Cargando…

Intra-Herb Interactions: Primary Metabolites in Coptidis Rhizoma Extract Improved the Pharmacokinetics of Oral Berberine Hydrochloride in Mice

Primary plant metabolites can be used for artificial preparation of natural deep eutectic solvents (NADESs), which have strong dissolving capacity, good biocompatibility, and biodegradability. In this study, for the first time, we verified that NADESs were present in Coptidis Rhizoma extract and sys...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Jing, Zhou, Ting, Lu, Jing-Ze, Ye, Dan, Mu, Sheng, Tian, Xin-Hui, Zhang, Wei-Dong, Ma, Bing-Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8215677/
https://www.ncbi.nlm.nih.gov/pubmed/34163360
http://dx.doi.org/10.3389/fphar.2021.675368
_version_ 1783710288690806784
author Zhao, Jing
Zhou, Ting
Lu, Jing-Ze
Ye, Dan
Mu, Sheng
Tian, Xin-Hui
Zhang, Wei-Dong
Ma, Bing-Liang
author_facet Zhao, Jing
Zhou, Ting
Lu, Jing-Ze
Ye, Dan
Mu, Sheng
Tian, Xin-Hui
Zhang, Wei-Dong
Ma, Bing-Liang
author_sort Zhao, Jing
collection PubMed
description Primary plant metabolites can be used for artificial preparation of natural deep eutectic solvents (NADESs), which have strong dissolving capacity, good biocompatibility, and biodegradability. In this study, for the first time, we verified that NADESs were present in Coptidis Rhizoma extract and systematically investigated its effects and mechanisms on the pharmacokinetics of oral berberine hydrochloride (BBR), a co-existing bioactive constituent. First, three LC-MS/MS based methods were established and fully validated to determine the levels of 11 primary metabolites in Coptidis Rhizoma extract. According to the weight ratio of four major primary metabolites in the Coptidis Rhizoma extract, a stable “endogenous” NADES was prepared using the heating method by the addition of 350 μl of water to 1,307.8 mg of the mixture of malic acid (490.5 mg), glucose (280.6 mg), sucrose (517.7 mg), and choline chloride (19.0 mg). The prepared NADES showed significant acute toxicity in mice and cytotoxicity in MDCK-MDR1 cells. However, after being diluted 10 times or 100 times, the NADES had no significant acute toxicity or cytotoxicity, respectively. The dilutions of the NADES significantly increased the water solubility of BBR, reduced its efflux in gut sacs and MDCK-MDR1 cell monolayer, and improved its metabolic stability in intestinal S9. In addition, the NADES dilutions reversibly opened the tight junctions between the enterocytes in the gut sacs. Moreover, the NADES dilutions significantly improved the exposure levels of BBR in the portal vein and livers of mice that were administered oral BBR. Malic acid was identified as a major component in the NADES in terms of solubility, acute toxicity, cytotoxicity, and pharmacokinetic-improving effects on oral BBR. In conclusion, the primary metabolites of Coptidis Rhizoma extract could form “endogenous” NADES, and its dilutions improve the pharmacokinetics of oral BBR. This study demonstrates the synergistic interaction of the constituents of Coptidis Rhizoma extract and the potential use of the NADES dilutions in oral BBR delivery.
