4.7 Article

Surface Eroding, Liquid Injectable Polymers Based on 5-Ethylene Ketal ε-Caprolactone

Journal

BIOMACROMOLECULES
Volume 12, Issue 10, Pages 3423-3431

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/bm200980a

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Funding

  1. Canadian Institutes of Health Research

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Liquid, injectable hydrophobic polymers are potentially useful as depot systems for localized drug delivery. Low molecular weight polymers of 5-ethylene ketal caprolactone and copolymers of this monomer with D,L-lactide were prepared, and their properties assessed with respect to their suitability for this purpose. The polymers were amorphous and of low viscosity, and the viscosity was adjustable by choice of initiator and/or by copolymerizing with D,L-lactide. Lower viscosity polymers were attained-by using 350 Da methoxy poly(ethylene glycol) as an initiator in comparison to to ocan-1-ol, while copolymerization with D,L-lactide increased viscosity. The initiator used had no significant effect on the rate of mass loss in vitro, and copolymers with D,L-lactide (DLLA) degraded faster than 5-ethylene ketal epsilon-caprolactone (EKC) homopolymers. For the EKC-based polymers, a nearly constant degradation rate was observed. This finding was attributed to the hydrolytic susceptibility of the EKC EKC ester linkage, which was comparable to that of DLLA DLLA, coupled with a higher molecular weight of the water-soluble degradation and the low initial molecular weight of the EKC-based polymers, Cytotoxicity of the hydrolyzed EKC monomer to 3T3 fibroblast cells was comparable to that of e-caprolactone, suggesting that polymers prepared from EKC may be well tolerated upon in vivo implantation.

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