Porous poly(ethylene glycol)-polyurethane hydrogels as potential biomaterials

被引:26
作者
Divakaran, Anumon V. [1 ]
Torris, Arun A. T. [1 ]
Lele, Ashish K. [1 ]
Badiger, Manohar V. [1 ]
机构
[1] CSIR Natl Chem Lab, Polymer Sci & Engn Div, Pune 411008, Maharashtra, India
关键词
hydrogels; poly(ethylene glycol); polyurethane; porosity; permeability; SUPERCRITICAL CARBON-DIOXIDE; CELL-GROWTH; PORE-SIZE; SUPERABSORBENT HYDROGELS; STATISTICAL-MECHANICS; OSTEOCHONDRAL DEFECTS; ALCOHOL HYDROGELS; POLYMER SCAFFOLDS; RABBIT KNEE; TISSUE;
D O I
10.1002/pi.4802
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We report the synthesis of porous poly(ethylene glycol)-polyurethane (PEG-PU) hydrogels using PEG-4000 as a soft segment and 4,4-methylenebis(cyclohexylisocyanate) as a hard segment. The degree of swelling in the hydrogels could be controlled by varying the amount of crosslinking agent, namely 1,2,6-hexanetriol. Structural characterization of the hydrogels was performed using solid-state C-13 NMR and Fourier transform infrared spectroscopy. Wide-angle X-ray diffraction studies revealed the existence of crystalline domains of PEG and small-angle X-ray scattering studies showed the presence of lamellar microstructures. For generating a porous structure in the hydrogels, cryogenic treatment with lyophilization was used. Scanning electron microscopy and three-dimensional micro-computed tomography imaging of the hydrogels indicated the presence of interconnected pores. The mechanical strength of the hydrogels and xerogels was measured using dynamic mechanical analysis. The observed dynamic storage moduli (E) for the equilibrium swollen and dry gels were found to be 0.15 and 4.2 MPa, respectively. Interestingly, the porous PEG-PU xerogel also showed E of 5.6 MPa indicating a similar mechanical strength upon incorporating porosity into the gel matrix. Finally, preliminary cytocompatibility studies showed the ability of cells to proliferate in the hydrogels. These gels show promise for applications as scaffolds and implants in tissue engineering. (c) 2014 Society of Chemical Industry
引用
收藏
页码:397 / 404
页数:8
相关论文
共 64 条
[1]  
Annabi N, 2010, TISSUE ENG PART B-RE, V16, P371, DOI [10.1089/ten.teb.2009.0639, 10.1089/ten.TEB.2009.0639]
[2]   Stereolithography of three-dimensional bioactive poly(ethylene glycol) constructs with encapsulated cells [J].
Arcaute, Karina ;
Mann, Brenda K. ;
Wicker, Ryan B. .
ANNALS OF BIOMEDICAL ENGINEERING, 2006, 34 (09) :1429-1441
[3]   Host response to tissue engineered devices [J].
Babensee, JE ;
Anderson, JM ;
McIntire, LV ;
Mikos, AG .
ADVANCED DRUG DELIVERY REVIEWS, 1998, 33 (1-2) :111-139
[4]   POROGENS IN THE PREPARATION OF MICROPOROUS HYDROGELS BASED ON POLY(ETHYLENE OXIDES) [J].
BADIGER, MV ;
MCNEILL, ME ;
GRAHAM, NB .
BIOMATERIALS, 1993, 14 (14) :1059-1063
[5]   Swelling kinetics of a hydrogel of poly(ethylene glycol) and poly(acrylamide-co-styrene) [J].
Bajpai, AK ;
Shrivastava, M .
JOURNAL OF APPLIED POLYMER SCIENCE, 2002, 85 (07) :1419-1428
[6]  
Barry JJA, 2006, PHILOS T R SOC A, V364, P249, DOI [10.1098/rsta.2005.1687, 10.1098/rsta.2000.1687]
[7]   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
[8]   Photo-patterning of porous hydrogels for tissue engineering [J].
Bryant, Stephanie J. ;
Cuy, Janet L. ;
Hauch, Kip D. ;
Ratner, Buddy D. .
BIOMATERIALS, 2007, 28 (19) :2978-2986
[9]  
Buchholz F.L., 1994, SUPERABSORBENT POLYM
[10]   Semisynthetic resorbable materials from hyaluronan esterification [J].
Campoccia, D ;
Doherty, P ;
Radice, M ;
Brun, P ;
Abatangelo, G ;
Williams, DF .
BIOMATERIALS, 1998, 19 (23) :2101-2127