Preparation and characterization of electrospun poly(L-lactic acid-co-succinic acid-co-1,4-butane diol) fibrous membranes

被引:17
作者
Jin, HJ
Hwang, MO
Yoon, JS
Lee, KH
Chin, IJ
Kim, MN
机构
[1] Inha Univ, Dept Polymer Sci & Engn, Inchon 402751, South Korea
[2] Sangmyung Univ, Dept Biol, Seoul 110743, South Korea
关键词
biodegradable copolymers; electrospinning; nanofibers; non-woven membranes; scaffolds; fibroblast cells;
D O I
10.1007/BF03219018
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly(L-lactic acid-co-succinic acid-co-1,4-butane diol) (PLASB) was synthesized by direct condensation copolymerization of L-lactic acid (LA), succinic acid (SA), and 1,4-butanediol (BD) in the bulk using titanium(IV) butoxide as a catalyst. The weight-average molecular weight of PLASB was 2.1 X 10(5) when the contents of SA and BD were each 0.5 mol/100 mol of LA. Electrospinning was used to fabricate porous membranes from this newly synthesized bioabsorbable PLASB dissolved in mixed solvents of methylene chloride and dimethylformamide. Scanning electron microscopy (SEM) images indicated that the fiber diameters and nanostructured morphologies of the electrospun membranes depended on the processing parameters, such as the solvent ratio and the polymer concentration. By adjusting both the solvent mixture ratio and the polymer concentration, we could fabricate uniform nanofiber non-woven membranes. Cell proliferation on the electrospun porous PLASB membranes was evaluated using mouse fibroblast cells; we compare these results with those of the cell responses on bulk PLASB films.
引用
收藏
页码:73 / 79
页数:7
相关论文
共 66 条
[1]   Recent developments in ring opening polymerization of lactones for biomedical applications [J].
Albertsson, AC ;
Varma, IK .
BIOMACROMOLECULES, 2003, 4 (06) :1466-1486
[2]   An overview of polylactides as packaging materials [J].
Auras, R ;
Harte, B ;
Selke, S .
MACROMOLECULAR BIOSCIENCE, 2004, 4 (09) :835-864
[3]   In vitro characterization and in vivo release profile of a poly(D,L-lactide-co-glycolide)-based implant delivery system for the α-MSH analog, melanotan-I [J].
Bhardwaj, R ;
Blanchard, J .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1998, 170 (01) :109-117
[4]   Electrospinning collagen and elastin: Preliminary vascular tissue engineering [J].
Boland, ED ;
Matthews, JA ;
Pawlowski, KJ ;
Simpson, DG ;
Wnek, GE ;
Bowlin, GL .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2004, 9 :1422-1432
[5]   Tailoring tissue engineering scaffolds using electrostatic processing techniques: A study of poly(glycolic acid) electrospinning [J].
Boland, ED ;
Wnek, GE ;
Simpson, DG ;
Pawlowski, KJ ;
Bowlin, GL .
JOURNAL OF MACROMOLECULAR SCIENCE-PURE AND APPLIED CHEMISTRY, 2001, 38 (12) :1231-1243
[6]   Novel graft PLLA-based copolymers: Potential of their application to particle technology [J].
Calandrelli, L ;
De Rosa, G ;
Errico, ME ;
La Rotonda, MI ;
Laurienzo, P ;
Malinconico, M ;
Oliva, A ;
Quaglia, F .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 2002, 62 (02) :244-253
[7]   Effects of the rate of solvent evaporation on the characteristics of drug loaded PLLA and PDLLA microspheres [J].
Chung, TW ;
Huang, YY ;
Liu, YZ .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2001, 212 (02) :161-169
[8]   New catalysts for poly(butylene terephthalate) synthesis. Part 3: Effect of phosphate co-catalysts [J].
Colonna, M ;
Banach, TE ;
Berti, C ;
Fiorini, M ;
Marianucci, E ;
Messori, M ;
Pilati, F ;
Toselli, M .
POLYMER, 2003, 44 (17) :4773-4779
[9]   Beaded nanofibers formed during electrospinning [J].
Fong, H ;
Chun, I ;
Reneker, DH .
POLYMER, 1999, 40 (16) :4585-4592
[10]   Controlling the fiber diameter during electrospinning [J].
Fridrikh, SV ;
Yu, JH ;
Brenner, MP ;
Rutledge, GC .
PHYSICAL REVIEW LETTERS, 2003, 90 (14) :4