期刊文献+

聚乳酸-壳聚糖接枝共聚物的制备及性能 被引量:5

The Synthesis and Properties of Poly(L-Lactide)-Chitosan Graft Copolymer
下载PDF
导出
摘要 以L-乳酸(LLA)和壳聚糖(CS)为原料,4-(二甲胺基)吡啶(DMAP)及N,N′-二环己基碳酰亚胺(DCC)为催化剂在室温下,通过直接缩合方法制备了聚乳酸-壳聚糖接枝共聚物(PLLA-CS)。采用IR、1H-NMR及薄板毛细渗透法对其结构进行了表征。探讨了原料配比、催化剂用量、LLA的二氯甲烷溶液浓度、反应时间等对共聚物收率和亲水性的影响。得到最佳工艺条件:-NH2∶LLA为1∶15,DCC∶LLA为1∶1,LLA的二氯甲烷溶液浓度为1.88 mol/L,反应时间为24 h。此方法合成路线短、反应条件温和。聚乳酸-壳聚糖接枝共聚物具有良好的细胞亲和性,有望成为一类优良的组织工程材料。 Graft copolymerization of L-lactide(LLA) onto chitosan(CS) was carried out by the direct polycondensation using 4-(dimethylamino) pyridine(DMAP) and N,N′-dicyclohexylcarboniimide(DCC) as catalyst in dichloromethane at room temperature to obtain poly(L-lactide)-chitosan(PLLA-CS) graft copolymers.The graft copolymers were characterized by IR,1H-NMR and thin-layer wicking technique.Grafting studies indicate that the ratio of raw materials(-NH2∶LLA),the amount of catalyst,the concentration of LLA and the reaction time influence the yield and contact angle of the copolymer.The optimum reaction conditions are as follows: the ratio of-NH2 to LLA 1∶15,the ratio of DCC to LLA 1∶1,the concentration of LLA 1.88 mol/L and reaction time 24 h.On the conditions,the yield of PLLA-CS copolymer is high and the contact angle is small.The grafting of LLA onto CS resulted in graft copolymers having increases the hydrophilicity.The results prove that the synthesis process has short route,simple technology,and mild conditions.
出处 《高分子材料科学与工程》 EI CAS CSCD 北大核心 2009年第10期139-141,145,共4页 Polymer Materials Science & Engineering
基金 陕西省13115科技创新工程重大科技专项项目计划(2007ZDKG-50)资助
关键词 聚(L-乳酸) 壳聚糖 接枝共聚 接触角 poly(L-lactide) chitosan grafting copolymer contact angle
  • 相关文献

参考文献7

  • 1李永刚,潘君,赵明媚,牛旭锋,王远亮.生物活性聚乳酸的研究[J].高分子材料科学与工程,2006,22(6):28-31. 被引量:9
  • 2LUCKACHAN G E, PILLAI C K S. Chitosan/oligo L-lactide graft copotymers: effect of hydrophobic side chains on the physico-chemical properties and biodegradability [ J ]. Carbohydrate Polymers, 2006, 64(2) : 254-266.
  • 3LIU Y, TIAN F, HU K A. Synthesis and characterization of a brush-like copolymer of polylactide grafted onto chitosan [J ]. Carbohydrate Research, 2004, 339(4): 845-851.
  • 4WU Y, ZHENG Y L, YANG W L, et al. Synthesis and characterization of a novel amphiphilic chitosan-polylactide graft copolymer[J]. Carbohydrate Polymers, 2005, 59(2): 165-171.
  • 5QU X, WIRSEN A, ALBERTSSON A C. Novel pH-sensitive chitosan hydrogels: swelling behavior and states of water [J ]. Polymer, 2000, 41(12) : 4589-4598.
  • 6YAO F L, CHEN W, WANG H, et al. A study on cytocompatible poly(chitosan-g-L-lactic acid) [ J ]. Polymer, 2003, 44 ( 21 ) : 6435- 6441.
  • 7储鸿,崔正刚.薄板毛细渗透法测定粉体接触角和表面能成分[J].江南大学学报(自然科学版),2005,4(3):302-305. 被引量:2

二级参考文献45

  • 1崔正刚,B.P.Binks,J.H.Clint.薄层毛细渗透技术测定多孔性固体颗粒的表面能成分[J].日用化学工业,2004,34(4):207-210. 被引量:8
  • 2Costanzo P M, Wu W, Giese R F, et al. Comparison between direct contact angle measurements and thin layer wicking on synthetic monosized cuboid hematite particles [J]. Langmuir, 1995, (11):1827-1830.
  • 3Li Z, Giese R F, van Oss C J, etal. The surface thermodynamic properties of talctreated with octadecylamine[J]. Colloid and Interface Sci, 1993, 156: 279-284.
  • 4Li Z, Giese R F, van Oss C J. Surface thermodynamic properties of synthetic hydrotalcite compounds[J]. Langmuir, 1994, 10: 330-333.
  • 5Chibowski E, Holysz L. Use of washburn equation for surface free energy determination[J]. Langmuir, 1992, 8:710-716.
  • 6Holysz L, Chibowski E. Surface free energy components of alumina from thin-layer wicking[J]. Langmuir, 1992, 8:717-721.
  • 7Chibowski E , Gonzalez-Caballero F. Theory and practice of thin-layer wicking[J]. Langmuir, 1993, 9:330-340.
  • 8Hoffman R L. A study of the advancing interface, I. interface shape in liquid-gas systems[J]. Colloid and Interface Sci, 1975, 50(2): 228-241.
  • 9Legait B, Sourieau P. Effect of geometry on advancing contact angle in fine capillaries[J]. Colloid and Interface Sci,1985, 107(1): 14-20.
  • 10Morrow N R, Nguyen M D. Effect of interface velocity on dynamic contact angle at rough surfaces[J]. Colloid and Interface Sci, 1982, 89(2):523-531.

共引文献9

同被引文献181

引证文献5

二级引证文献36

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部