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Kinetic conversion of BIOGF1K enriched in compound K from in vitro 3-D human tissue model

The purposes of current study were to investigate the effect of ginsenosides from BIOGF1K enriched in compound K (CK) and compound Y (CY) on the skin barrier function, the deposition in in vitro 3-D human tissue model (EpiDermFT™ Full Thickness 400), and to identify and quantify kinetic bioconversio...

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Autores principales: Kim, Woo-Hyun, Choi, Won-Jo, Kim, Jeong-Eun, Choi, Joonho, Hong, Yong-Deok, Nam, Jin, Park, Won-Seok, Shim, Soon-Mi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10589745/
https://www.ncbi.nlm.nih.gov/pubmed/37869704
http://dx.doi.org/10.1016/j.crphar.2023.100165
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author Kim, Woo-Hyun
Choi, Won-Jo
Kim, Jeong-Eun
Choi, Joonho
Hong, Yong-Deok
Nam, Jin
Park, Won-Seok
Shim, Soon-Mi
author_facet Kim, Woo-Hyun
Choi, Won-Jo
Kim, Jeong-Eun
Choi, Joonho
Hong, Yong-Deok
Nam, Jin
Park, Won-Seok
Shim, Soon-Mi
author_sort Kim, Woo-Hyun
collection PubMed
description The purposes of current study were to investigate the effect of ginsenosides from BIOGF1K enriched in compound K (CK) and compound Y (CY) on the skin barrier function, the deposition in in vitro 3-D human tissue model (EpiDermFT™ Full Thickness 400), and to identify and quantify kinetic bioconversion of the ginsenosides in artificial skin by utilizing the Fourier transform infrared spectroscopy (FT-IR) and liquid chromatography mass spectrometry (LC-MS), respectively. Epidermal barrier integrity evaluated using transepithelial electrical resistance (TEER) was significantly higher in the BIOGF1K treatment than the CY or CK individual treatment throughout incubation (p < 0.05). Skin deposition (%) of CY and CK from BIOGF1K treatment was approximately 4 and 2 times higher than the CY and CK single component treatment, respectively. Total amount of CK found in human skin by deposition and bioconversion was approximately 1087.3, 528.82, and 867.76 μM after topical treatment of BIOGF1K, CK, and CY. Results from the current study reveal that topical treatment of BIOGF1K more effectively induced CK deposition as well as bioconversion of CY to CK than that of a single treatment of CY or CK, suggesting that BIOGF1K could be a useful cosmetic preparation for enhancing skin function.
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spelling pubmed-105897452023-10-22 Kinetic conversion of BIOGF1K enriched in compound K from in vitro 3-D human tissue model Kim, Woo-Hyun Choi, Won-Jo Kim, Jeong-Eun Choi, Joonho Hong, Yong-Deok Nam, Jin Park, Won-Seok Shim, Soon-Mi Curr Res Pharmacol Drug Discov Article The purposes of current study were to investigate the effect of ginsenosides from BIOGF1K enriched in compound K (CK) and compound Y (CY) on the skin barrier function, the deposition in in vitro 3-D human tissue model (EpiDermFT™ Full Thickness 400), and to identify and quantify kinetic bioconversion of the ginsenosides in artificial skin by utilizing the Fourier transform infrared spectroscopy (FT-IR) and liquid chromatography mass spectrometry (LC-MS), respectively. Epidermal barrier integrity evaluated using transepithelial electrical resistance (TEER) was significantly higher in the BIOGF1K treatment than the CY or CK individual treatment throughout incubation (p < 0.05). Skin deposition (%) of CY and CK from BIOGF1K treatment was approximately 4 and 2 times higher than the CY and CK single component treatment, respectively. Total amount of CK found in human skin by deposition and bioconversion was approximately 1087.3, 528.82, and 867.76 μM after topical treatment of BIOGF1K, CK, and CY. Results from the current study reveal that topical treatment of BIOGF1K more effectively induced CK deposition as well as bioconversion of CY to CK than that of a single treatment of CY or CK, suggesting that BIOGF1K could be a useful cosmetic preparation for enhancing skin function. Elsevier 2023-10-12 /pmc/articles/PMC10589745/ /pubmed/37869704 http://dx.doi.org/10.1016/j.crphar.2023.100165 Text en © 2023 Published by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Kim, Woo-Hyun
Choi, Won-Jo
Kim, Jeong-Eun
Choi, Joonho
Hong, Yong-Deok
Nam, Jin
Park, Won-Seok
Shim, Soon-Mi
Kinetic conversion of BIOGF1K enriched in compound K from in vitro 3-D human tissue model
title Kinetic conversion of BIOGF1K enriched in compound K from in vitro 3-D human tissue model
title_full Kinetic conversion of BIOGF1K enriched in compound K from in vitro 3-D human tissue model
title_fullStr Kinetic conversion of BIOGF1K enriched in compound K from in vitro 3-D human tissue model
title_full_unstemmed Kinetic conversion of BIOGF1K enriched in compound K from in vitro 3-D human tissue model
title_short Kinetic conversion of BIOGF1K enriched in compound K from in vitro 3-D human tissue model
title_sort kinetic conversion of biogf1k enriched in compound k from in vitro 3-d human tissue model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10589745/
https://www.ncbi.nlm.nih.gov/pubmed/37869704
http://dx.doi.org/10.1016/j.crphar.2023.100165
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