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Microwave-assisted esterification and electro-enhanced solid-phase microextraction of omega-3 polyunsaturated fatty acids in eggs. | LitMetric

Microwave-assisted esterification and electro-enhanced solid-phase microextraction of omega-3 polyunsaturated fatty acids in eggs.

Food Chem

State Key Laboratory of Food Science and Resources, School of Food Science and Technology, Collaborative Innovation Center of Food Safety and Quality Control in Jiangsu Province, Jiangnan University, Wuxi 214122, China; International Joint Laboratory on Food Safety, Jiangnan University, Wuxi 214122, China. Electronic address:

Published: August 2024

AI Article Synopsis

  • Researchers developed a new technique for efficiently extracting omega-3 polyunsaturated fatty acids (ω-3 PUFAs) from eggs using microwave-assisted esterification (MAE) and electrically enhanced solid-phase microextraction (EE-SPME).
  • The microwave method significantly increased esterification efficiency by up to 10.65 times, while EE-SPME reduced extraction time from 50 minutes to just 15 minutes.
  • The optimized method achieved low detection limits, high recovery rates, and a wide linear range, enabling effective analysis of ω-3 PUFAs in real egg samples.

Article Abstract

Omega-3 polyunsaturated fatty acids (ω-3 PUFAs), a type of fatty acid that has many health benefits, are of increasing concern. Herein, we developed a method for the rapid esterification and enrichment of ω-3 PUFAs in eggs, which includes microwave-assisted esterification (MAE) and electrically enhanced solid-phase microextraction (EE-SPME). Combined with gas chromatographic, efficient detection of ω-3 PUFAs was achieved in eggs. Under microwave radiation, the esterification efficiency exhibited a significant increase ranging from 5.06 to 10.65 times. The EE-SPME method reduced extraction time from 50 to 15 min. In addition, improvements in extractive fiber coating materials were explored, which ensured efficient extraction of ω-3 PUFAs. Under the optimal conditions, the method displayed a low detection limit (1.01-1.54 μg L), good recoveries (85.82%-106.01%), and wide linear range (7.5-1000 μg L), which was successfully applied to determine ω-3 PUFAs in real egg samples.

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Source
http://dx.doi.org/10.1016/j.foodchem.2024.139060DOI Listing

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