The synthesis of side-chain-functionalized polyaspartamides as potential carrier polymers for medicinal agents is described. The nucleophilic ring opening in poly-D,L-succinimide, mediated by O, O-bis(2-aminopropyl)poly(ethylene oxide) (nominal molecular mass is 600) and ethanolamine under carefully
Water-soluble polyamides as potential drug carriers. VIII. Poly(alkylene oxide)-grafted polyaspartamides bearing ethylenediamine side-group functions
โ Scribed by Eberhard W. Neuse; Axel G. Perlwitz; Anna P. Barbosa
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 541 KB
- Volume
- 54
- Category
- Article
- ISSN
- 0021-8995
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โฆ Synopsis
In continuation of previous investigations of aspartamide-type polymers as drug carriers, polyaspartamides featuring hydrosolubilizing poly ( alkylene oxide ) side chains in addition to ethylenediamine side-group functions as potential drug-binding sites are synthesized from poly-D,L-succinimide by successive aminolytic ring-opening steps. Yields are in the range of 45-55%. Depending on selected feed ratios, the target polymers contain both the poly ( alkylene oxide ) and the ethylenediamine groups in systematically varied proportions. Compositions are determined microanalytically and from relative band intensities of the 'H-NMR spectra. The polymers dissolve smoothly and completely in aqueous media and thus fulfill the major design requirement of water solubility.
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