Pasty injectable biodegradable polymers derived from natural acids

Michal Y. Krasko, Abraham J. Domb

Research output: Contribution to journalArticlepeer-review

10 Scopus citations


Pasty biodegradable polymers that can be mixed with drugs at room temperature and injected to tissue as neat composition are advantageous as they allow simple preparation and delivery of drugs, particularly for heat sensitive drugs. A series of biodegradable pasty poly (ester-anhydride)s were prepared from alkanedicarboxylic acids and ricinoleic acid and its oligomers by transesterification-repolymerization method. The polymers were characterized by common spectroscopic, chromatography, and thermal methods. Polymers containing 70% ricinoleic acid and 30% linear dicarboxylic acids with 4-10 methylene groups were synthesized. The melting point of these poly (ester-anhydride)s increased as the number of methylenes in the alkanedicarboxylic acid increased. Use of short oligomers of ricinoleic acid instead of ricinoleic acid itself increased the melting point and decreased the softness of the resulting polymers. The polymers released model drugs for a few weeks while being degraded to their fatty acid counterparts. Copolymerization of alkanedicarboxylic acids with ricinoleic acid resulted in pasty biodegradable polymers useful as injectable carriers for drugs.

Original languageEnglish
Pages (from-to)1138-1145
Number of pages8
JournalJournal of Biomedical Materials Research - Part A
Issue number4
StatePublished - 15 Dec 2007
Externally publishedYes


  • Controlled release
  • Fatty acids
  • Gelling polymers
  • Poly(ester-anhydride)s
  • Ricinoleic acid


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