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The development and validation of an HPLC-MS/MS method for the determination of eriocitrin in rat plasma and its application to a pharmacokinetic study

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 chromato...

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Autores principales: Li, Luya, Feng, Rui, Feng, Xue, Chen, Yuting, Liu, Xin, Sun, Wenjing, Zhang, Lantong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050387/
https://www.ncbi.nlm.nih.gov/pubmed/35492908
http://dx.doi.org/10.1039/c9ra10925k
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author Li, Luya
Feng, Rui
Feng, Xue
Chen, Yuting
Liu, Xin
Sun, Wenjing
Zhang, Lantong
author_facet Li, Luya
Feng, Rui
Feng, Xue
Chen, Yuting
Liu, Xin
Sun, Wenjing
Zhang, Lantong
author_sort Li, Luya
collection PubMed
description 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(−1). In multiple reaction monitoring (MRM) modes, eriocitrin and internal standard (IS) were quantified using precursor-to-product ion transitions of m/z 595.4 → 287.1 and m/z 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 (C(max)) of eriocitrin was 299.833 ± 16.743 μg L(−1), while the corresponding time to reach C(max)(T(max)) was 0.094 ± 0.019 h, and the half-time (T(1/2)) was 1.752 ± 0.323 h. The present results would be valuable for further research and development of eriocitrin.
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spelling pubmed-90503872022-04-29 The development and validation of an HPLC-MS/MS method for the determination of eriocitrin in rat plasma and its application to a pharmacokinetic study Li, Luya Feng, Rui Feng, Xue Chen, Yuting Liu, Xin Sun, Wenjing Zhang, Lantong RSC Adv Chemistry 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(−1). In multiple reaction monitoring (MRM) modes, eriocitrin and internal standard (IS) were quantified using precursor-to-product ion transitions of m/z 595.4 → 287.1 and m/z 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 (C(max)) of eriocitrin was 299.833 ± 16.743 μg L(−1), while the corresponding time to reach C(max)(T(max)) was 0.094 ± 0.019 h, and the half-time (T(1/2)) was 1.752 ± 0.323 h. The present results would be valuable for further research and development of eriocitrin. The Royal Society of Chemistry 2020-03-12 /pmc/articles/PMC9050387/ /pubmed/35492908 http://dx.doi.org/10.1039/c9ra10925k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Li, Luya
Feng, Rui
Feng, Xue
Chen, Yuting
Liu, Xin
Sun, Wenjing
Zhang, Lantong
The development and validation of an HPLC-MS/MS method for the determination of eriocitrin in rat plasma and its application to a pharmacokinetic study
title The development and validation of an HPLC-MS/MS method for the determination of eriocitrin in rat plasma and its application to a pharmacokinetic study
title_full The development and validation of an HPLC-MS/MS method for the determination of eriocitrin in rat plasma and its application to a pharmacokinetic study
title_fullStr The development and validation of an HPLC-MS/MS method for the determination of eriocitrin in rat plasma and its application to a pharmacokinetic study
title_full_unstemmed The development and validation of an HPLC-MS/MS method for the determination of eriocitrin in rat plasma and its application to a pharmacokinetic study
title_short The development and validation of an HPLC-MS/MS method for the determination of eriocitrin in rat plasma and its application to a pharmacokinetic study
title_sort development and validation of an hplc-ms/ms method for the determination of eriocitrin in rat plasma and its application to a pharmacokinetic study
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050387/
https://www.ncbi.nlm.nih.gov/pubmed/35492908
http://dx.doi.org/10.1039/c9ra10925k
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