Poly (L-lactide)-poly (oxyethylene)-poly (L-lactide) block copolymers obtained in bulk, by a ring opening mechanism, from poly(ethylene glycol)s (PEG)s and L-lactide (LA), at 120-1 40 Β°C, in the absence of added catalysts are described. By using PEGs with different molecular masses, 3000 and 35 000,
Self-assembly of poly(ethylene glycol)-based block copolymers for biomedical applications
β Scribed by Hidenori Otsuka; Yukio Nagasaki; Kazunori Kataoka
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- English
- Weight
- 622 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1359-0294
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β¦ Synopsis
Nanostructure fabrication from block copolymers is discussed in this review paper. Particularly, novel approaches for the Ε½ . Ε½ . construction of functionalized poly ethylene glycol PEG layers on surfaces were focused to attain the specific adsorption of a target protein through PEG-conjugated ligands with a minimal non-specific adsorption of other proteins. Furthermore, surface organization of block copolymer micelles with cross-linking cores was described from the standpoint of preparation of a new functional surface-coating with a unique macromolecular architecture. The micelle-attached surface and the thin hydrogel layer made by layered micelles exhibited non-fouling properties and worked as a reservoir for hydrophobic reagents. These PEG-functionalized surface in brush form or in micelle form can be used in diverse fields of medicine and biology to construct high-performance medical devices including scaffolds for tissue engineering and matrices for drug delivery systems.
π SIMILAR VOLUMES
The polymerization of epsilon-caprolactone (epsilon-CL) was initiated by the terminal alcohol of methoxy poly(ethylene glycol) (MPEG) as an initiator via activated ring-opening polymerization in the presence of HCl. Et2O as a monomer activator. The molecular weights of the poly(epsilon-caprolactone)