Molecularly imprinted solid‐phase extraction coupled with LC–APCI–MS–MS for the selective determination of serum cholesterol

Abstract

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 . Mass spectrometry detection was operated in atmospheric pressure chemical ionization (APCI) (+) mode and the SIM transitions [M - H 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 > 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.

Rational design of a molecularly imprinted polymer for dinotefuran: theoretical and experimental studies aimed at the development of an efficient adsorbent for microextraction by packed sorbent

“…Low-porosity polymers with a small surface area have a low molecular recognition capacity, basically due to the slow diffusion of the analytes towards the selective sites located in the micropores. [39][40][41][42][43][44] Therefore, the morphological structures of NIP and MIP were investigated by SEM. Fig.…”

“…S6(C and D) † shows the curves obtained by TGA, performed in a temperature range of 25 to 600 °C for the NIP and MIP. Our research group has been working on the synthesis of MIP using MAA as FM, [39][40][41][42][43][44] in which it is possible to determine the presence of three main thermal events. The first one (between approximately 25 and 80 °C) presents a small loss of mass due to the evaporation of residual water.…”