Nanotechnology-driven wound healing potential of asiaticoside: a comprehensive review
Asiaticoside (AC) is a naturally occurring phytoconstituent that aids in wound healing by stimulating collagen biosynthesis. However, the physical properties of AC, such as its high molecular weight (959.12 g mol −1 ), poor water solubility, and low permeability, restrict its therapeutic benefits. A...
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Veröffentlicht in: | RSC pharmaceutics 2024-04, Vol.1 (1), p.9-36 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Asiaticoside (AC) is a naturally occurring phytoconstituent that aids in wound healing by stimulating collagen biosynthesis. However, the physical properties of AC, such as its high molecular weight (959.12 g mol
−1
), poor water solubility, and low permeability, restrict its therapeutic benefits. Additionally, the management of inflammation and angiogenesis in wound healing using AC-loaded wound dressings can be challenging in terms of its delivery across the skin layers. These challenges can be rectified by utilizing nanotechnology. The concept of nanotechnology is widely utilized in dermatology to boost the therapeutic efficacy of the entrapped drug. The AC-loaded nano-carriers deliver the drug at their target site in order to increase their efficacy, stability, and safety. These carriers efficiently distribute the loaded drug to the different skin layers. The current review focuses on the limitations associated with the topical administration of asiaticoside and the many initiatives made so far for effective and safe topical delivery using innovative constituents and techniques, along with other potential benefits of AC in wound healing, diabetes, inflammation, and depression.
The physical properties of asiaticoside (AC), such as its high molecular weight, poor water solubility, and low permeability, restrict its therapeutic benefits. AC-loaded nano-carriers overcome AC limitations in wound healing by enhancing delivery efficiency, stability, and safety. |
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ISSN: | 2976-8713 2976-8713 |
DOI: | 10.1039/d3pm00024a |