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Water-soluble polyamides as potential drug carriers. VIII. Poly(alkylene oxide)-grafted polyaspartamides bearing ethylenediamine side-group functions

โœ 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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โœฆ 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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โœ Gregg Caldwell; Eberhard W. Neuse; Axel G. Perlwitz ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 196 KB ๐Ÿ‘ 1 views

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