Abstract
Four different classes of polyphosphazenes that can be designated as 'bioerodible' have been synthesized. In each polymer system, at least one of the side groups is hydrolytically labile. The degradation products of these reactions are phosphates, ammonia, glucose, and methylamine. The potential applications of α-D-glucosyl polyphosphazenes are of considerable interest. Drug molecules or peptides could be directly linked to the water-soluble polymer or to a crosslinked hydrogel. In vivo hydrolysis would release the glucose-bound pharmaceutical. Also, by use of a water-insolublizing cosubstituent, the potential exists to design a monlithic drug delivery system.
Original language | English (US) |
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Pages (from-to) | 180-181 |
Number of pages | 2 |
Journal | American Chemical Society, Polymer Preprints, Division of Polymer Chemistry |
Volume | 31 |
Issue number | 2 |
State | Published - Aug 1 1990 |
Event | Papers presented at the Washington, DC Meeting 1990 of the ACS, Division of Polymer Chemistry - Washington, DC, USA Duration: Aug 26 1990 → Aug 31 1990 |
All Science Journal Classification (ASJC) codes
- Materials Science(all)
- Polymers and Plastics
- Engineering(all)