Innovative Solid Lipid Nanoparticle-Enriched Hydrogels for Enhanced Topical Delivery of L-Glutathione: A Novel Approach to Anti-Ageing
<b>Background:</b> Skin ageing, driven predominantly by oxidative stress from reactive oxygen species (ROS) induced by environmental factors like ultraviolet A (UVA) radiation, accounts for approximately 80% of extrinsic skin damage. L-glutathione (GSH), a potent antioxidant, holds promise in combating UVA-induced oxidative stress. However, its instability and limited penetration through the stratum corneum hinder its topical application. This study introduces a novel solid lipid nanoparticle (SLN)-enriched hydrogel designed to enhance GSH stability, skin penetration, and sustained release for anti-ageing applications. <b>Methods:</b> GSH-loaded SLNs were prepared via a double-emulsion technique and optimized using factorial design. These SLNs were incorporated into 1-3% (<i>w</i>/<i>v</i>) Carbopol hydrogels to produce a semi-solid formulation. The hydrogel's characteristics, including morphology, mechanical and rheological properties, drug release, stability, antioxidant activity, cytotoxicity, and skin penetration, were evaluated. <b>Results:</b> SEM and FTIR confirmed the uniform dispersion of SLNs within the hydrogel. The formulation exhibited desirable properties, including gel strength (5.1 ± 0.5 g), spreadability (33.6 ± 1.9 g·s), pseudoplasticity, and elasticity. In vitro studies revealed a biphasic GSH release profile, with sustained release over 72 h and over 70% cumulative release. The hydrogel significantly improved antioxidant capacity, protecting human fibroblasts from UVA-induced oxidative stress and enhancing cell viability. Stability studies indicated that 4 °C was optimal for storage over three months. Notably, the hydrogel enhanced GSH penetration through the stratum corneum by 3.7-fold. <b>Conclusions:</b> This SLN-enriched hydrogel effectively improves GSH topical delivery and antioxidant efficacy, providing a promising platform for anti-ageing and other bioactive compounds with similar delivery challenges.
Authors
- Manisha Sharma (ORCID: https://orcid.org/0000-0002-0692-3223)
- Mengyang Liu (ORCID: https://orcid.org/0000-0002-5927-5004)
- Guo‐Liang Lu (ORCID: https://orcid.org/0000-0002-2094-0820)
- Wenting Song (ORCID: https://orcid.org/0000-0003-0608-5298)
- Zhiwen Zhang (ORCID: https://orcid.org/0000-0002-0797-9448)
- Jingyuan Wen (ORCID: https://orcid.org/0000-0001-7833-5546)
Institutions
- University of Auckland (NZ)
- China Pharmaceutical University (CN)
- Fudan University (CN)
- Cancer Society of New Zealand (NZ)
- Maurice Wilkins Centre (NZ)
Publication Details
- Journal
- Pharmaceutics
- Published
- 2024-12-24
- DOI
- https://doi.org/10.3390/pharmaceutics17010004
- Citations
- 13
- Primary Topic
- Advanced Drug Delivery Systems
- Type
- article
- Field-Weighted Citation Impact
- 2.70