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作 者:伍国琳[1] 王铮[1] 林海[1] 张洁[1] 孙平川[1] 张国林[1] 王亦农[1] 马建标[1]
机构地区:[1]南开大学高分子化学研究所功能高分子材料重点实验室,天津300071
出 处:《高分子学报》2009年第12期1232-1237,共6页Acta Polymerica Sinica
基 金:天津市自然科学基金(基金号09JCYBJC03400)资助项目;国家重点基础研究发展计划(973计划前期研究专项;项目号2009CB626612)资助
摘 要:利用核磁共振方法研究了AB型双嵌段共聚物(MPEG45-b-PA32)在选择性溶剂中的自组装行为及胶束化过程.嵌段共聚物在三氟乙酸中聚氨基酸和聚乙二醇链段均处于自由运动状态,聚丙氨酸链段为无规线团结构.在向该溶液中逐渐加入氘代水的过程中,聚丙氨酸链段又重新聚集形成规整的二级结构.结合1H-NMR和COSY谱分析,结果显示这一自组装过程伴随着聚(L-丙氨酸)链段由无规线团向α-螺旋结构的构象转变,同时嵌段共聚物逐渐形成核-壳型胶束结构.利用透射电镜观察了所形成胶束的形态,嵌段共聚物主要形成粒径150 nm到220 nm的球形胶束.Poly ( ethylene glycol) methyl ether- block-poly (L-alanine) ( MPEG- b-PA) was synthesized with the initiation of MPEG-NH2. While MPEG is the hydrophilic block and PA is the hydrophobic block. It is known that poly(L-amino acid)s like polypeptides have their special secondary structures such as a-helix and β-sheet. 1H-NMR and COSY-NMR were used to monitor the micellization process of a poly(ethylene glycol) methyl ether-block-poly (L-alanine) copolymer ( MPEG45 - b-PA32 ) MPEG45- b-PA32 was dissolved in CF3 COOD first, while poly(L-alanine) blocks were in random coil structure. When D20 was added in this CF3COOD solution, MPEG45-b-PA32 could self- assemble into micelles. In the micellization process, mobility of PA blocks decreased while MPEG blocks kept very high mobility. Based on the chemical shifts and COSY data analysis, it was concluded that poly(amino acid) tended trend to form a-helix structure from random coil while the copolymer assembled in water. At the same time, transmission electron microscopy (TEM) results revealed that the diblock copolymer formed spherical micelles with the size of 150 - 220 nm in an aqueous medium.
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