Real-time in situ rheology of alginate hydrogel photocrosslinking

被引:100
作者
Bonino, Christopher A. [1 ]
Samorezov, Julia E. [2 ]
Jeon, Oju [2 ]
Alsberg, Eben [2 ,3 ]
Khan, Saad A. [1 ]
机构
[1] N Carolina State Univ, Dept Chem & Biomol Engn, Raleigh, NC 27695 USA
[2] Case Western Reserve Univ, Dept Biomed Engn, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Dept Orthopaed Surg, Cleveland, OH 44106 USA
关键词
THIOL-ENE POLYMERS; MECHANICAL-PROPERTIES; GEL POINT; PHOTOINITIATED POLYMERIZATION; UV; BIOMATERIALS; DEGRADATION; CELLS; CYTOCOMPATIBILITY; GLUTARALDEHYDE;
D O I
10.1039/c1sm06109g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
The reaction dynamics of biodegradable, photocrosslinkable sodium alginate hydrogels are studied by in situ, dynamic rheology. Alginate, chemically-modified with methacrylate groups, crosslinks by ultraviolet (UV) light exposure in the presence of a photoinitiator. The gel formation is monitored during UV irradiation from a light emitting diode (LED) bottom plate fixture on the rheometer. Material properties of the hydrogels, including gel points and relaxation exponent, are evaluated using the Winter-Chambon criteria. We also report a new, complementary empirical method for determining the gel point from the reduction in sample strain at the onset of gelation, via monitoring the strain curve. In addition, the crosslinking dynamics and hydrogel moduli are altered by changing the UV irradiation intensities (3-15 mW cm(-2)) and degree of methacrylation (5-25%). Dynamic rheological measurements of hydrogels as described in this paper are a potentially powerful tool to elucidate the dynamics of gelation and predict mechanical properties. This technique may aid in the design of polymer formulations with light-reactive chemical species, which have tunable properties that can be matched to a range of applications, including regenerative medicine.
引用
收藏
页码:11510 / 11517
页数:8
相关论文
共 48 条
[1]
Craniofacial tissue engineering [J].
Alsberg, E ;
Hill, EE ;
Mooney, DJ .
CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE, 2001, 12 (01) :64-75
[2]
Regulating bone formation via controlled scaffold degradation [J].
Alsberg, E ;
Kong, HJ ;
Hirano, Y ;
Smith, MK ;
Albeiruti, A ;
Mooney, DJ .
JOURNAL OF DENTAL RESEARCH, 2003, 82 (11) :903-908
[3]
Mechanical properties of hydrogels and their experimental determination [J].
Anseth, KS ;
Bowman, CN ;
BrannonPeppas, L .
BIOMATERIALS, 1996, 17 (17) :1647-1657
[4]
Cytotoxicity of photosensitizers camphorquinone and 9-fluorenone with visible light irradiation on a human submandibular-duct cell line in vitro [J].
Atsumi, T ;
Murata, J ;
Kamiyanagi, I ;
Fujisawa, S ;
Ueha, T .
ARCHIVES OF ORAL BIOLOGY, 1998, 43 (01) :73-81
[5]
Toward an Enhanced Understanding and Implementation of Photopolymerization Reactions [J].
Bowman, Christopher N. ;
Kloxin, Christopher J. .
AICHE JOURNAL, 2008, 54 (11) :2775-2795
[6]
Cytocompatibility of UV and visible light photoinitiating systems on cultured NIH/3T3 fibroblasts in vitro [J].
Bryant, SJ ;
Nuttelman, CR ;
Anseth, KS .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2000, 11 (05) :439-457
[7]
Conversion and temperature profiles during the photoinitiated polymerization of thick orthopaedic biomaterials [J].
Burdick, JA ;
Peterson, AJ ;
Anseth, KS .
BIOMATERIALS, 2001, 22 (13) :1779-1786
[8]
Buschow K. H. J., 2001, PHYS CHEM GELATION, V5, P6991
[9]
Structural and rheological evolution of silica nanoparticle gels [J].
Cao, X. J. ;
Cummins, H. Z. ;
Morris, J. F. .
SOFT MATTER, 2010, 6 (21) :5425-5433
[10]
Photopolymerized thermosensitive hydrogels for tailorable diffusion-controlled protein delivery [J].
Censi, R. ;
Vermonden, T. ;
van Steenbergen, M. J. ;
Deschout, H. ;
Braeckmans, K. ;
De Smedt, S. C. ;
van Nostrum, C. F. ;
di Martino, P. ;
Hennink, W. E. .
JOURNAL OF CONTROLLED RELEASE, 2009, 140 (03) :230-236