Literature DB >> 12361610

Biocompatibility and degradation of poly(ether-ester) microspheres: in vitro and in vivo evaluation.

R van Dijkhuizen-Radersma1, S C Hesseling, P E Kaim, K de Groot, J M Bezemer.   

Abstract

Microspheres of a hydrophobic and a hydrophilic poly(ether-ester) copolymer were evaluated for their in vitro and in vivo biocompatibility and degradation. The microspheres prior to and after sterilization were tested for in vitro cytotoxicity. The in vivo biocompatibility of the poly(ethylene glycol) terephthalate and poly(butylene terephthalate) (PEGT/PBT) microspheres was evaluated subcutaneously and intramuscularly for 24 weeks in rabbits. The in vivo degradation of the microspheres was studied microscopically and compared to the in vitro degradation. The in vitro and in vivo studies showed the biocompatibility of the microspheres of both the hydrophobic and the hydrophilic PEGT/PBT copolymer. Extracts of these microspheres showed no cytotoxic reactivity in the in vitro cytotoxicity test. Sterilization of the microspheres by gamma irradiation did not affect the cytotoxicity. PEGT/PBT microspheres injected subcutaneously and intramuscularly in rabbits showed a mild tissue response in vivo, in terms of the inflammatory response, the foreign body reaction and the granulation tissue response. Although an in vitro degradation experiment showed a decrease in molecular weight due to hydrolysis, the in vivo degradation of the microspheres was slower than previously published. Copyright 2002 Elsevier Science Ltd.

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Year:  2002        PMID: 12361610     DOI: 10.1016/s0142-9612(02)00220-x

Source DB:  PubMed          Journal:  Biomaterials        ISSN: 0142-9612            Impact factor:   12.479


  11 in total

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2.  In vitro/in vivo correlation for 14C-methylated lysozyme release from poly(ether-ester) microspheres.

Authors:  R van Dijkhuizen-Radersma; S J Wright; L M Taylor; B A John; K de Groot; J M Bezemer
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3.  Development of biodegradable and injectable macromers based on poly(ethylene glycol) and diacid monomers.

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8.  Localized delivery of dexamethasone from electrospun fibers reduces the foreign body response.

Authors:  Nathaniel M Vacanti; Hao Cheng; Paulina S Hill; João D T Guerreiro; Tram T Dang; Minglin Ma; Shanée Watson; Nathaniel S Hwang; Robert Langer; Daniel G Anderson
Journal:  Biomacromolecules       Date:  2012-09-11       Impact factor: 6.988

9.  Intracellular degradation of microspheres based on cross-linked dextran hydrogels or amphiphilic block copolymers: a comparative raman microscopy study.

Authors:  Henk-Jan van Manen; Aart A van Apeldoorn; Ruud Verrijk; Clemens A van Blitterswijk; Cees Otto
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10.  Degradable lipid nanoparticles with predictable in vivo siRNA delivery activity.

Authors:  Kathryn A Whitehead; J Robert Dorkin; Arturo J Vegas; Philip H Chang; Omid Veiseh; Jonathan Matthews; Owen S Fenton; Yunlong Zhang; Karsten T Olejnik; Volkan Yesilyurt; Delai Chen; Scott Barros; Boris Klebanov; Tatiana Novobrantseva; Robert Langer; Daniel G Anderson
Journal:  Nat Commun       Date:  2014-06-27       Impact factor: 14.919

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