Crosslinkable citronellol containing polyphosphazenes and their biomedical potential

Jessica L. Nichol, Nicole L. Morozowich, Thomas E. Decker, Harry R. Allcock

Research output: Contribution to journalArticlepeer-review

10 Scopus citations

Abstract

An increased focus exists on the development of materials that might serve as ligament or tendon tissue engineering scaffolds. Requirements for a suitable candidate polymer include biodegradability, biocompatibility, and elasticity. In an attempt to meet these requirements novel citronellol-containing polyphosphazenes were synthesized, characterized, and crosslinked to generate elastomers. Citronellol was chosen as a side group due to its anti-inflammatory properties in addition to the presence of a double bond in its structure to permit polymer crosslinking. Alanine ethyl ester was chosen as a co-substituent to tune hydrolysis rates without severely affecting the glass transition temperatures of the final polymers. Hydrolysis of the uncrosslinked polymers in the form of films in deionized water at 37 C showed between ∼8 and 16% mass loss and between a ∼28 and 88% molecular weight decline over 12 weeks. Polymers were also crosslinked using ultraviolet radiation for increasing amounts of time. Preliminary mechanical testing of the homo-citronellol polymer indicated increasing modulus and decreasing tensile strength with increased crosslink density.

Original languageEnglish (US)
Pages (from-to)2258-2265
Number of pages8
JournalJournal of Polymer Science, Part A: Polymer Chemistry
Volume52
Issue number16
DOIs
StatePublished - Aug 15 2014

All Science Journal Classification (ASJC) codes

  • Polymers and Plastics
  • Organic Chemistry
  • Materials Chemistry

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