Literature DB >> 15588891

A biomedical library of serinol-derived polyesters.

Jenny Rickerby1, Roopa Prabhakar, Anita Patel, Jonathan Knowles, Steve Brocchini.   

Abstract

Polyesters derived from glycerol and serinol were prepared. These polyesters were designed to be potential surrogate polymers for poly(glycolic acid) (PGA) to extend the properties that aliphatic biomedical polyesters could encompass. The 1- and 2-substituted glycerol derived monomers were liquids and difficult to polymerize reproducibly. In contrast the N-substituted serinol monomers were solids and easy to prepare. Each of the four N-substituted serinol-diol monomers was polymerized in a parallel fashion with each of the four commercially available diacids to produce a small library of 16 polyesters. Glass transition and contact angle values were determined to ascertain structure-property correlations due to defined chemical changes in the polymer mainchain and pendent chain. A serinol-derived precursor polymer was also prepared.

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Year:  2005        PMID: 15588891     DOI: 10.1016/j.jconrel.2004.07.021

Source DB:  PubMed          Journal:  J Control Release        ISSN: 0168-3659            Impact factor:   9.776


  2 in total

1.  Azlactone-functionalized polymers as reactive templates for parallel polymer synthesis: synthesis and screening of a small library of cationic polymers in the context of DNA delivery.

Authors:  Bin Sun; Xianghui Liu; Maren E Buck; David M Lynn
Journal:  Chem Commun (Camb)       Date:  2010-02-19       Impact factor: 6.222

2.  A functionalizable reverse thermal gel based on a polyurethane/PEG block copolymer.

Authors:  Daewon Park; Wei Wu; Yadong Wang
Journal:  Biomaterials       Date:  2011-01       Impact factor: 12.479

  2 in total

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