Properties of collagen/chitosan scaffolds for skin tissue engineering
Keywords:
Collagen, Chitosan, Fibroblast, Scaffold, Skin tissue engineeringAbstract
Biopolymer blends between collagen and chitosan have the potential to produce cell scaffolds with biocompatible properties. In this study, porous scaffolds were fabricated by freeze drying the solution of collagen and chitosan and crosslinked by dehydrothermal treatment (DHT). Various types of scaffolds were prepared by varying compositions of collagen and chitosan. The scaffolds were fully characterized by Fourier transform infrared (FT-IR) spectroscopy. The results proved that collagen and chitosan scaffolds in all blending compositions contained only physical but not chemical interaction in molecular level. The compressive modulus from a universal mechanical testing machine decreased with increasing the compositions of chitosan. Equilibrium swelling ratios of approximately 6-8, carried out in phosphate buffered saline (PBS) at physiological pH (7.4) were found in case of collagen dominate scaffolds. The lysozyme biodegradation test demonstrated that the presence of chitosan could significantly prolong the biodegradation of collagen/chitosan scaffolds. The collagen/chitosan scaffold was more effective to promote and accelerate L929 cell proliferation, particularly for scaffolds containing 30% of chitosan. The results elucidated that the blends of collagen with chitosan have a high possibility to be applied as new materials for skin tissue engineering.Downloads
References
(1) Brouwer, J., Leeuwen-Herberts, T. and Ruit, M.O. 1984. Determination of lysozyme in serum, urine, cerebrospinal fluid and feces by enzyme immunoassay. Clinica Chimica Acta. 142 : 21-30.
(2) Chatelet, C., Damour, O. and Domard, A. 2001. Influence of the degree of acetylation on some biological properties of chitosan films. Biomaterials. 22 : 261-268.
(3) Howling, G. I., Dettmar, P. W., Goddard, P. A., Hampson, F.C., Dornish, M. and Wood, E.J. 2001. The effect of chitin and chitosan on the proliferation of human skin fibroblasts and keratinocytes in vitro. Biomaterials. 22 : 2959-2966.
(4) Kratz, G., Arnander, C., Swedenborg, J., Back, M., Falk, C. and Gouda, I. 1997. Heparinchitosan complexes stimulate wound healing in human skin. Scand J. Plast. Reconstr. Hand. Surg. 31 : 119-132.
(5) Kratz, G., Back, M., Arnander, C. and Larm, O.I. 1998. Immobilised heparin accelerates the healing of human wounds in vivo. Scand. J. Plast. Reconstr. Hand. Surg. 32 : 381-385.
(6) Ma, L., Gao, C.Y., Mao, Z.W., Shen, J.C. and Hu, X.Q. 2003. Collagen/chitosan porous scaffolds with improved biostability for skin tissue engineering. Biomaterials. 24 : 4833-4841.
(7) Mao, J. S., Cui, Y. L., Wang, X. H., Sun, Y., Zhao, H.M. and Yao, K.Y. 2004. A preliminary study on chitosan and gelatin polyelectrolyte complex cytocompatibility by cell cycle and apoptesis analysis. Biomaterials 25 : 3973-3981.
(8) Monal, W., Brugnerotto, J., Lizardi, J., Goycoolea, F.M., DesbrieÁres, J. and Rinaudo, M. 2001. An infrared investigation in relation with chitin and chitosan characterization. Polymer. 42 : 3569-3580.
(9) Mosmann, T. 1983. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J. Immunological Methods. 65 : 55-63.
(10) O’Brien, F.J., Harley, B.A., Yannas, I.V. and Gibson, L. 2004. Influence of freezing rate on pore structure in freeze dried collagenGAG scaffolds. Biomaterials. 25 : 1077- 1086.
(11) O’Brien, F.J., Harley, B.A., Yannas, I.V. and Gibson, L. 2005. The effect of pore size on cell adhesion in collagen-GAG scaffolds. Biomaterials. 26 : 433-441.
(12) Porstmann, B., Jung, K., Schmechta, H., Evers, U., Pergande, M. and Porstmann, T. 1989. Measurement of lysozyme in human body fluids: comparison of various enzyme immunoassay techniques and their diagnostic application. Clin Biochem. 22 : 349-355.
(13) Quirk, R. A., Chen, W. C., Davies, M. C., Tendler, S.J.B. and Shakesheff, K.M. 2001. Poly(l-lysine)–GRGDS as a biomimetic surface modifier for poly(lactic acid).Biomaterials.22 : 865–872.
(14) Rinaudo, M., Milas, M. and Dung, P.L. 1993. Characterization of chitosan. Influence of ionic strength and degree of acetylation on chain expansion. Int. J. Biol. Macromol. 15 : 281-285.
(15) Schmidt, R., Chung, L., Andrews, A., Spyratou, O. and Turner, T. 1993. Biocompatibility of wound management products: a study of the effect of various polysaccharides on murine L929 fibroblast proliferation and macrophage respiratory burst. J. Pharm Pharmacol. 45 : 508-513.
(16) Shanmugasundaram, N., Ravichandran, P., Neelakanta, P.R., Ramamurty, N., Pal, S. and Rao, K.P. 2001. Collagen-chitosan polymeric scaffolds for the in vitro culture of human epidermoid carcinoma cells. Biomaterials. 22 : 1943-1951.
(17) Sionkowska, A., Wisniewski, M., Skopinska, J., Kennedy, C.J. and Wess, T.J. 2004. The photochemical stability of collagenchitosan blends. Biomaterials. 162 : 545– 554.
(18) Sundararajan, M. V. and Howard, M. 1999. Porous chitosan scaffolds for tissue engineering. Biomaterials. 20 : 1133-1142.
(19) Taravel, M.N. and Domard, A. 1996. Collagen and its interactions with chitosan, III. some biological and mechanical properties. Biomaterials. 17 : 451–455.
(20) Terbojevich, M., Cosani, A. and Muzzarelli, R.A.A. 1996. Molecular parameters of chitosans depolymerized with the aid of papain. Carbohydr. polym. 29 : 63-68.
(21) Wang, X. H., Li, D. P., Wang, W. J., Feng, Q.L., Cui, F.Z. and Xub, Y.X. 2003. Crosslinked collagen/chitosan matrix for artificial livers. Biomaterials. 24 : 3213– 3220.
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