Bioconversion of BIOGF1K, a compound-K-rich fraction from ginseng root and its effect on epidermal barrier function

Woo-Hyun Kim; Jeong-Eun Kim; Sehyun Kim; Yongjoo Na; Yong-Deok Hong; Joonho Choi; Won-Seok Park; Soon-Mi Shim

doi:10.1016/j.heliyon.2023.e14803

Bioconversion of BIOGF1K, a compound-K-rich fraction from ginseng root and its effect on epidermal barrier function

Heliyon. 2023 Mar 22;9(4):e14803. doi: 10.1016/j.heliyon.2023.e14803. eCollection 2023 Apr.

Authors

Woo-Hyun Kim¹, Jeong-Eun Kim¹, Sehyun Kim², Yongjoo Na², Yong-Deok Hong², Joonho Choi², Won-Seok Park², Soon-Mi Shim¹

Affiliations

¹ Department of Food Science and Biotechnology, Sejong University, 98 Gunja-dong, Seoul 05006, South Korea.
² AMOREPACIFIC Research and Innovation Center, 1920, Yonggu-daero, Giheung-gu, Yongin-si 17074, Gyeonggi-do, South Korea.

Abstract

BIOGF1K, the ginseng root-based and hydrolyzed ginsenoside-rich fraction, is known to improve skin damage, but there are rare studies on the kinetic of ginsenosides in the epidermis and their effects on epidermal barrier function. The current study investigated the effect of BIOGF1K on epidermal barrier function and its kinetics on epidermal transport. HPLC and LC/MS were used to verify the ginsenosides and the metabolites of BIOGF1K. Human immortalized keratinocytes (HaCaT) and epidermis-dermis artificial skin were treated with BIOGF1K and their metabolites were analyzed by HPLC and LC/MS. The epidermal barrier function was evaluated by transepithelial electrical resistance (TEER). In BIOGF1K, ginsenoside Rg1, Rd, F1, F2, compound Mc, compound Y (CY), and compound K (CK) were detected and CK and CY were the most and second abundant ginsenosides. TEER of HaCaT with 100 and 200 μg/mL BIOGF1K treatment was significantly higher than the control during 600 min of incubation. CK was permeated to the epidermis in a time-dependent manner and its maximum transported rate was observed at 600 min. In the case of artificial skin, CY and CK were permeated to the epidermis-dermis skin as time-dependent. Also, 24 h after treatment of CY, CK was detected as 19.59% of CY. It was proposed that CY was hydrolyzed into CK while permeating the epidermis. Results from the current study suggest that bioconversion of BIOGF1K rich in CK effectively enhances epidermal barrier function and it could be a useful cosmeceutical to exhibit its functionality to the skin.

Keywords: Artificial skin; Barrier function; Epidermal transport; Ginsenoside compound K; HaCaT.