Molecularly imprinted polymers as analyte sequesters and selective surfaces for easy ambient sonic-spray ionization

被引:55
作者
Figueiredo, Eduardo Costa [1 ,2 ]
Sanvido, Gustavo Braga [2 ]
Zezzi Arruda, Marco Aurelio [3 ,4 ]
Eberlin, Marcos Nogueira [2 ]
机构
[1] Univ Fed Alfenas, Dept Clin & Toxicol Anal, BR-37130000 Alfenas, MG, Brazil
[2] Univ Estadual Campinas, ThoMSon Mass Spectrometry Lab, Inst Chem, BR-13083970 Campinas, SP, Brazil
[3] Univ Estadual Campinas, Inst Chem, Grp Spectrometry Sample Preparat & Mechanizat GEP, BR-13083970 Campinas, SP, Brazil
[4] Univ Estadual Campinas, Inst Chem, Natl Inst Sci & Technol Bioanalyt, BR-13083970 Campinas, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
SOLID-PHASE EXTRACTION; MASS-SPECTROMETRY; RECOGNITION;
D O I
10.1039/b923289c
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The use of a molecularly imprinted polymer (MIP) as a selective surface for ambient mass spectrometry is demonstrated. The MIP is used to sequester target analytes from urine and easy ambient sonic-spray ionization mass spectrometry (EASI-MS) is shown to be able to efficiently desorb the analytes from the MIP surface and then transfer them in protonated forms to the gas phase for MS analysis. A set of five phenothiazines (chlorpromazine, perphenazine, triflupromazine, thioridazine and prochlorperazine) were chosen from a proof-of-principle class of drug samples. A chlorpromazine-imprinted methacrylic polymer was synthesized and used to prepare a MIP probe. The MIP-EASI-MS technique using acidified methanol as solvent has been shown to allow quantification of all five drugs in urine with LOQ of ca. 1 mu mol L(-1).
引用
收藏
页码:726 / 730
页数:5
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