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Toxicokinetics of 11 Gelsemium Alkaloids in Rats by UPLC-MS/MS

Gelsemium elegans (Gardn. & Champ.) Benth. is a plant belonging to the genus Gelsemium (family Gelsemiaceae), and its main components are alkaloids. It is a Chinese traditional medicinal plant and notoriously known as a highly toxic medicine. However, a method has not yet been found for the simu...

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Autores principales: Shen, Xiuwei, Ma, Jianshe, Wang, Xianqin, Wen, Congcong, Zhang, Meiling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378607/
https://www.ncbi.nlm.nih.gov/pubmed/32733957
http://dx.doi.org/10.1155/2020/8247270
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author Shen, Xiuwei
Ma, Jianshe
Wang, Xianqin
Wen, Congcong
Zhang, Meiling
author_facet Shen, Xiuwei
Ma, Jianshe
Wang, Xianqin
Wen, Congcong
Zhang, Meiling
author_sort Shen, Xiuwei
collection PubMed
description Gelsemium elegans (Gardn. & Champ.) Benth. is a plant belonging to the genus Gelsemium (family Gelsemiaceae), and its main components are alkaloids. It is a Chinese traditional medicinal plant and notoriously known as a highly toxic medicine. However, a method has not yet been found for the simultaneous detection of 11 Gelsemium alkaloids in rat plasma, and the toxicokinetics of 11 Gelsemium alkaloids after intravenous administration has not been reported. In this work, we have developed a sensitive and rapid method of ultraperformance liquid chromatography/tandem mass spectrometry (UPLC-MS/MS) for the detection of 11 Gelsemium alkaloids in rat plasma. The toxicokinetic behavior was also investigated, so as to provide a reference of the scientific properties of Gelsemium elegans and improve the efficacy and safety of drugs. Sixty-six Sprague-Dawley rats were randomly divided into 11 groups, six rats in each group. Each group was intravenously given one alkaloid (0.1 mg/kg), respectively. A Waters UPLC BEH C18 column (50 mm × 2.1 mm, 1.7 μm) was used for chromatographic separation. Methanol and water (containing 0.1% formic acid) were used for the mobile phase with gradient elution. Multiple reactions were monitored, and positive electrospray ionization was used for quantitative analysis. The precision was less than 16%, and the accuracy was between 86.9% and 113.2%. The extraction efficiency was better than 75.8%, and the matrix effects ranged from 88.5% to 107.8%. The calibration curves were in the range of 0.1–200 ng/mL, with a correlation coefficient (R(2)) greater than 0.995. The UPLC-MS/MS method was successfully applied to the toxicokinetics of 11 Gelsemium alkaloids in rats after intravenous administration (0.1 mg/kg for each alkaloid). The results of the toxicokinetics provide a basis for the pharmacology and toxicology of Gelsemium alkaloids and scientific evidence for the clinical use of Gelsemium alkaloids.
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spelling pubmed-73786072020-07-29 Toxicokinetics of 11 Gelsemium Alkaloids in Rats by UPLC-MS/MS Shen, Xiuwei Ma, Jianshe Wang, Xianqin Wen, Congcong Zhang, Meiling Biomed Res Int Research Article Gelsemium elegans (Gardn. & Champ.) Benth. is a plant belonging to the genus Gelsemium (family Gelsemiaceae), and its main components are alkaloids. It is a Chinese traditional medicinal plant and notoriously known as a highly toxic medicine. However, a method has not yet been found for the simultaneous detection of 11 Gelsemium alkaloids in rat plasma, and the toxicokinetics of 11 Gelsemium alkaloids after intravenous administration has not been reported. In this work, we have developed a sensitive and rapid method of ultraperformance liquid chromatography/tandem mass spectrometry (UPLC-MS/MS) for the detection of 11 Gelsemium alkaloids in rat plasma. The toxicokinetic behavior was also investigated, so as to provide a reference of the scientific properties of Gelsemium elegans and improve the efficacy and safety of drugs. Sixty-six Sprague-Dawley rats were randomly divided into 11 groups, six rats in each group. Each group was intravenously given one alkaloid (0.1 mg/kg), respectively. A Waters UPLC BEH C18 column (50 mm × 2.1 mm, 1.7 μm) was used for chromatographic separation. Methanol and water (containing 0.1% formic acid) were used for the mobile phase with gradient elution. Multiple reactions were monitored, and positive electrospray ionization was used for quantitative analysis. The precision was less than 16%, and the accuracy was between 86.9% and 113.2%. The extraction efficiency was better than 75.8%, and the matrix effects ranged from 88.5% to 107.8%. The calibration curves were in the range of 0.1–200 ng/mL, with a correlation coefficient (R(2)) greater than 0.995. The UPLC-MS/MS method was successfully applied to the toxicokinetics of 11 Gelsemium alkaloids in rats after intravenous administration (0.1 mg/kg for each alkaloid). The results of the toxicokinetics provide a basis for the pharmacology and toxicology of Gelsemium alkaloids and scientific evidence for the clinical use of Gelsemium alkaloids. Hindawi 2020-07-15 /pmc/articles/PMC7378607/ /pubmed/32733957 http://dx.doi.org/10.1155/2020/8247270 Text en Copyright © 2020 Xiuwei Shen et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Shen, Xiuwei
Ma, Jianshe
Wang, Xianqin
Wen, Congcong
Zhang, Meiling
Toxicokinetics of 11 Gelsemium Alkaloids in Rats by UPLC-MS/MS
title Toxicokinetics of 11 Gelsemium Alkaloids in Rats by UPLC-MS/MS
title_full Toxicokinetics of 11 Gelsemium Alkaloids in Rats by UPLC-MS/MS
title_fullStr Toxicokinetics of 11 Gelsemium Alkaloids in Rats by UPLC-MS/MS
title_full_unstemmed Toxicokinetics of 11 Gelsemium Alkaloids in Rats by UPLC-MS/MS
title_short Toxicokinetics of 11 Gelsemium Alkaloids in Rats by UPLC-MS/MS
title_sort toxicokinetics of 11 gelsemium alkaloids in rats by uplc-ms/ms
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7378607/
https://www.ncbi.nlm.nih.gov/pubmed/32733957
http://dx.doi.org/10.1155/2020/8247270
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