Nonionic polymer cross-linked chitosan hydrogel: Preparation and bioevaluation

Journal of Biomaterials Science, Polymer Edition

Volumn 24, Issue 13, 2013, Pages 1564-1574

  Xu, Liangxin ^a   Zhang, Xiaoyong ^a   Zhu, Chongyu ^a   Zhang, Yaling ^a   Fu, Changkui ^a   Yang, Bin ^a   Tao, Lei ^a   Wei, Yen ^a  

^a TSINGHUA UNIVERSITY   (China)

Author keywords

biocompatibility; chitosan; hydrogel; physical blending; polyacrylamide

Indexed keywords

BIOMEDICAL APPLICATIONS; CROSS LINKED CHITOSAN; HEMOCOMPATIBILITY; NONIONIC POLYMERS; PHYSICAL BLENDING; ROOM TEMPERATURE; SCANNING ELECTRON MICROSCOPY IMAGE; STRAIGHT-FORWARD METHOD;

BIOCOMPATIBILITY; BIOLOGICAL MATERIALS; BLOOD; CELL MEMBRANES; CHITOSAN; CROSSLINKING; CYTOLOGY; DERIVATIVES; MEDICAL APPLICATIONS; POLYACRYLATES; SCANNING ELECTRON MICROSCOPY;

HYDROGELS;

AMINE; CHITOSAN; POLYACRYLAMIDE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BIOCOMPATIBILITY; CELL MEMBRANE; CELL STRUCTURE; CONTROLLED STUDY; CROSS LINKING; CYTOTOXICITY; ERYTHROCYTE; ERYTHROCYTE SHAPE; FLOW KINETICS; HEMOLYSIS; HUMAN; HUMAN CELL; HYDROGEL; MALE; NONHUMAN; PRIORITY JOURNAL; RAT; ROOM TEMPERATURE; SCANNING ELECTRON MICROSCOPY;

ACRYLIC RESINS; ADSORPTION; ANIMALS; BIOCOMPATIBLE MATERIALS; CELL LINE; CHITOSAN; CROSS-LINKING REAGENTS; HELA CELLS; HEMOLYSIS; HUMANS; MALE; MATERIALS TESTING; RATS; RATS, WISTAR; RHEOLOGY;

EID: 84880459093     PISSN: 09205063     EISSN: 15685624     Source Type: Journal    
DOI: 10.1080/09205063.2013.781934     Document Type: Article

References (45)

