Preparation and Evaluation of Liposomes and Niosomes Containing Total Ginsenosides for Anti-Photoaging Therapy

Ginsenosides are the principal bioactive compounds of ginseng. Total ginsenosides (GS) contain a variety of saponin monomers, which have potent anti-photoaging activity and improve the skin barrier function. To enhance the efficiency of GS transdermal absorption, GS liposomes (GSLs) and GS niosomes...

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Bibliographic Details
Main Authors: Chen, J. (Author), Jin, Y. (Author), Liu, D. (Author), Lu, Z. (Author), Qiu, Z. (Author), Yang, L. (Author), Zhou, X. (Author)
Format: Article
Language:English
Published: Frontiers Media S.A. 2022
Subjects:
Online Access:View Fulltext in Publisher
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020 |a 22964185 (ISSN) 
245 1 0 |a Preparation and Evaluation of Liposomes and Niosomes Containing Total Ginsenosides for Anti-Photoaging Therapy 
260 0 |b Frontiers Media S.A.  |c 2022 
856 |z View Fulltext in Publisher  |u https://doi.org/10.3389/fbioe.2022.874827 
520 3 |a Ginsenosides are the principal bioactive compounds of ginseng. Total ginsenosides (GS) contain a variety of saponin monomers, which have potent anti-photoaging activity and improve the skin barrier function. To enhance the efficiency of GS transdermal absorption, GS liposomes (GSLs) and GS niosomes (GSNs) were formulated as delivery vehicles. Based on the clarified and optimized formulation process, GSL and GSN were prepared. The structure, cumulative transmittance, skin retention, total transmittance, and bioactivity of GSLs and GSNs were characterized. GSL and GSN were shown to inhibit lipid peroxidation and increase the contents of superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) in human keratinocytes (HaCaTs). In addition, HaCAT cell migration, proliferation, and GS cellular uptake were significantly increased. The therapeutic effects of GSL and GSN were also evaluated in a rat model of photoaging. Histopathological changes were assessed in rat skin treated with GSL, GSN, or GS by hematoxylin–eosin (H&E) and aldehyde fuchsine staining. Malondialdehyde (MDA), SOD, GSH-Px, matrix metalloproteinases (MMPs), interleukin-6 (IL-6), interleukin-1β (IL-1β), and tumor necrosis factor-α (TNF-α) expression levels were determined. Results indicated that the optimal formulation of GSL used soybean lecithin (SPC) as the phospholipid, with a lipid–drug ratio of 1:0.4 and a phospholipid–cholesterol ratio of 1:3.5. The optimal temperature for the preparation process of GSN by ethanol injection was 65°C, with a ratio of the organic phase to aqueous phase of 1:9. It was demonstrated that the cumulative release rate, skin retention rate, and total transmission rate of GSL-7 at 24 h were higher than those of GSN-4 and GS. GSL-7 significantly inhibited skin lipid peroxidation caused by ultraviolet (UV) radiation. In addition, GSL-7 reduced the contents of MMPs and inflammatory cytokines in skin tissue. In conclusion, GSL-7 may reduce skin aging caused by UV radiation and contribute to skin tissue repair. Copyright © 2022 Jin, Liu, Lu, Yang, Chen, Zhou, Qiu and Jin. 
650 0 4 |a Aldehydes 
650 0 4 |a Cell death 
650 0 4 |a Controlled drug delivery 
650 0 4 |a Enzymes 
650 0 4 |a Ginsenosides 
650 0 4 |a liposomes 
650 0 4 |a Liposomes 
650 0 4 |a matrix 
650 0 4 |a Metalloproteinases 
650 0 4 |a niosomes 
650 0 4 |a Niosomes 
650 0 4 |a Oxidation 
650 0 4 |a Phospholipids 
650 0 4 |a photoaging 
650 0 4 |a Photo-aging 
650 0 4 |a Rats 
650 0 4 |a Skin retentions 
650 0 4 |a Super oxide dismutase 
650 0 4 |a Superoxide dismutases 
650 0 4 |a Targeted drug delivery 
650 0 4 |a Total ginsenoside 
650 0 4 |a total ginsenosides 
650 0 4 |a transdermal delivery 
650 0 4 |a Transdermal delivery 
700 1 |a Chen, J.  |e author 
700 1 |a Jin, Y.  |e author 
700 1 |a Jin, Y.  |e author 
700 1 |a Liu, D.  |e author 
700 1 |a Lu, Z.  |e author 
700 1 |a Qiu, Z.  |e author 
700 1 |a Yang, L.  |e author 
700 1 |a Zhou, X.  |e author 
773 |t Frontiers in Bioengineering and Biotechnology