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Abstrakty
New segmented photocurable poly(ester-urethane)s were synthesized in bulk. First, the soft segment composed of the unsaturatcd dicarboxylic fumaric acid and a renewable dimer fatty acid diol was synthesized, thus giving the ester block. The hard urethane segments were built up of aliphatic diisocyanate and different chain extenders, namely 1,4-butanediol (BD) or glycerol (GLY). The photoinitiator was introduced by solution mixing and subsequent solvent casting and light-curable films were obtained. The structure of the materials was analyzed. The FT-IR and DSC studies were performed to verify the material chcmical and phase structure.
Czasopismo
Rocznik
Tom
Strony
175--180
Opis fizyczny
Bibliogr. 11 poz., rys., tab.
Twórcy
autor
autor
- Szczecin University of Technology, Polymer Institute, Division of Biomaterials and Microbiological Technologies, Pułaskiego 10, 70-322 Szczecin, Poland, jskrobot@zut.edu.pl
Bibliografia
- [1] Jeong B., Gutowska A., Trends Biotechnol, 2002,20,305.
- [2] Kumar A., Srivastava A., Yu GalacvL, Mattiasson B., Prog. Polym. Sei., 2007,32,1205.
- [3] Peter S.J., Miller M.J., Yashko A.W., Yaszemski M.J., Mikos A.G., J. Biomed Mater. Res., 1998,43(4), 422.
- [4] Tcmenoff J.S., Mikos A.G., Biomaterials, 2000,21,2405.
- [5] Burkoth A.K., Anseth K..S., Biomaterials, 2000,21,2395.
- [6] Bonzani I.C., Adhikari R., Houshyar S., Mayadunne S., Gunatillake P., Stevens M.M., Biomaterials, 2007,28,423.
- [7] Lelah M.D., Cooper J.L., Polyurethanes in medicine, 1987, CRC Press.
- [8] Prowans P., El Fray M., Slonccki J., Biomateriale, 2002,23,2973.
- [9] El Fray M., Nanostructured Elastomeric Biomaterials for Soft Tissue Reconstruction, Publishing House of the Warsaw University of Technology, Warszawa, 2003.
- [10] He S., TimmerM.D., Yaszemski M.J., Yasko A.W., Engel P.S., Mikos A.G., Polymer, 2001,42,1251.
- [11] Bryant S.J., Nuttclman C.R., Anseth K.S.,J. Biomater. Sei., Polym. Ed., 2000,11,439.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BPC2-0006-0026