Title of article :
Chitosan–RGDSGGC conjugate as a scaffold material for musculoskeletal tissue engineering
Author/Authors :
Tatsuya Masuko، نويسنده , , Norimasa Iwasaki، نويسنده , , Shintaro Yamane، نويسنده , , Tadanao Funakoshi، نويسنده , , Tokifumi Majima، نويسنده , , Akio Minami، نويسنده , , Noriko Ohsuga، نويسنده , , Takashi Ohta، نويسنده , , Shin-ichiro Nishimura، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2005
Pages :
9
From page :
5339
To page :
5347
Abstract :
In the present study, we have developed a novel and versatile method for the preparation of chitosan-peptide complex based on the selective reaction of chitosan with 2-iminothiolane. The new type of SH-chitosan derivative showed an excellent solubility to aqueous solution even in the alkaline conditions. This characteristic greatly facilitated further modification study of chitosan with a variety of bioactive substances. A synthetic peptide, RGDSGGC containing RGDS moiety that is known as one of the most important cell adhesive peptides, was readily coupled by disulfide bonds formation with sulfhydryl groups of SH-chitosan in the presence of dimethyl sulfoxide. Next, the effect of the introduction of RGDSGGC moiety to chitosan on cell adhesion and proliferation activity of chondrocytes and fibroblasts were evaluated. As a result, it was suggested that this polysaccharide-peptide conjugate exhibited excellent capacities for both cell adhesion and cell proliferation of chondrocytes and fibroblasts. Considering the growing importance of the biocompatible scaffolds in the recent tailored tissue engineering technique, these results indicate that the present strategy of 2-iminothiolane-based conjugation of polysaccharides with biologically active peptides will become a key and potential technology to develop desirable scaffold materials for the tissue regenerations.
Keywords :
Adhesion , Chondrocyte , fibroblast , Polysaccharide , peptide
Journal title :
Biomaterials
Serial Year :
2005
Journal title :
Biomaterials
Record number :
546375
Link To Document :
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