Work

Development of a Captiva EMR-lipid clean-up and LC-MS/MS methodology for detecting H2 receptor antagonists in functional foods and food-medicine homology materials

Year: 2025
Type: article
Abstract: • New method combines CEL-SPE with LC-MS/MS to detect H2RAs in FFs and FMHs. • Captiva EMR-Lipid SPE removes interferences, enhancing sensitivity and accuracy. • Optimized conditions yield high precision, recovery rates, and low detection limits. • It offers effective means to ensure product safety and consumer health. The inappropriate use of H2 receptor antagonists (H2RAs) in functional foods (FFs) and food-medicine homology materials (FMHs) designed to enhance gastrointestinal function (IGF) presents health risks due to potential adverse effects. In this study, an analytical method that integrates Captiva EMR-Lipid (CEL) solid-phase extraction (SPE) with liquid chromatography tandem mass spectrometry (LC-MS/MS) has been developed for the detection of H2RAs (nizatidine, famotidine, cimetidine, ranitidine, and lafutidine) in these products. Through the optimization of CEL-SPE parameters, such as using 200 mg of sorbent and eluting with ACN/water (80/20, v/v), the recovery rates of H2RAs in IGF-FF and IGF-FMH ranged from 87.4% to 94.6% and 90.2% to 97.1%, respectively. The assessment of matrix effects revealed that the five H2RAs exhibit matrix suppression, necessitating the construction of matrix-matched standard curves with correlation coefficients (r 2 ) exceeding 0.9991. The detection limits ranged from 0.4 to 0.8 μg·kg −1 and the quantification limits ranged from 1.3 to 2.7 μg·kg −1 , with recovery rates spanning from 85.4% to 97.1% and relative standard deviations ≤ 15%. The successful development of this technique not only helps safeguard consumer health but also provides scientific basis and technical support for market supervision, thereby preventing and addressing food safety risks.
Language: English
Field: Chemistry
Open Access status: gold
Estimated APC paid: $2,050
OpenAlex ID: W4407397993
FWCI: 2.21
Cites: 23
Cited by: 6
Related to: 10