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A generic approach for expanding homolog-targeted residue screening of sulfonamides using a fast matrix separation and class-specific fragmentation-dependent acquisition with a hybrid quadrupole-linear ion trap mass spectrometer
被引:39
作者:
Huang, Chunlin
[2
]
Guo, Bin
[1
]
Wang, Xiaoying
[1
]
Li, Jie
[2
]
Zhu, Weitao
[1
]
Chen, Bo
[1
]
Ouyang, Shan
[3
]
Yao, Shouzhuo
[1
]
机构:
[1] Hunan Normal Univ, Minist Educ China, Key Lab Chem Biol & Tradit Chinese Med Res, Changsha 410081, Hunan, Peoples R China
[2] Univ S China, Sch Pharm & Life Sci, Dept Biochem & Mol Biol, Hengyang 421001, Peoples R China
[3] Shenzhen Entry Exit Inspect & Quarantine Bur Peop, Food Inspect & Quarantine Ctr, Shenzhen 518067, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Sulfonamides;
Multi-residue;
Dispersive solid-phase extraction;
Animal tissues;
Triple-quadrupole linear ion trap mass;
spectrometer;
Semi-targeted screening;
PERFORMANCE LIQUID-CHROMATOGRAPHY;
VETERINARY DRUG RESIDUES;
SOLID-PHASE EXTRACTION;
DEGRADATION-PRODUCTS;
ENVIRONMENTAL WATERS;
HUMAN URINE;
METABOLITES;
ANTIBIOTICS;
FOOD;
IDENTIFICATION;
D O I:
10.1016/j.aca.2012.05.041
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
A generic and efficient homolog-targeted approach was used to expand screening and detection of target class of sulfonamides and structural analogs, based on a fast single-tube extraction/partitioning-multifunction adsorption cleanup (SEP/MAC) for class-specific fragmentation-dependent acquisition with a liquid chromatography-hybrid triple-quadrupole linear ion trap mass spectrometer (LC-QqLIT). By combining the two-stage process conducted in a single tube as one-pot protocol, the straightforward SEP/MAC procedure was optimized to offer clean extracts with reasonable recovery (71-109% with RSDs < 20%) and decreased matrix interferences (-9 to 19%) of multiresidual sulfonamide extraction from different tissue samples. The novel use of neutral loss scan of 66 Da (NLS) or precursor ion scanning of m/z 108 (PreS) in positive ion mode was found to achieve more comprehensive coverage of protonated molecular ions of a wide array of sulfonamides including N-4-acetyl and hydroxylamine metabolites plus their possible dimers. Moreover, the PreS-triggered automatically enhanced product ion spectral acquisition enabled simultaneous screening, profiling and confirmation of an unlimited number of analytes belonging to the sulfonamide class within a single analysis. The validation and application results of the generic SEP/MAC-based LC-QqLIT strategy consistently demonstrated favorable performances with acceptable accuracy (67-116%), precision (RSDs < 25%), and sensitivity (LOQs <= 7.5 ng g(-1)) to meet the acceptance criteria for all the sulfonamide-tissue combinations. Thus, the integration of the matrix-independent SEP/MAC procedure and the multiparameter matching algorithm with the unit-resolution LC-QqLIT instrument can serve as a valuable semi-targeted discovery strategy for rapid screening and reliable quantitative/confirmatory analysis of real samples. (C) 2012 Elsevier B.V. All rights reserved.
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页码:83 / 98
页数:16
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