Biodistribution and pharmacokinetic evaluation of Korean Red Ginseng components using radioisotopes in a rat model.

Autoradiography Ginsenosides Korean Red Ginseng Pharmacokinetics Radioisotopes

Journal

Journal of ginseng research
ISSN: 1226-8453
Titre abrégé: J Ginseng Res
Pays: Korea (South)
ID NLM: 100890690

Informations de publication

Date de publication:
Jan 2023
Historique:
received: 29 10 2021
revised: 15 03 2022
accepted: 02 05 2022
entrez: 16 1 2023
pubmed: 17 1 2023
medline: 17 1 2023
Statut: ppublish

Résumé

Although many studies have evaluated the efficacy and pharmacokinetics of Korean Red Ginseng (KRG) components (Rg1, Rb1, Rg3, Rd, etc.), few have examined the in vivo pharmacokinetics of the radiolabeled components. This study investigated the pharmacokinetics of ginsenosides and their metabolite compound K (CK), 20(s)-protopanaxadiol (PPD), and 20(s)-protopanaxatriol (PPT) using radioisotopes in rat oral administration. Sprague-Dawley rats were dosed orally once with 10 mg/kg of the tritium(3H) radiolabeled samples, and then the blood was collected from the tail vein after 0.25, 0.5, 1, 1.5, 2, 4, 6, 8, 12, 24, 48, 96, and 168 h. Radioactivity in the organs, feces, urine, and carcass was determined using a liquid scintillation counter (LSC) and a bio-imaging analyzer system (BAS). After oral administration, as the

Sections du résumé

Background UNASSIGNED
Although many studies have evaluated the efficacy and pharmacokinetics of Korean Red Ginseng (KRG) components (Rg1, Rb1, Rg3, Rd, etc.), few have examined the in vivo pharmacokinetics of the radiolabeled components. This study investigated the pharmacokinetics of ginsenosides and their metabolite compound K (CK), 20(s)-protopanaxadiol (PPD), and 20(s)-protopanaxatriol (PPT) using radioisotopes in rat oral administration.
Methods UNASSIGNED
Sprague-Dawley rats were dosed orally once with 10 mg/kg of the tritium(3H) radiolabeled samples, and then the blood was collected from the tail vein after 0.25, 0.5, 1, 1.5, 2, 4, 6, 8, 12, 24, 48, 96, and 168 h. Radioactivity in the organs, feces, urine, and carcass was determined using a liquid scintillation counter (LSC) and a bio-imaging analyzer system (BAS).
Results and conclusion UNASSIGNED
After oral administration, as the

Identifiants

pubmed: 36644381
doi: 10.1016/j.jgr.2022.05.001
pii: S1226-8453(22)00060-4
pmc: PMC9834004
doi:

Types de publication

Journal Article

Langues

eng

Pagination

74-80

Informations de copyright

© 2022 The Korean Society of Ginseng. Publishing services by Elsevier B.V.

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Sung-Won Kim (SW)

Laboratory of Efficacy Research, Korea Ginseng Corporation, Daejeon, Republic of Korea.

Byung-Cheol Han (BC)

Laboratory of Efficacy Research, Korea Ginseng Corporation, Daejeon, Republic of Korea.

Seung-Ho So (SH)

Laboratory of Efficacy Research, Korea Ginseng Corporation, Daejeon, Republic of Korea.

Chang-Kyun Han (CK)

Laboratory of Efficacy Research, Korea Ginseng Corporation, Daejeon, Republic of Korea.

Gyo In (G)

Laboratory of Efficacy Research, Korea Ginseng Corporation, Daejeon, Republic of Korea.

Chae-Kyu Park (CK)

Laboratory of Efficacy Research, Korea Ginseng Corporation, Daejeon, Republic of Korea.

Sun Hee Hyun (SH)

Laboratory of Efficacy Research, Korea Ginseng Corporation, Daejeon, Republic of Korea.

Classifications MeSH