Synthesis of a novel amphiphilic polymer containing nucleobases in the self-organized nanospheres

被引:4
|
作者
Zhang, Xiao [1 ]
He, Zhenfeng [1 ]
Li, Guangquan [1 ]
Zhang, Yujian [1 ]
Li, Guowen [1 ]
机构
[1] Jilin Univ, State Key Lab Supramol Struct & Mat, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
Amphiphilic; FT-IR; Molecular recognition; Nanoparticles; Self-organization; MOLECULAR RECOGNITION; SUPRAMOLECULAR POLYMERS; ACID-DERIVATIVES; AQUEOUS MICELLES; WATER; ADENINE; CORE;
D O I
10.1007/s10965-009-9312-9
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A simple strategy to achieve molecular recognition in water is to make the polymers self-organized into nanospheres which could incorporate the functional groups containing hydrogen bonding sites into hydrophobic-lipophilic regions. A novel amphiphilic polymer, Poly(polyoxyethylene-600)-oxy-5-(6-(1-thymine)hexyl)) isophthaloyl (PPETHI), has been synthesized. The PPETHI polymer could self-organize into nanospheres in dilute aqueous solution, which were 150-300 nm in diameter as estimated by SEM. The isophthaloyl with side hexyl thymine of the polymer self-organized into hydrophobic regions and the PEG surrounded it. Molecular recognition between thymine in PPETHI polymer and adenine substrate has been studied by FT-IR. The FT-IR studies demonstrate that C-4=O of thymine has recognized with N-H of adenine through complementary nucleobases. It shows that the typical characteristic band at 3,352 cm(-1) of N-H stretching vibration of adenine shifted to 3,373 cm(-1) and the band at 1,685 cm(-1) of C-4=O of thymine shifted to 1,680 cm(-1). To confirm the formation of hydrogen bonds, the N-H band at 3,373 cm(-1) and C-4=O band at 1,680 cm(-1) have retrieved to 3,312 cm(-1) and 1,685 cm(-1) respectively upon heating to 115 A degrees C or higher by means of variable temperature FT-IR. The formations of hydrogen-bonds between thymine in the polymer and adenine substrate in nanospheres were confirmed. It could enhance their interaction and loading capacity.
引用
收藏
页码:255 / 263
页数:9
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