School of Science, RMIT University, Melbourne, Victoria 3000, Australia.
CSIRO Manufacturing, Clayton, Victoria 3168, Australia.
J Biomed Mater Res B Appl Biomater. 2018 Jul;106(5):1712-1720. doi: 10.1002/jbm.b.33970. Epub 2017 Aug 31.
Mixed macrodiol based siloxane poly(urethane-urea)s (SiPUU) having number average molecular weights in the range 87-129 kDa/mol were synthesized to give elastomers with high tensile and tear strengths required to fabricate artificial heart valves. Polar functional groups were introduced into the soft segment to improve the poor segmental compatibility of siloxane polyurethanes. This was achieved by linking α,ω-bis(6-hydroxyethoxypropyl) poly(dimethylsiloxane) (PDMS) or poly(hexamethylene oxide) (PHMO) macrodiols with either 4,4'-methylenediphenyl diisocyanate (MDI), hexamethylene diisocyanate (HDI) or isophorone diisocyanate (IPDI) prior to polyurethane synthesis. The hard segment was composed of MDI, and a 1:1 mixture of 1,3-bis(4-hydroxybutyl)-1,1,3,3-tetramethyldisiloxane and 1,2-ethylene diamine. We report the effect of urethane linkers in soft segments on properties of the SiPUU. PHMO linked with either MDI or IPDI produced SiPUU with the highest tensile and tear strengths. Linking PDMS hardly affected the tensile strength; however, the tear strength was improved. The stress-strain curves showed no plastic deformation region typically observed for conventional polyurethanes indicating good creep resistance. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 106B: 1712-1720, 2018.
合成了数均分子量在 87-129 kDa/mol 范围内的混合大二醇基硅氧烷聚(氨酯-脲)(SiPUU),以赋予具有制造人工心脏瓣膜所需的高拉伸和撕裂强度的弹性体。将极性官能团引入软段中,以改善硅氧烷聚氨酯的较差的相区相容性。这是通过将 α,ω-双(6-羟乙氧基丙基)聚(二甲基硅氧烷)(PDMS)或聚(六亚甲基氧化物)(PHMO)大二醇与 4,4'-亚甲基二苯基二异氰酸酯(MDI),己二异氰酸酯(HDI)或异佛尔酮二异氰酸酯(IPDI)连接,然后进行聚氨酯合成来实现的。硬段由 MDI 和 1:1 混合物的 1,3-双(4-羟丁基)-1,1,3,3-四甲基二硅氧烷和 1,2-乙二胺组成。我们报告了软段中氨酯键合对 SiPUU 性能的影响。与 MDI 或 IPDI 连接的 PHMO 产生的 SiPUU 具有最高的拉伸和撕裂强度。连接 PDMS 几乎不会影响拉伸强度;但是,撕裂强度得到了改善。应力-应变曲线没有观察到常规聚氨酯通常存在的塑性变形区,表明具有良好的抗蠕变性。©2017 Wiley Periodicals,Inc. J Biomed Mater Res Part B:Appl Biomater,106B:1712-1720,2018。