Coupling Solid-Phase Microextraction with Ambient Mass Spectrometry Using Surface Coated Wooden-Tip Probe for Rapid Analysis of Ultra Trace Perfluorinated Compounds in Complex Samples

被引:104
作者
Deng, Jiewei [1 ]
Yang, Yunyun [2 ]
Fang, Ling [3 ]
Lin, Li [1 ]
Zhou, Haiyun [3 ]
Luan, Tiangang [1 ]
机构
[1] Sun Yat Sen Univ, Sch Life Sci, MOE, Key Lab Aquat Prod Safety, Guangzhou 510275, Guangdong, Peoples R China
[2] China Natl Analyt Ctr Guangzhou, Guangdong Prov Publ Lab Anal & Testing Technol, Guangzhou 510070, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Instrumental Anal & Res Ctr, Guangzhou 510275, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
DESORPTION ELECTROSPRAY-IONIZATION; TEMPERATURE PLASMA PROBE; ATMOSPHERIC-PRESSURE; REAL-TIME; IN-VIVO; PAPER SPRAY; ION-SOURCE; WATER; SILANIZATION; EXTRACTION;
D O I
10.1021/ac5034177
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Coupling solid-phase microextraction (SPME) with ambient mass spectrometry using surface coated woodentip probe was achieved for the first time and applied in the analysis of ultra trace perfluorinated compounds (PFCs) in complex environmental and biological samples. We modified n -octadecyldim ethyl [3- (trim ethoxysily1) propyl] amrn onium chloride on the surface of sharp wooden tip via silanization to form a novel SPME probe, which was then used for highly selective enrichment of PFCs from complex matrices and applied as a solid substrate to induce electrospray ionization for mass spectrometric analysis. The porous structural surface together with the dual extraction mechanisms (reversed phase adsorption and ion exchange adsorption) demonstrated that the SPME probe has an outstanding enrichment capacity, enhancing sensitivity by approximately 4000-8000 folds for the detection in aqueous samples, and 100-500-fold in whole blood and milk samples. The method showed good linearity, with correlation coefficient values (r(2)) of no less than 0.9931 for eight target PFCs. The limits of detection and qualification of the eight PFCs were 0.06-0.59 and 0.21-1.98 ng/L, respectively. Quantification of real samples was achieved by isotope internal standard calibration curve method or isotope dilution method, and ultratrace levels of PFCs present in lake water, river water, whole blood, and milk samples had been successfully detected and qualified.
引用
收藏
页码:11159 / 11166
页数:8
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