Synthesis of hyaluronic acid or O-carboxymethyl chitosan-stabilized ZnO–ginsenoside Rh2 nanocomposites incorporated with aqueous leaf extract of Dendropanax morbifera Léveille: in vitro studies as potential sunscreen agents. (29th May 2019)
- Record Type:
- Journal Article
- Title:
- Synthesis of hyaluronic acid or O-carboxymethyl chitosan-stabilized ZnO–ginsenoside Rh2 nanocomposites incorporated with aqueous leaf extract of Dendropanax morbifera Léveille: in vitro studies as potential sunscreen agents. (29th May 2019)
- Main Title:
- Synthesis of hyaluronic acid or O-carboxymethyl chitosan-stabilized ZnO–ginsenoside Rh2 nanocomposites incorporated with aqueous leaf extract of Dendropanax morbifera Léveille: in vitro studies as potential sunscreen agents
- Authors:
- Markus, Josua
Mathiyalagan, Ramya
Kim, Yeon-Ju
Han, Yaxi
Jiménez-Pérez, Zuly Elizabeth
Veronika, Soshnikova
Yang, Deok-Chun - Abstract:
- Abstract : Synthesis of Rh2–ZnO nanocomposites stabilized with hyaluronic acid or O -carboxymethyl chitosan. Abstract : The present study elucidates the synthesis of hyaluronic acid (HA) or O -carboxymethyl chitosan (CMC)-stabilized zinc oxide nanocomposites (ZnONcs) incorporated with aqueous leaf extract of Dendropanax morbifera Léveille to enhance the water solubility of hydrophobic ginsenoside Rh2. Ginsenosides are triterpenoid saponins isolated from Panax ginseng and exhibit potent pharmacological effects and unique biological properties. The polymers were integrated to accommodate steric stabilization, provide terminal carboxylic groups for ginsenoside conjugation, and grant intrinsic clinical benefits for topical administrations. D. morbifera leaf extract was incorporated into the nanocomposites to enhance their antioxidant activities against DPPH and ABTS + radicals and water solubilization. Ginsenoside Rh2 was covalently conjugated via carbodiimide-intermediated esterification to form water-dispersible Rh2–HA–ZnONcs and Rh2–CMC–ZnONcs. Binding of ginsenoside Rh2 to ZnONcs was detected by FTIR and LC-MS. In vitro evaluation of ginsenoside-conjugated ZnONcs revealed that Rh2 conjugation increased the SPF rating and reduced the cytotoxicity in human keratinocyte (HaCaT) cells compared to unconjugated polymer-functionalized ZnONcs. Overall, Rh2–HA–ZnONcs and Rh2–CMC–ZnONcs show promising results as multi-functional carriers for ginsenoside Rh2 and can potentially beAbstract : Synthesis of Rh2–ZnO nanocomposites stabilized with hyaluronic acid or O -carboxymethyl chitosan. Abstract : The present study elucidates the synthesis of hyaluronic acid (HA) or O -carboxymethyl chitosan (CMC)-stabilized zinc oxide nanocomposites (ZnONcs) incorporated with aqueous leaf extract of Dendropanax morbifera Léveille to enhance the water solubility of hydrophobic ginsenoside Rh2. Ginsenosides are triterpenoid saponins isolated from Panax ginseng and exhibit potent pharmacological effects and unique biological properties. The polymers were integrated to accommodate steric stabilization, provide terminal carboxylic groups for ginsenoside conjugation, and grant intrinsic clinical benefits for topical administrations. D. morbifera leaf extract was incorporated into the nanocomposites to enhance their antioxidant activities against DPPH and ABTS + radicals and water solubilization. Ginsenoside Rh2 was covalently conjugated via carbodiimide-intermediated esterification to form water-dispersible Rh2–HA–ZnONcs and Rh2–CMC–ZnONcs. Binding of ginsenoside Rh2 to ZnONcs was detected by FTIR and LC-MS. In vitro evaluation of ginsenoside-conjugated ZnONcs revealed that Rh2 conjugation increased the SPF rating and reduced the cytotoxicity in human keratinocyte (HaCaT) cells compared to unconjugated polymer-functionalized ZnONcs. Overall, Rh2–HA–ZnONcs and Rh2–CMC–ZnONcs show promising results as multi-functional carriers for ginsenoside Rh2 and can potentially be implemented as novel bioactive sunscreen agents. … (more)
- Is Part Of:
- New journal of chemistry. Volume 43:Number 23(2019)
- Journal:
- New journal of chemistry
- Issue:
- Volume 43:Number 23(2019)
- Issue Display:
- Volume 43, Issue 23 (2019)
- Year:
- 2019
- Volume:
- 43
- Issue:
- 23
- Issue Sort Value:
- 2019-0043-0023-0000
- Page Start:
- 9188
- Page End:
- 9200
- Publication Date:
- 2019-05-29
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/c8nj06044d ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 10885.xml