Aggregation behavior of MPEG-PCL diblock copolymers in aqueous solutions and morphologies of the aggregates

被引:24
作者
Lu, Chengfei
Guo, Shengrong [1 ]
Liu, Li
Zhang, Yaqiong
Li, Zonghai
Gu, Jianren
机构
[1] Shanghai Jiao Tong Univ, Sch Pharm, Shanghai 200240, Peoples R China
[2] Chongqing Univ Med Sci, Pharmaceut Sch, Chongqing 400016, Peoples R China
[3] Shanghai Jiao Tong Univ, Natl Lab Oncogenes & Related Genes, Shanghai Canc Inst, Shanghai 200240, Peoples R China
关键词
AFM; aggregation; diblock copolymer; morphology;
D O I
10.1002/polb.20979
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理]; 080501 [材料物理与化学]; 081704 [应用化学];
摘要
Poly(ethylene glycol)-b-polycaprolactone (MPEG-PCL) diblock copolymers were synthesized via a ring-opening polymerization of epsilon-CL monomers with MPEG as an initiator. Their solubilities and apparent critical micelle concentrations (CMC) in aqueous solution were investigated as well as the determination of the micellar hydrodynamic diameter using dynamic light scattering (DLS). As PCL block length increased, the solubility and CMC decreased while diameters of micelles increased. The gel-sol transition behaviors were investigated using a vial tilting method. Aqueous solutions of copolymers undergo a gel to sol transition with increase in temperature when their polymer concentrations are above a critical gel concentration (CGC). The CGC of the copolymers and gel-sol transition temperature are influenced by the PCL chain length. The tapping mode AFM was performed by imaging the freeze-dried deposits from the copolymer solutions on mica to investigate a process from free chains to micelles and to gel. (c) 2006 Wiley Periodicals, Inc.
引用
收藏
页码:3406 / 3417
页数:12
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