Influence of macromer molecular weight and chemistry on poly(β-amino ester) network properties and initial cell interactions

被引:47
作者
Brey, Darren M. [1 ]
Erickson, Isaac [1 ]
Burdick, Jason A. [1 ]
机构
[1] Univ Penn, Dept Bioengn, Philadelphia, PA 19104 USA
关键词
polymers; degradable; photopolymerization; poly(beta-amino ester); tissue engineering;
D O I
10.1002/jbm.a.31494
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A library of photocrosslinkable poly(beta-amino ester)s (PBAEs) was recently synthesized to expand the number of degradable polymers that can be screened and developed for a variety of biological applications. In this work, the influence of variations in macromer chemistry and macromer molecular weight (MMW) on network reaction behavior, overall bulk properties, and cell interactions were investigated. The MMW was controlled through alterations in the initial diacrylate to amine ratio (>= 1) during synthesis and decreased with an increase in this ratio. Lower MMWs reacted more quickly and to higher double bond conversions than higher MMWs, potentially due to the higher concentration of reactive groups. Additionally, the lower MMWs led to networks with 'higher compressive and tensile moduli that degraded slower than networks formed from higher MMWs because of an increase in the crosslinking density and decrease in the number of degradable units per crosslink. The adhesion and spreading of osteoblast-like cells on polymer films was found to be dependent on both the macromer chemistry and the MMW. In general, the number of cells was similar on networks formed from a range of MMWs, but the spreading was dramatically influenced by MMW (higher spreading with lower MMWs). These results illustrate further diversity in photocrosslinkable PBAE properties and that the chemistry and macromer structure must be carefully selected for the desired application. (C) 2007 Wiley Periodicals, Inc.
引用
收藏
页码:731 / 741
页数:11
相关论文
共 39 条
[1]  
Agrawal CM, 2001, J BIOMED MATER RES, V55, P141, DOI 10.1002/1097-4636(200105)55:2<141::AID-JBM1000>3.0.CO
[2]  
2-J
[3]   Parallel synthesis and biophysical characterization of a degradable polymer library for gene delivery [J].
Akinc, A ;
Lynn, DM ;
Anderson, DG ;
Langer, R .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (18) :5316-5323
[4]   Probing the role of multicellular organization in three-dimensional microenvironments [J].
Albrecht, DR ;
Underhill, GH ;
Wassermann, TB ;
Sah, RL ;
Bhatia, SN .
NATURE METHODS, 2006, 3 (05) :369-375
[5]   A combinatorial library of photocrosslinkable and degradable materials [J].
Anderson, Daniel G. ;
Tweedie, Catherine A. ;
Hossain, Naushad ;
Navarro, Sergio M. ;
Brey, Darren M. ;
Van Vliet, Krystyn J. ;
Langer, Robert ;
Burdick, Jason A. .
ADVANCED MATERIALS, 2006, 18 (19) :2614-+
[6]   Photopolymerizable degradable polyanhydrides with osteocompatibility [J].
Anseth, KS ;
Shastri, VR ;
Langer, R .
NATURE BIOTECHNOLOGY, 1999, 17 (02) :156-159
[7]   In situ forming degradable networks and their application in tissue engineering and drug delivery [J].
Anseth, KS ;
Metters, AT ;
Bryant, SJ ;
Martens, PJ ;
Elisseeff, JH ;
Bowman, CN .
JOURNAL OF CONTROLLED RELEASE, 2002, 78 (1-3) :199-209
[8]   The influence of comonomer composition on dimethacrylate resin properties for dental composites [J].
Anseth, KS ;
Goodner, MD ;
Reill, MA ;
Kannurpatti, AR ;
Newman, SM ;
Bowman, CN .
JOURNAL OF DENTAL RESEARCH, 1996, 75 (08) :1607-1612
[9]   New directions in photopolymerizable biomaterials [J].
Anseth, KS ;
Burdick, JA .
MRS BULLETIN, 2002, 27 (02) :130-136
[10]   Microfluidic tectonics: A comprehensive construction platform for microfluidic systems [J].
Beebe, DJ ;
Moore, JS ;
Yu, Q ;
Liu, RH ;
Kraft, ML ;
Jo, BH ;
Devadoss, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (25) :13488-13493