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Molecularly imprinted solid‐phase extraction coupled with LC–APCI–MS–MS for the selective determination of serum cholesterol
Author(s) -
Matos Cordeiro Borges Marcella,
Leijoto de Oliveira Hanna,
Bastos Borges Keyller
Publication year - 2017
Publication title -
electrophoresis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.666
H-Index - 158
eISSN - 1522-2683
pISSN - 0173-0835
DOI - 10.1002/elps.201600489
Subject(s) - atmospheric pressure chemical ionization , chromatography , molecularly imprinted polymer , chemistry , solid phase extraction , analytical chemistry (journal) , mass spectrometry , extraction (chemistry) , sample preparation , detection limit , ionization , selectivity , chemical ionization , ion , biochemistry , organic chemistry , catalysis
The assessment of selective molecularly imprinted solid‐phase extraction (MISPE) for clean‐up and extraction of cholesterol (CHO) from bovine and human serum samples was evaluated. Two molecular imprinted polymers (MIP) based on organic and inorganic/organic (hybrid) materials were obtained and compared regarding recovery and selectivity toward CHO. Optimum chromatographic separation between the CHO and its isobaric compound lathosterol (LATHO) has been achieved within 15 min using an Agilent Poroshell 120 EC‐C18 column (120 mm × 3.0 mm, 2.7 μM) and mobile phase consisting of acetonitrile:methanol (8:2, v/v) at a flow rate of 0.6 mL min −1 . Mass spectrometry detection was operated in atmospheric pressure chemical ionization (APCI) (+) mode and the SIM transitions [M – H 2 O + H] + for CHO and LATHO were 364.1 → 161.2 → 95.2 and 364.1 → 95.1 → 81.1 m / z , respectively. The sample preparation could be accomplished within 1 h, and the matrix effect on the MS signal after sample pretreatment did not interfere in the analyses. The method provided a good linear range (0.013–312 μM.) with coefficients of determination of R 2 > 0.99, substantial sensitivity (limits of detection of 6.5 nM), good recovery (∼90%), high reproducibility (intraday and interday relative standard deviations less than 15%) and satisfactory accuracy (relative error ranged from –13.46% to 11.54%). The organic MIP showed superior performance compared with the hybrid. Finally, the MISPE procedure followed by LC–APCI–MS–MS analysis showed their suitable applicability to examine CHO and LATHO in serum samples.