Macroporous poly(L-lactide) scaffold 1. Preparation of a macroporous scaffold by liquid-liquid phase separation of a PLLA-dioxane-water system

被引:107
作者
Hua, FJ [1 ]
Kim, GE [1 ]
Lee, JD [1 ]
Son, YK [1 ]
Lee, DS [1 ]
机构
[1] Sungkyunkwan Univ, Dept Polymer Sci & Engn, Ctr Adv Funct Polymers, Suwon 440746, Kyungki, South Korea
来源
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH | 2002年 / 63卷 / 02期
关键词
PLLA; macroporous scaffold; thermally induced phase separation; gelation;
D O I
10.1002/jbm.10121.abs
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A biodegradabIe poly(L-lactic acid) (PLLA) macroporous scaffold with a regular and highly interconnected structure in the size range from 50 to 150 mu m was fabricated from a PLLA-dioxane-water ternary system with the use of the thermally induced phase separation (TIPS) process. The phase diagram of PLLA with molecular weight above 200,000 was measured. It was found that a small change in the water content in the solvent caused a large shift in the cloud-point temperature. The porous morphology of the scaffold was closely related to the quenching route and formulation parameters, including polymer concentration, quenching temperature, aging time, and solvent composition of the ternary system. The porous morphology development in the scaffold was recorded as a function of aging time by scanning electronic microscopy (SEM). For systems with lower polymer concentrations (<4.5 wt%), polymer sedimentation occurred in the later stages of phase separation. A slight increase in the water content of the solvent mixture caused the sedimentation boundary to expand to higher polymer concentration. For systems with higher polymer concentrations (greater than or equal to4.5 wt%), the development of phase separation was restricted by gelation that resulted from the crystallization of the PLLA chains. This gelation effect was greater at high polymer concentrations and low quenching temperatures. The macroporous expected scaffold could be optimized from the slow development of phase separation during the long coarsening process. (C) 2002 John Wiley Sons, Inc.
引用
收藏
页码:161 / 167
页数:7
相关论文
共 37 条
[1]  
[Anonymous], 1992, ANGEW CHEM-GER EDIT, DOI DOI 10.1002/ANGE.19971091244
[2]  
ANTHONY A, 1997, SYNTHETIC BIODEGRADA
[3]  
Castro A. J., 1981, US Pat, Patent No. 4247498
[4]   The effects of diluent molecular weight on the structure of thermally-induced phase separation membrane [J].
Cha, BJ ;
Char, K ;
Kim, JJ ;
Kim, SS ;
Kim, CK .
JOURNAL OF MEMBRANE SCIENCE, 1995, 108 (03) :219-229
[5]  
FEED L, 1993, J BIOMED MATER RES, V27, P11
[6]   BIODEGRADABLE POLYMER SCAFFOLDS FOR TISSUE ENGINEERING [J].
FREED, LE ;
VUNJAKNOVAKOVIC, G ;
BIRON, RJ ;
EAGLES, DB ;
LESNOY, DC ;
BARLOW, SK ;
LANGER, R .
BIO-TECHNOLOGY, 1994, 12 (07) :689-693
[7]  
Harris LD, 1998, J BIOMED MATER RES, V42, P396, DOI 10.1002/(SICI)1097-4636(19981205)42:3<396::AID-JBM7>3.3.CO
[8]  
2-P
[9]   THERMOREVERSIBLE GELATION OF ATACTIC POLYSTYRENE - PHASE-TRANSFORMATION AND MORPHOLOGY [J].
HIKMET, RM ;
CALLISTER, S ;
KELLER, A .
POLYMER, 1988, 29 (08) :1378-1388
[10]  
HO H, 1995, TISSUE ENG, V1, P15