Creation of Chitosan-Based Nanocapsule-in-Nanofiber Structures for Hydrophobic/Hydrophilic Drug Co-Delivery and Their Dressing Applications in Diabetic Wounds.
Zheng-Ian LinTzu-Hsien TsaiKuan-Chi YuYu-Hsun NienRu-Ping LiuGuan-Lin LiuPei-Ling ChiYi-Ping FangBao-Tsan KoWing-Cheung LawCheng ZhouKen-Tye YongPei-Wen ChengChih-Kuang ChenPublished in: Macromolecular bioscience (2023)
Nanofiber meshes (NFMs) loading with therapeutic agents are very often employed to treat hard-to-heal wounds such as diabetic wounds. However, most of the NFMs have limited capability to load multiple or hydrophilicity distinctive-therapeutic agents. The therapy strategy is therefore significantly hampered. To tackle the innate drawback associated with the drug loading versatility, a chitosan-based nanocapsule-in-nanofiber (NC-in-NF) structural NFM system is developed for simultaneous loading of hydrophobic and hydrophilic drugs. Oleic acid-modified chitosan is first converted into NCs by our developed mini-emulsion interfacial cross-linking procedure, followed by loading a hydrophobic anti-inflammatory agent Curcumin (Cur) into the NCs. Sequentially, the Cur-loaded NCs are successfully introduced into reductant-responsive maleoyl functional chitosan/polyvinyl alcohol NFMs containing a hydrophilic antibiotic Tetracycline hydrochloride. Having a co-loading capability for hydrophilicity distinctive agents, biocompatibility and a controlled release property, the resulting NFMs have demonstrated the efficacy on promoting wound healing either in normal or diabetic rats. This article is protected by copyright. All rights reserved.
Keyphrases
- wound healing
- diabetic rats
- ionic liquid
- oxidative stress
- liquid chromatography
- drug delivery
- anti inflammatory
- immune response
- emergency department
- signaling pathway
- type diabetes
- stem cells
- cancer therapy
- high resolution
- mass spectrometry
- drug induced
- lps induced
- inflammatory response
- molecular dynamics simulations
- adverse drug