Abstract
An amphiphilic porphyrin-cored, star-shaped poly (ε-caprolactone)-b-poly (ethylene glycol) (SPPCL-b-PEG) copolymer was synthesized and used as a building block for constructing supramolecular hydrogels. With the aid of α-cyclodextrin (α-CD), thixotropic and reversible supramolecular hydrogel could be formed by copolymers based on the host-guest inclusion complexation (IC). Due to the biodegradable and biocompatible properties, this IC-based supramolecular hydrogel was used as carrier for doxorubicin (DOX) delivery systems. The release results presented a triphasic drug-release profile and the release of this system lasted more than 3 weeks. Also, upon irradiation with light (650 nm), cytotoxic singlet oxygen (1O2) could be generated by porphyrin core and easily released from hydrogel matrix. Considering that both sustained-release drug delivery of hydrogels and porphyrin for photodynamic therapy (PDT) were achieved in a combined compound, this shear-thinning supramolecular hydrogel with porphyrin was elaborately designed as a promising replacement therapy to medium or advanced cancer for surgery.
| Original language | English |
|---|---|
| Pages (from-to) | 149-159 |
| Number of pages | 11 |
| Journal | European Polymer Journal |
| Volume | 66 |
| DOIs | |
| State | Published - May 2015 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
-
SDG 3 Good Health and Well-being
Keywords
- Block copolymer
- Drug delivery
- Photodynamic therapy
- Shear-thinning
- Supramolecular hydrogels
Fingerprint
Dive into the research topics of 'Rational design of shear-thinning supramolecular hydrogels with porphyrin for controlled chemotherapeutics release and photodynamic therapy'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver