The Future of Carbon Dioxide for Polymer Processing in Tissue Engineering

被引:44
作者
Bhamidipati, Manjari [1 ]
Scurto, Aaron M. [1 ,2 ]
Detamore, Michael S. [1 ,2 ]
机构
[1] Univ Kansas, Bioengn Grad Program, Lawrence, KS 66045 USA
[2] Univ Kansas, Dept Chem & Petr Engn, Lawrence, KS 66045 USA
关键词
OSTEOCHONDRAL INTERFACE REGENERATION; SUPERCRITICAL-FLUID TECHNOLOGY; HIGH-PRESSURE RHEOLOGY; IN-VITRO; MECHANICAL-PROPERTIES; PHASE INVERSION; MACROSCOPIC GRADIENTS; POLY(L-LACTIC ACID); HYDROGEN-PEROXIDE; POROUS SCAFFOLDS;
D O I
10.1089/ten.teb.2012.0361
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The use of CO2 for scaffold fabrication in tissue engineering was popularized in the mid-1990s as a tool for producing polymeric foam scaffolds, but had fallen out of favor to some extent, in part due to challenges with pore interconnectivity. Pore interconnectivity issues have since been resolved by numerous dedicated studies that have collectively outlined how to control the appropriate parameters to achieve a pore structure desirable for tissue regeneration. In addition to CO2 foaming, several groups have leveraged CO2 as a swelling agent to impregnate scaffolds with drugs and other bioactive additives, and for encapsulation of plasmids within scaffolds for gene delivery. Moreover, in contrast to CO2 foaming, which typically relies on supercritical CO2 at very high pressures, CO2 at much lower pressures has also been used to sinter polymeric microspheres together in the presence of cells to create cell-seeded scaffolds in a single step. CO2 has a number of advantages for polymer processing in tissue engineering, including its ease of use, low cost, and the opportunity to circumvent the use of organic solvents. Building on these advantages, and especially now with the tremendous precedent that has paved the way in defining operating parameters, and making the technology accessible for new groups to adapt, we invite and encourage our colleagues in the field to leverage CO2 as a new tool to enhance their own respective unique capabilities.
引用
收藏
页码:221 / 232
页数:12
相关论文
共 108 条
[1]   The fabrication of elastin-based hydrogels using high pressure CO2 [J].
Annabi, Nasim ;
Mithieux, Suzanne M. ;
Weiss, Anthony S. ;
Dehghani, Fariba .
BIOMATERIALS, 2009, 30 (01) :1-7
[2]   Measurement and prediction of diffusion coefficients of supercritical CO2 in molten polymers [J].
Areerat, S ;
Funami, E ;
Hayata, Y ;
Nakagawa, D ;
Ohshima, M .
POLYMER ENGINEERING AND SCIENCE, 2004, 44 (10) :1915-1924
[3]   Carbon dioxide impregnation of electrospun polycaprolactone fibers [J].
Ayodeji, Olukemi ;
Graham, Emily ;
Kniss, Douglas ;
Lannutti, John ;
Tomasko, David .
JOURNAL OF SUPERCRITICAL FLUIDS, 2007, 41 (01) :173-178
[4]   Structure and mechanical properties of supercritical carbon dioxide processed porous resorbable polymer constructs [J].
Baker, K. C. ;
Bellair, R. ;
Manitiu, M. ;
Herkowitz, H. N. ;
Kannan, R. M. .
JOURNAL OF THE MECHANICAL BEHAVIOR OF BIOMEDICAL MATERIALS, 2009, 2 (06) :620-626
[5]  
Barry JJA, 2006, PHILOS T R SOC A, V364, P249, DOI [10.1098/rsta.2005.1687, 10.1098/rsta.2000.1687]
[6]   Porous methacrylate scaffolds: supercritical fluid fabrication and in vitro chondrocyte responses [J].
Barry, JJA ;
Gidda, HS ;
Scotchford, CA ;
Howdle, SM .
BIOMATERIALS, 2004, 25 (17) :3559-3568
[7]   Tissue-engineered bone formation in vivo using a novel sintered polymeric microsphere matrix [J].
Borden, M ;
Attawia, M ;
Khan, Y ;
El-Amin, SE ;
Laurencin, CT .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 2004, 86B (08) :1200-1208
[8]  
Butler R, 2001, ADV MATER, V13, P1459, DOI 10.1002/1521-4095(200110)13:19<1459::AID-ADMA1459>3.0.CO
[9]  
2-K
[10]   Sterilization of biological pathogens using supercritical fluid carbon dioxide containing water and hydrogen peroxide [J].
Checinska, Aleksandra ;
Fruth, Ingrid A. ;
Green, Tonia L. ;
Crawford, Ronald L. ;
Paszczynski, Andrzej J. .
JOURNAL OF MICROBIOLOGICAL METHODS, 2011, 87 (01) :70-75