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Distinctive Nanogels as High-Efficiency Transdermal Carriers for Skin Wound Healing
- Source :
- Journal of biomedical nanotechnology. 16(3)
- Publication Year :
- 2020
-
Abstract
- We propose that nanogels (HLGs) prepared by simply blending an epidermal growth factor (EGF)-loaded hyaluronan (HA)-based nanoformulation and poloxamers can be efficient transdermal drug carriers. In particular, due to the thermogelling behavior of poloxamer, when the HLGs, which are liquid at room temperature, are applied to the skin's surface, they form a gel at skin temperature. First, lipid-based nanoformulations (EGF-LNs) were fabricated by the lipid thin film method and then chemically conjugated with HA on the surface of the films to prepare EGF-loaded HA-based nanoformulations (EGF-HLNs). Both EGF-LNs and EGF-HLNs exhibited a uniform size and spherical lamellar structure. The EGF-HLN was added to a poloxamer solution to form EGF-HLG, which is a liquid at room temperature and a gel at skin temperature. HLGs have been shown to be able to deliver and permeate EGF well into the skin using both in vitro and in vivo systems, thus serving as an effective transdermal delivery system. In addition, it has been confirmed that this system could be a possible implantable drug carrier. Therefore, HLGs, which are uncomplicated and easily prepared, are expected to be easily used not only in the pharmaceutical field but also in the cosmetic field.
- Subjects :
- Drug Carriers
Wound Healing
Materials science
integumentary system
Epidermal Growth Factor
Biomedical Engineering
Pharmaceutical Science
Medicine (miscellaneous)
Nanogels
Bioengineering
Permeation
Conjugated system
Poloxamer
Administration, Cutaneous
In vivo
General Materials Science
Lamellar structure
Drug carrier
Wound healing
hormones, hormone substitutes, and hormone antagonists
Biomedical engineering
Transdermal
Skin
Subjects
Details
- ISSN :
- 15507033
- Volume :
- 16
- Issue :
- 3
- Database :
- OpenAIRE
- Journal :
- Journal of biomedical nanotechnology
- Accession number :
- edsair.doi.dedup.....9b5f3b84130677b59445de9883cb01c0