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PBT/PEG/LA可降解纤维的结构与性能 被引量:2

Structure and Properties of PBT/PEG/LA Biodegradable Fiber
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摘要 在软硬段质量恒为5∶5,PEG分子量1000的PBT/PEG体系中添加一定摩尔含量的乳酸,合成了一系列PBT/PEG/LA嵌段共聚醚酯,其中乳酸占PBT硬段摩尔分数的0-30%。采用FT-IR,1^H-NMR,DSC等方法表征了材料的结构,并测试了力学性能及降解性能。主链硬段和热学性质分析表明,随着乳酸占原PBT/PEG共聚物中PBT摩尔分数的百分比由0增加至30%时,PBT摩尔分数从83.70%下降至58.58%,硬段熔点(Tm,h)也从196.3℃下降至170.1℃。力学性能测试表明,较高的LA摩尔含量有利于纤维降解,但使其断裂强度有所下降。PBT/PEG/LA纤维的可降解性能主要取决于其主链结构、聚集态以及LA的摩尔含量,降解后纤维的断裂强度保留率Y(%)与降解时间t(week)的关系满足回归方程:Y=A+B1×t+B2×t^2+B3×t^3+B4×t^4,相关系数R^2〉0.997。 A series of PBT/PEG/LA block copoly(ether-ester) with the constant mass ratio (r = 1 ) of soft to hard segment of PBT/PEG (Mn= 1000) and LA molar fraction to PET hard segment varying from 0 -30% were synthesized and characterized by means of intrinsic viscosity [ η], FF - IR, 1^H - NMR, DSC, mechanical properties and degradation behavior. The analysis on the hard segments in the copolymer chain and the thermodynamic properties showed that the molar faction of PBT decreased from 83.70% to 58.58% and the melting points (Tm.h) of hard segments decreased from 193.6 ℃ to 170.1 ℃ ,with the increase of LA molar ratio from 0 to 30% to the molar faction of PBT in the initial PBT/PEG copolymer. The mechanical properties testing showed that the higher molar fraction of LA impacts degradation of fibers, while the lower one improves the tensile strength. The biodegradable properties of PBT/PEG/LA fibers are related to its chain structure, collective structure and the molar faction of LA. The regression equation based on the correlations between the remaining percent of tensile strength Y( % ) of degradable fi bers and time of degradation t(week) is Y =A + B1 × t + B2 × t^2 + B3 × t^3 + B4 × t^4, and the coefficient of determi nation R^2 〉 0.997.
出处 《四川大学学报(工程科学版)》 EI CAS CSCD 北大核心 2007年第5期92-96,共5页 Journal of Sichuan University (Engineering Science Edition)
基金 成都市科学计划资助项目(200538121)
关键词 PBT/PEG 乳酸 降解 纤维 力学性能 PBT/PEG LA biodegradable fiber mechanical properties
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  • 1Roessler M,Wilke A,Griss P,et al.Missing osteoconductive effect of resorbable PEO/PBT copolymer in human bone defeets[J].Journal of Biomedical Materials Research,2000,53(2):167-173.
  • 2Deschamps A A,Claase M B,Sleijster W J,et al.Design of segmented poly(ether-ester)materials and structures for the tissue engineering of bone[J].Journal of Controlled Release,2002,78:175-186.
  • 3Bezemer J M,Radersma R,Grijpma D W,et al.Zero-order release of lysozyme from poly(ethylene-glycol)/poly(butylenete-rephthalate)matrices[J].Journal of Controlled Release,2000,64:179-192.
  • 4顺冠芸,潘华珍,吴翚.生物化学与分子生物学实验常用数据手册[M].北京:科学出版社,1999:13-20.
  • 5Betolho G,Queiros A,Gijsman P.Thermooxidative studies of poly (ether-esters)1.copolymer of poly (butylenes terephthalate) and poly(ethylene oxide)[J].Polymer Degradation and Stability,2000,67:13-20.
  • 6Audrey A D,Menno B C,WarnerieJ,et al.Design of segmented poly(ether ester)materials and structures for the tissue engineering of bone[J].Journal of Controlled Release,2002,78:175-186.
  • 7张勇,叶玲,冯增国,张爱英,田小娟,徐瑞兴.相同软硬段质量配比聚醚酯弹性体PEG/PBT的结构与表征[J].高等学校化学学报,2002,23(10):1982-1987. 被引量:15
  • 8张勇,冯庆玲,崔福斋,冯增国.不同软段长度PBT-co-PCT-b-PEG嵌段共聚物的结构与性能[J].高分子材料科学与工程,2005,21(1):180-183. 被引量:4
  • 9张爱英,冯增国,张勇,巴建华.聚乙二醇-b-聚对苯二甲酸丁二醇酯嵌段共聚物降解行为的研究[J].高等学校化学学报,2003,24(6):1122-1125. 被引量:8

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  • 1Iijima S. Helical microtubules of graphitic carbon[J]. Nature. 1991,354(6348): 56-58.
  • 2Ehbosen 丁,Ajayan P. I.arge-scale synthesis of carbon nanotubes[J]. Nature,1992,358(6383) : 220-222.
  • 3Dhar S. Liu Zhuang. Thomale Juergen, et al. Targeted single-wall carbon nanotube-mcdiated Pt (IV) prodrug deliveryusing folate as a homing cievicc[J]. Journal of the American Chemical Society.2008?130(vS4) : 1 1467-1 1476.
  • 4McDevitt M R.Chattopadhyay Dehjit, Jaggi Jaspreet S. et al. PET imaging of soluble ytlrium-86-labeled carbon nano-tubes in micc[J]. Public Library of Science one, 2007,2(9): e907-e917.
  • 5Hu Yongun,Smith David E, Ma Ke. et al. Targeted disruption of peptide transporter pcptl gene in mice significantlyreduces dipeptide absorption in intestine[J]. Molecular Pharmaceutics^ 2008,5(6):1122-1130.
  • 6Yang R, Yang X, Zhang Z. et al. Single-walled carbon nanotubes-mediated in vivo and in vitro delivery of siRNA intoantigen-pre.senting celLs[J]. Gene Therapy, 2006,13(24):1714-1723.
  • 7Pantarotto I), Briand J W Prato M,et al. Translocation of bioactive peptides across cell membranes by carbon n?mo-tuWs[J]. Chemical Communications, 2004( 1) : 16-17.
  • 8Liu Zhuang. Sun Xiaoming, Nakayama-Ratchford. et al. Supramolecular chemistry on water-soluble carbon nanotubcsfor drug loading and delivery[J]. American Chemical Society Nano. 2007, 1 (1) j50-56.
  • 9Shen Mingwu, Wang Suhe, Shi Xiangyang, et al. Polyethyleneimine-mcdiated functionalization of multi-walled carbonnanotubes: Synthesis, characterization, and in vitro toxicity assayQ]. The Journal of Chemical Physics: C,2009,113(8),3150-3156.
  • 10Zhang Xiaoke,Meng Lingjie, Lu Qinghua,et ai. Targeted delivery and controlled release of doxorubicin to cancer cellsusing modified single wall carbon nanotubes[J]. Biomaterials? 2009 , 30(30):6041-6047.

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