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

Q2 Agricultural and Biological Sciences Current Research in Pharmacology and Drug Discovery Pub Date : 2023-01-01 DOI:10.1016/j.crphar.2023.100165
Woo-Hyun Kim , Won-Jo Choi , Jeong-Eun Kim , Joonho Choi , Yong-Deok Hong , Jin Nam , Won-Seok Park , Soon-Mi Shim
{"title":"Kinetic conversion of BIOGF1K enriched in compound K from in vitro 3-D human tissue model","authors":"Woo-Hyun Kim ,&nbsp;Won-Jo Choi ,&nbsp;Jeong-Eun Kim ,&nbsp;Joonho Choi ,&nbsp;Yong-Deok Hong ,&nbsp;Jin Nam ,&nbsp;Won-Seok Park ,&nbsp;Soon-Mi Shim","doi":"10.1016/j.crphar.2023.100165","DOIUrl":null,"url":null,"abstract":"<div><p>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 <em>in vitro</em> 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 &lt; 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.</p></div>","PeriodicalId":10877,"journal":{"name":"Current Research in Pharmacology and Drug Discovery","volume":"5 ","pages":"Article 100165"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Research in Pharmacology and Drug Discovery","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590257123000135","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Agricultural and Biological Sciences","Score":null,"Total":0}
引用次数: 0

Abstract

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.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
从体外三维人体组织模型中富集化合物K的BIOGF1K的动力学转化
本研究的目的是研究富含化合物K(CK)和化合物Y(CY)的BIOGF1K中的人参皂苷对皮肤屏障功能、体外三维人体组织模型(EpiDermFT™ Full Thickness 400),并分别利用傅立叶变换红外光谱(FT-IR)和液相色谱-质谱(LC-MS)鉴定和定量人工皮肤中人参皂苷的动力学生物转化。在整个培养过程中,使用跨上皮电阻(TEER)评估的表皮屏障完整性在BIOGF1K处理中显著高于CY或CK单独处理(p<0.05)。BIOGF1K处理的CY和CK的皮肤沉积(%)分别是CY和CK单组分处理的约4倍和2倍。局部处理BIOGF1K、CK和CY后,通过沉积和生物转化在人类皮肤中发现的CK总量约为1087.3、528.82和867.76μM。当前研究的结果表明,局部处理BIOGF1K比单独处理CY或CK更有效地诱导CK沉积和CY向CK的生物转化,表明BIOGF1K可能是一种有用的增强皮肤功能的化妆品制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Current Research in Pharmacology and Drug Discovery
Current Research in Pharmacology and Drug Discovery Agricultural and Biological Sciences-Animal Science and Zoology
CiteScore
6.40
自引率
0.00%
发文量
65
审稿时长
40 days
期刊最新文献
Editorial Board Table of Contents Development of Recombinant Antibody by Yeast Surface Display Technology Papaverine attenuates the progression of alpha naphthylisothiocyanate induce cholestasis in rats Long-term effects of neonatal pain and sucrose treatment
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1