## Abstract Four different poly(ether urethane) gels were prepared by polyaddition of saccharide derivatives (1, 2, 3α, or 3β) and poly(propylene glycol) with an L‐lysine‐derived diisocyanate, methyl (__S__)‐2,6‐diisocyanatohexanoate (4). Dibutyltin dilaurate and triisocyanate 5, that was also deri
Swelling behavior and controlled release of new hydrolyzable poly(ether urethane) gels derived from saccharide and L-lysine derivatives and poly(ethylene glycol)
✍ Scribed by Sirinat Wibullucksanakul; Kazuhiko Hashimoto; Masahiko Okada
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 583 KB
- Volume
- 197
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
New hydrolyzable gels bearing saccharide, L‐lysine, and poly(oxyethylene) moieties were prepared via polyaddition of methyl ß‐D‐glucofuranosidurono‐6,3‐lactone (1) and poly(ethylene glycol) PEG, M~n~ = 1000 with an L‐lysine derivative, methyl (S)‐2,6‐diisocyanatohexanoate (2), using dibutyltin dilaurate and triisocyanate 3 as a catalyst and a crosslinking agent, respectively. The swelling ratio and rate of hydrolysis of these gels in phosphate buffers increased with the content of PEG. Hydrolysis of these gels was enhanced by increasing the pH of phosphate buffer solution in the range from 5.5 to 8.0, while the gel having only repeating units derived from 1 and 2 but no PEG was hardly hydrolyzed in any buffer solutions (pH 5.5, 7.0, 8.0). The release of hydrophilic 5(6)‐carboxyfluorescein (CF) from these gels in buffer solution of pH 8.0 was faster than that of hydrophobic magnesium 8‐anilino‐1‐naphthalenesulfonate (ANS). The release of ANS from the gel was enhanced with the swelling caused by hydrolysis.
📜 SIMILAR VOLUMES
Poly(ether urethanes) obtained by the copolymerization of poly(ethylene glycol) (PEG) and lysine ethyl ester (LysOEt) are elastomeric materials that can be processed readily to form flexible, soft films. In view of these desirable physicomechanical properties, the potential use of these new material