AI Article Synopsis

  • Eriocitrin, a key compound in lemons, has notable health benefits including antioxidant, anticancer, and anti-inflammatory properties, and is commonly used in food and beverages.
  • A new LC/MS/MS method was developed to efficiently analyze eriocitrin levels in rat plasma, ensuring precision and accuracy in the measurements.
  • The pharmacokinetic study revealed the maximum concentration of eriocitrin in plasma, how long it takes to peak, and its half-life, providing foundational data for future research.

Article Abstract

Eriocitrin is one of the major active constituents of lemon fruit, and it possesses strong antioxidant, lipid-lowering, anticancer and anti-inflammatory activities and has long been used in food, beverages and wine. In this study, for the first time, a rapid, selective, and sensitive liquid chromatography-tandem mass spectrometry method (LC/MS/MS) with protein precipitation was developed and validated for the analysis of eriocitrin in rat plasma. Chromatographic separation was achieved using a mobile phase, comprising 0.1% formic acid aqueous solution and acetonitrile eluted at a flow rate of 0.8 mL min. In multiple reaction monitoring (MRM) modes, eriocitrin and internal standard (IS) were quantified using precursor-to-product ion transitions of / 595.4 → 287.1 and / 252.0 → 155.9, respectively. The intra- and inter-day precision (RSD) were below 6.79% in plasma, while accuracy (RE) was within ±7.67%. The matrix effect, recovery and stability were also demonstrated to be within acceptable limits. This method was successfully employed in the pharmacokinetic study on rats after the oral administration of eriocitrin. The pharmacokinetic parameters show that the maximum plasma concentration ( ) of eriocitrin was 299.833 ± 16.743 μg L, while the corresponding time to reach ( ) was 0.094 ± 0.019 h, and the half-time ( ) was 1.752 ± 0.323 h. The present results would be valuable for further research and development of eriocitrin.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050387PMC
http://dx.doi.org/10.1039/c9ra10925kDOI Listing

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