Microemulsion-based hydrogels for enhancing epidermal/dermal deposition of topically administered 20(S)-protopanaxadiol: in vitro and in vivo evaluation studies

Background: 20(S)-Protopanaxadiol (20S-PPD) is a fully deglycosylated ginsenoside metabolite and has potent dermal antiaging activity. However, because of its low aqueous solubility and large molecular size, a suitable formulation strategy is required to improve its solubility and skin permeability,...

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Main Authors: Ki-Taek Kim, Min-Hwan Kim, Ju-Hwan Park, Jae-Young Lee, Hyun-Jong Cho, In-Soo Yoon, Dae-Duk Kim
Format: Article
Language:English
Published: Elsevier 2018-10-01
Series:Journal of Ginseng Research
Online Access:http://www.sciencedirect.com/science/article/pii/S122684531730115X
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spelling doaj-3a44bbefb0224123b5f44c39efd904eb2020-11-25T01:02:16ZengElsevierJournal of Ginseng Research1226-84532018-10-01424512523Microemulsion-based hydrogels for enhancing epidermal/dermal deposition of topically administered 20(S)-protopanaxadiol: in vitro and in vivo evaluation studiesKi-Taek Kim0Min-Hwan Kim1Ju-Hwan Park2Jae-Young Lee3Hyun-Jong Cho4In-Soo Yoon5Dae-Duk Kim6College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Republic of KoreaCollege of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Republic of KoreaCollege of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Republic of KoreaCollege of Pharmacy, Chungnam National University, Daejeon, Republic of KoreaCollege of Pharmacy, Kangwon National University, Gangwon, Republic of KoreaCollege of Pharmacy, Pusan National University, Busan, Republic of Korea; Corresponding author. College of Pharmacy, Pusan National University, 2 Busandaehak-ro 63 beon-gil, Geumjeong-gu, Busan 46241, Republic of Korea.College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Republic of Korea; Corresponding author. College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 08826, Republic of Korea.Background: 20(S)-Protopanaxadiol (20S-PPD) is a fully deglycosylated ginsenoside metabolite and has potent dermal antiaging activity. However, because of its low aqueous solubility and large molecular size, a suitable formulation strategy is required to improve its solubility and skin permeability, thereby enhancing its skin deposition. Thus, we optimized microemulsion (ME)-based hydrogel (MEH) formulations for the topical delivery of 20S-PPD. Methods: MEs and MEHs were formulated and evaluated for their particle size distribution, morphology, drug loading capacity, and stability. Then, the deposition profiles of the selected 20S-PPD-loaded MEH formulation were studied using a hairless mouse skin model and Strat-M membrane as an artificial skin model. Results: A Carbopol-based MEH system of 20S-PPD was successfully prepared with a mean droplet size of 110 nm and narrow size distribution. The formulation was stable for 56 d, and its viscosity was high enough for its topical application. It significantly enhanced the in vitro and in vivo skin deposition of 20S-PPD with no influence on its systemic absorption in hairless mice. Notably, it was found that the Strat-M membrane provided skin deposition data well correlated to those obtained from the in vitro and in vivo mouse skin studies on 20S-PPD (correlation coefficient r2 = 0.929‒0.947). Conclusion: The MEH formulation developed in this study could serve as an effective topical delivery system for poorly soluble ginsenosides and their deglycosylated metabolites, including 20S-PPD. Keywords: hairless mouse, microemulsion-based hydrogel (MEH), 20(S)-protopanaxadiol (20S-PPD), Strat-M membrane, topical deliveryhttp://www.sciencedirect.com/science/article/pii/S122684531730115X
collection DOAJ
language English
format Article
sources DOAJ
author Ki-Taek Kim
Min-Hwan Kim
Ju-Hwan Park
Jae-Young Lee
Hyun-Jong Cho
In-Soo Yoon
Dae-Duk Kim
spellingShingle Ki-Taek Kim
Min-Hwan Kim
Ju-Hwan Park
Jae-Young Lee
Hyun-Jong Cho
In-Soo Yoon
Dae-Duk Kim
Microemulsion-based hydrogels for enhancing epidermal/dermal deposition of topically administered 20(S)-protopanaxadiol: in vitro and in vivo evaluation studies
Journal of Ginseng Research
author_facet Ki-Taek Kim
Min-Hwan Kim
Ju-Hwan Park
Jae-Young Lee
Hyun-Jong Cho
In-Soo Yoon
Dae-Duk Kim
author_sort Ki-Taek Kim
title Microemulsion-based hydrogels for enhancing epidermal/dermal deposition of topically administered 20(S)-protopanaxadiol: in vitro and in vivo evaluation studies
title_short Microemulsion-based hydrogels for enhancing epidermal/dermal deposition of topically administered 20(S)-protopanaxadiol: in vitro and in vivo evaluation studies
title_full Microemulsion-based hydrogels for enhancing epidermal/dermal deposition of topically administered 20(S)-protopanaxadiol: in vitro and in vivo evaluation studies
title_fullStr Microemulsion-based hydrogels for enhancing epidermal/dermal deposition of topically administered 20(S)-protopanaxadiol: in vitro and in vivo evaluation studies
title_full_unstemmed Microemulsion-based hydrogels for enhancing epidermal/dermal deposition of topically administered 20(S)-protopanaxadiol: in vitro and in vivo evaluation studies
title_sort microemulsion-based hydrogels for enhancing epidermal/dermal deposition of topically administered 20(s)-protopanaxadiol: in vitro and in vivo evaluation studies
publisher Elsevier
series Journal of Ginseng Research
issn 1226-8453
publishDate 2018-10-01
description Background: 20(S)-Protopanaxadiol (20S-PPD) is a fully deglycosylated ginsenoside metabolite and has potent dermal antiaging activity. However, because of its low aqueous solubility and large molecular size, a suitable formulation strategy is required to improve its solubility and skin permeability, thereby enhancing its skin deposition. Thus, we optimized microemulsion (ME)-based hydrogel (MEH) formulations for the topical delivery of 20S-PPD. Methods: MEs and MEHs were formulated and evaluated for their particle size distribution, morphology, drug loading capacity, and stability. Then, the deposition profiles of the selected 20S-PPD-loaded MEH formulation were studied using a hairless mouse skin model and Strat-M membrane as an artificial skin model. Results: A Carbopol-based MEH system of 20S-PPD was successfully prepared with a mean droplet size of 110 nm and narrow size distribution. The formulation was stable for 56 d, and its viscosity was high enough for its topical application. It significantly enhanced the in vitro and in vivo skin deposition of 20S-PPD with no influence on its systemic absorption in hairless mice. Notably, it was found that the Strat-M membrane provided skin deposition data well correlated to those obtained from the in vitro and in vivo mouse skin studies on 20S-PPD (correlation coefficient r2 = 0.929‒0.947). Conclusion: The MEH formulation developed in this study could serve as an effective topical delivery system for poorly soluble ginsenosides and their deglycosylated metabolites, including 20S-PPD. Keywords: hairless mouse, microemulsion-based hydrogel (MEH), 20(S)-protopanaxadiol (20S-PPD), Strat-M membrane, topical delivery
url http://www.sciencedirect.com/science/article/pii/S122684531730115X
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