Poly(HEMA) hydrogels with controlled pore architecture for tissue regeneration applications
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Biocompatible Materials chemistry MeSH
- Hydrogels chemistry MeSH
- Microscopy, Electron, Scanning MeSH
- Polyamines chemistry MeSH
- Polyhydroxyethyl Methacrylate analogs & derivatives chemistry MeSH
- Guided Tissue Regeneration * MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Biocompatible Materials MeSH
- Hydrogels MeSH
- poly(2-hydroxyethyl methacrylate)-polyamine graft copolymer MeSH Browser
- Polyamines MeSH
- Polyhydroxyethyl Methacrylate MeSH
The technique for fabrication of soft porous hydrogels, in which both the size and the orientation of inner pores can be controlled, was developed. Three-dimensional hydrophilic gels based on poly[2-hydroxyethyl methacrylate] are designed as scaffolds for regeneration of soft tissues, e.g., nerve tissue. Anisotropic macropores of the size ranging from 10 to 50 microm were formed (1) by using a porogen-leaching method with a solid organic porogen, (2) by phase-separation during gelation in solvent-nonsolvent mixture, or (3) by combination of solid porogen elimination and phase-separation. As a porogen, poly(L-lactide) fibers were applied and consequently washed away under mild conditions to obtain desired spatial orientation of pores. Highly water-swollen polymer gels were characterized with high pressure (low vacuum) scanning electron microscopy (AquaSEM). The morphology of voids remaining after removing the solid PLLA porogen (the macropores) was clearly shown.
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