - amphetamine的富集。因此,为了更好地了解从陆地环境上从TORCS构成的风险,手性物种需要在对映体水平上进行异形。现在可以使用所提出的方法来解决这一方法,而同时分析成立的TORC。 (c)2018 Elsevier B.V.所有权利

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