Molecular Recognition Induced Self-Assembly of Diblock Copolymers: Microspheres to Vesicles

被引:10
|
作者
Uzun, Oktay [1 ]
Sanyal, Amitav [2 ]
Jeong, Youngdo [1 ]
Rotello, Vincent M. [1 ]
机构
[1] Univ Massachusetts, Dept Chem, Amherst, MA 01003 USA
[2] Bogazici Univ, Dept Chem, TR-34342 Istanbul, Turkey
基金
美国国家科学基金会;
关键词
block copolymers; encapsulation; molecular recognition; polymersomes; self-assembled microspheres; GIANT POLYMER VESICLES; IN-VIVO; SUPRAMOLECULAR POLYMERS; LIPID-BILAYERS; SYSTEMS; SURFACE; MORPHOLOGY; GENE; SIZE; NANOPARTICLES;
D O I
10.1002/mabi.200900455
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Random diblock copolymer scaffolds grafted with diamidopyridine (DAP) hydrogen bonding recognition units self-assembled to furnish microspheres when mixed with monoblock copolymers decorated with complementary recognition elements. Through choice of block length, microspheres of various sizes could be produced. The relative length of the two blocks plays a crucial role in determining the formation of aggregates. PEG-b-P(S-co-S-DAP) diblock copolymer was used to fabricate recognition induced pegylated microspheres, by non-covalent cross-linking with monoblock copolymer functionalized with complementary thymine (Thy) units. These self-assembled microspheres can be efficiently crosslinked via photochemical [2 pi(s) + 2 pi(s)] cycloaddition with the resultant morphology change into vesicular structures.
引用
收藏
页码:481 / 487
页数:7
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