format Online
Article
Text
id pubmed-8215677
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-82156772021-06-22 Intra-Herb Interactions: Primary Metabolites in Coptidis Rhizoma Extract Improved the Pharmacokinetics of Oral Berberine Hydrochloride in Mice Zhao, Jing Zhou, Ting Lu, Jing-Ze Ye, Dan Mu, Sheng Tian, Xin-Hui Zhang, Wei-Dong Ma, Bing-Liang Front Pharmacol Pharmacology Primary plant metabolites can be used for artificial preparation of natural deep eutectic solvents (NADESs), which have strong dissolving capacity, good biocompatibility, and biodegradability. In this study, for the first time, we verified that NADESs were present in Coptidis Rhizoma extract and systematically investigated its effects and mechanisms on the pharmacokinetics of oral berberine hydrochloride (BBR), a co-existing bioactive constituent. First, three LC-MS/MS based methods were established and fully validated to determine the levels of 11 primary metabolites in Coptidis Rhizoma extract. According to the weight ratio of four major primary metabolites in the Coptidis Rhizoma extract, a stable “endogenous” NADES was prepared using the heating method by the addition of 350 μl of water to 1,307.8 mg of the mixture of malic acid (490.5 mg), glucose (280.6 mg), sucrose (517.7 mg), and choline chloride (19.0 mg). The prepared NADES showed significant acute toxicity in mice and cytotoxicity in MDCK-MDR1 cells. However, after being diluted 10 times or 100 times, the NADES had no significant acute toxicity or cytotoxicity, respectively. The dilutions of the NADES significantly increased the water solubility of BBR, reduced its efflux in gut sacs and MDCK-MDR1 cell monolayer, and improved its metabolic stability in intestinal S9. In addition, the NADES dilutions reversibly opened the tight junctions between the enterocytes in the gut sacs. Moreover, the NADES dilutions significantly improved the exposure levels of BBR in the portal vein and livers of mice that were administered oral BBR. Malic acid was identified as a major component in the NADES in terms of solubility, acute toxicity, cytotoxicity, and pharmacokinetic-improving effects on oral BBR. In conclusion, the primary metabolites of Coptidis Rhizoma extract could form “endogenous” NADES, and its dilutions improve the pharmacokinetics of oral BBR. This study demonstrates the synergistic interaction of the constituents of Coptidis Rhizoma extract and the potential use of the NADES dilutions in oral BBR delivery. Frontiers Media S.A. 2021-06-07 /pmc/articles/PMC8215677/ /pubmed/34163360 http://dx.doi.org/10.3389/fphar.2021.675368 Text en Copyright © 2021 Zhao, Zhou, Lu, Ye, Mu, Tian, Zhang and Ma. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Zhao, Jing
Zhou, Ting
Lu, Jing-Ze
Ye, Dan
Mu, Sheng
Tian, Xin-Hui
Zhang, Wei-Dong
Ma, Bing-Liang
Intra-Herb Interactions: Primary Metabolites in Coptidis Rhizoma Extract Improved the Pharmacokinetics of Oral Berberine Hydrochloride in Mice
title Intra-Herb Interactions: Primary Metabolites in Coptidis Rhizoma Extract Improved the Pharmacokinetics of Oral Berberine Hydrochloride in Mice
title_full Intra-Herb Interactions: Primary Metabolites in Coptidis Rhizoma Extract Improved the Pharmacokinetics of Oral Berberine Hydrochloride in Mice
title_fullStr Intra-Herb Interactions: Primary Metabolites in Coptidis Rhizoma Extract Improved the Pharmacokinetics of Oral Berberine Hydrochloride in Mice
title_full_unstemmed Intra-Herb Interactions: Primary Metabolites in Coptidis Rhizoma Extract Improved the Pharmacokinetics of Oral Berberine Hydrochloride in Mice
title_short Intra-Herb Interactions: Primary Metabolites in Coptidis Rhizoma Extract Improved the Pharmacokinetics of Oral Berberine Hydrochloride in Mice
title_sort intra-herb interactions: primary metabolites in coptidis rhizoma extract improved the pharmacokinetics of oral berberine hydrochloride in mice
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8215677/
https://www.ncbi.nlm.nih.gov/pubmed/34163360
http://dx.doi.org/10.3389/fphar.2021.675368
work_keys_str_mv AT zhaojing intraherbinteractionsprimarymetabolitesincoptidisrhizomaextractimprovedthepharmacokineticsoforalberberinehydrochlorideinmice
AT zhouting intraherbinteractionsprimarymetabolitesincoptidisrhizomaextractimprovedthepharmacokineticsoforalberberinehydrochlorideinmice
AT lujingze intraherbinteractionsprimarymetabolitesincoptidisrhizomaextractimprovedthepharmacokineticsoforalberberinehydrochlorideinmice
AT yedan intraherbinteractionsprimarymetabolitesincoptidisrhizomaextractimprovedthepharmacokineticsoforalberberinehydrochlorideinmice
AT musheng intraherbinteractionsprimarymetabolitesincoptidisrhizomaextractimprovedthepharmacokineticsoforalberberinehydrochlorideinmice
AT tianxinhui intraherbinteractionsprimarymetabolitesincoptidisrhizomaextractimprovedthepharmacokineticsoforalberberinehydrochlorideinmice
AT zhangweidong intraherbinteractionsprimarymetabolitesincoptidisrhizomaextractimprovedthepharmacokineticsoforalberberinehydrochlorideinmice
AT mabingliang intraherbinteractionsprimarymetabolitesincoptidisrhizomaextractimprovedthepharmacokineticsoforalberberinehydrochlorideinmice