Solvent-induced morphological diversification in poly(L-lactide-b-ε-caprolactone) block copolymer thin films

被引:5
作者
Kikkawa, Yoshihiro [1 ]
Kurokawa, Kenji [2 ]
Kimura, Ryota [1 ]
Takahashi, Mayuko [1 ]
Kanesato, Masatoshi [1 ]
Abe, Hideki [2 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Photon Res Inst, Tsukuba, Ibaraki 3058562, Japan
[2] RIKEN Adv Sci Inst, Chem Anal Team, Wako, Saitama 3510198, Japan
关键词
Block copolymer; Atomic force microscopy; Thin film; Enzymatic degradation; Solvent; ATOMIC-FORCE MICROSCOPY; SOLID-STATE STRUCTURE; ENZYMATIC DEGRADATION; SINGLE-CRYSTALS; POLY(EPSILON-CAPROLACTONE); POLY(L-LACTIDE); CRYSTALLIZATION; GRAPHITE; ARRAYS; AFM;
D O I
10.1016/j.polymdegradstab.2010.01.005
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Biodegradable block copolymer of poly(L-lactide-b-epsilon-caprolactone) (P(LA-b-CL)) was dissolved in various solvents with different solubility as well as volatility, and spin-cast on a highly oriented pyrolytic graphite (HOPG) to prepare thin films. The surface morphologies were observed by using atomic force microscopy (AFM) in a dynamic force (tapping) mode. Particle like morphology was found in the thin films prepared form the dichloromethane and acetone. Higher volatility of dichloromethane and acetone resulted in the reflection of the particle like objects in the solution to HOPG substrate. In contrast, the P(LA-b-CL)s in toluene and 1,4-dioxane exhibited different morphologies compared to those in dichloromethane and acetone. Lower volatility of toluene and 1,4-dioxane assisted the epitaxial crystallization of PCL component along the HOPG lattice, that was revealed by enzymatic degradation of PLLA component by proteinase K. Thus, adjusting the solubility and solvent volatility for the film formation provided morphological divergence of the P(LA-b-CL) block copolymer, and this technique would be applicable for the surface patterning of biodegradable polymers. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1414 / 1420
页数:7
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