Methacrylated glycol chitosan as a photopolymerizable biomaterial

被引:153
作者
Amsden, Brian G. [1 ]
Sukarto, Abby [1 ]
Knight, Darryl K. [1 ]
Shapka, Stephen N. [1 ]
机构
[1] Queens Univ, Dept Chem Engn, Kingston, ON K7L 3N6, Canada
关键词
D O I
10.1021/bm700691e
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glycol chitosan is a derivative of chitosan that is soluble at neutral pH and possesses potentially useful biological properties. With the goal of obtaining biocompatible hydrogels for use as tissue engineering scaffolds or drug delivery depots, glycol chitosan was converted to a photopolymerizable prepolymer through graft methacrylation using glycidyl methacrylate in aqueous media at pH 9. N-Methacrylation was verified by both H-1 NMR and C-13 NMR. The degree of N-methacrylation, measured via H-1 NMR, was easily varied from 1.5% to approximately 25% by varying the molar ratio of glycidyl methacrylate to glycol chitosan and the reaction time. Using a chondrocyte cell line, the N-methacrylated glycol chitosan was found to be noncytotoxic up to a concentration of 1 mg/mL. The prepolymer was cross-linked in solution using UV light and Irgacure 2959 photoinitiator under various conditions to yield gels of low sol content (similar to 5%), high equilibrium water content (85-95%), and thicknesses of up to 6 mm. Cross-polarization magic-angle spinning C-13 solid state NMR verified the complete conversion of the double bonds in the gel. Chondrocytes seeded directly onto the gel surface, populated the entirety of the gel and remained viable for up to one week. The hydrogels degraded slowly in vitro in the presence of lysozyme at a rate that increased as the cross-link density of the gels decreased.
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页码:3758 / 3766
页数:9
相关论文
共 56 条
[1]   REACTION OF CELLULOSE-POLY(GLYCIDYL METHACRYLATE) WITH METHYLAMINE [J].
ABOSHOSHA, MHH ;
IBRAHIM, NAE .
ANGEWANDTE MAKROMOLEKULARE CHEMIE, 1987, 152 :93-106
[2]   Intraarterial protein delivery via intimally-adherent bilayer hydrogels [J].
An, YJ ;
Hubbell, JA .
JOURNAL OF CONTROLLED RELEASE, 2000, 64 (1-3) :205-215
[3]   Effect of water-soluble reduced chitosan on Streptococcus mutans, plaque regrowth and biofilm vitality [J].
Bae, K. ;
Jun, E. J. ;
Lee, S. M. ;
Paik, D. I. ;
Kim, J. B. .
CLINICAL ORAL INVESTIGATIONS, 2006, 10 (02) :102-107
[4]   A method to protect sensitive molecules from a light-induced polymerizing environment [J].
Baroli, B ;
Shastri, VP ;
Langer, R .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2003, 92 (06) :1186-1195
[5]  
BOURKE SL, 2003, AAPS PHARM SCI, V5
[6]   Synthesis and characterization of photopolymerized multifunctional hydrogels: Water-soluble poly(vinyl alcohol) and chondroitin sulfate macromers for chondrocyte encapsulation [J].
Bryant, SJ ;
Davis-Arehart, KA ;
Luo, N ;
Shoemaker, RK ;
Arthur, JA ;
Anseth, KS .
MACROMOLECULES, 2004, 37 (18) :6726-6733
[7]   Delivery of osteoinductive growth factors from degradable PEG hydrogels influences osteoblast differentiation and mineralization [J].
Burdick, JA ;
Mason, MN ;
Hinman, AD ;
Thorne, K ;
Anseth, KS .
JOURNAL OF CONTROLLED RELEASE, 2002, 83 (01) :53-63
[8]   Evaluation of the biological properties of soluble chitosan and chitosan microspheres [J].
CarrenoGomez, B ;
Duncan, R .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1997, 148 (02) :231-240
[9]  
Cha SY, 2001, J POLYM SCI POL CHEM, V39, P880, DOI 10.1002/1099-0518(20010315)39:6<880::AID-POLA1062>3.0.CO
[10]  
2-K