1. Kumar M. A review of chitin and chitosan applications. React. Funct. Polym. 2000;46:1-27.
2. Ong SY, Wu J, Moochhala SM, Tan MH, Lu J. Development of a chitosan-based wound dressing with improved hemostatic and antimicrobial properties. Biomaterials. 2008;29:4323-4332.
3. Dai C, Liu C, Wei J, Hong H, Zhao Q. Molecular imprinted macroporous chitosan coated mesoporous silica xerogels for hemorrhage control. Biomaterials. 2010;31:7620-7630.
4. Dowling MB, Kumar R, Keibler MA, Hess JR, Bochicchio GV, Raghavan SR. A self-assembling hydrophobically modified chitosan capable of reversible hemostatic action. Biomaterials. 2011;32:3351-3357.
5. Pusateri AE, McCarthy SJ, Gregory KW, Harris RA, Cardenas L, McManus AT, Goodwin CW. Effect of a chitosan-based hemostatic dressing on blood loss and survival in a model of severe venous hemorrhage and hepatic injury in swine. J. Trauma. 2003;54:177-182.
6. Hattori H, Amano Y, Nogami Y, Takase B, Ishihara M. Hemostasis for severe hemorrhage with photocrosslinkable chitosan hydrogel and calcium alginate. Ann. Biomed. Eng. 2010;38:3724-3732.
7. De Castro GP, Dowling MB, Kilbourne M, Keledjian K, Driscoll IR, Raghavan SR, Hess JR, Scalea TM, Bochicchio GV. Determination of efficacy of novel modified chitosan sponge dressing in a lethal arterial injury model in swine. J. Trauma Acute Care Surg. 2012;72:899-907.
8. Gu R, Sun W, Zhou H, Wu Z, Meng Z, Zhu X, Tang Q, Dong J, Dou G. The performance of a fly-larva shell-derived chitosan sponge as an absorbable surgical hemostatic agent. Biomaterials. 2010;31:1270-1277.
9. Sashiwa H, Aiba S. Chemically modified chitin and chitosan as biomaterials. Prog. Polym. Sci. 2004;29:887-908.
10. Pillai C, Paul W, Sharma CP. Chitin and chitosan polymers: chemistry, solubility and fiber formation. Prog. Polym. Sci. 2009;34:641-678.
11. Kumar M, Muzzarelli RAA, Muzzarelli C, Sashiwa H, Domb AJ. Chitosan chemistry and pharmaceutical perspectives. Chem. Rev. 2004;104:6017-6084.
12. Rinaudo M. Chitin and chitosan: properties and applications. Prog. Polym. Sci. 2006;31:603-632.
13. Muzzarelli RAA. Chitins and chitosans for the repair of wounded skin, nerve, cartilage and bone. Carbohydr. Polym. 2009;76:167-182.
14. Sa-Lima H, Caridade SG, Mano JF, Reis RL. Stimuli-responsive chitosan-starch injectable hydrogels combined with encapsulated adipose-derived stromal cells for articular cartilage regeneration. Soft Matter. 2010;6:5184-5195.
15. Li X, Ma XX, Fan DD, Zhu CH. New suitable for tissue reconstruction injectable chitosan/collagen- based hydrogels. Soft Matter. 2012;8:3781-3790.
16. Aliaghaie M, Mirzadeh H, Dashtimoghadam E, Taranejoo S. Investigation of gelation mechanism of an injectable hydrogel based on chitosan by rheological measurements for a drug delivery application. Soft Matter. 2012;8:3128-3137.
17. Valmikinathan CM, Mukhatyar VJ, Jain A, Karumbaiah L, Dasari M, Bellamkonda RV. Photocrosslinkable chitosan based hydrogels for neural tissue engineering. Soft Matter. 2012;8:1964-1976.
18. Risbud MV, Bhonde RR. Polyacrylamide-chitosan hydrogels: in vitro biocompatibility and sustained antibiotic release studies. Drug Delivery. 2000;7:69-75.
19. Berger J, Reist M, Mayer J, Felt O, Gurny R. Structure and interactions in chitosan hydrogels formed by complexation or aggregation for biomedical applications. Eur. J. Pharm. Biopharm. 2004;57:35-52.
20. Berger J, Reist M, Mayer J, Felt O, Peppas N, Gurny R. Structure and interactions in covalently and ionically crosslinked chitosan hydrogels for biomedical applications. Eur. J. Pharm. Biopharm. 2004;57:19-34.
21. Zhang Y, Tao L, Li S, Wei Y. Synthesis of multi-responsive and dynamic chitosan-based hydrogels for controlled release of bioactive molecules. Biomacromolecules. 2011;12:2894-2901.
22. Yang B, Zhang Y, Zhang X, Tao L, Li S, Wei Y. Facilely prepared inexpensive and biocompatible selfhealing hydrogel: a new injectable cell therapy carrier. Polym. Chem. 2012;3:3235-3238.
23. Anirudhan T, Sandeep S. Synthesis and characterization of molecularly imprinted polymer of Nmaleoylchitosan- grafted-2-acrylamido-2- methylpropanesulfonic acid and its controlled delivery and recognition of bovine serum albumin. Polym. Chem. 2011;2:2052-2061.
24. Xin Y, Yuan J. Schiff's base as a stimuli-responsive linker in polymer chemistry. Polym. Chem. 2012;3:3045-3055.
25. Messing R, Schmidt AM. Perspectives for the mechanical manipulation of hybrid hydrogels. Polym. Chem. 2010;2:18-32.
26. Kim SK, Rajapakse N. Enzymatic production and biological activities of chitosan oligosaccharides (COS): a review. Carbohydr. Polym. 2005;62:357-368.
27. Brack H, Tirmizi S, Risen W. A spectroscopic and viscometric study of the metal ion-induced gelation of the biopolymer chitosan. Polymer. 1997;38:2351-2362.
28. Denuziere A, Ferrier D, Damour O, Domard A. Chitosan-chondroitin sulfate and chitosan-hyaluronate polyelectrolyte complexes: biological properties. Biomaterials. 1998;19:1275-1285.
29. Dambies L, Vincent T, Domard A, Guibal E. Preparation of chitosan gel beads by ionotropic molybdate gelation. Biomacromolecules. 2001;2:1198-1205.
30. Shu X, Zhu K. Controlled drug release properties of ionically cross-linked chitosan beads: the influence of anion structure. Int. J. Pharm. 2002;233:217-225.
31. Mao J, Cui Y, Wang X, Sun Y, Yin Y, Zhao H, Yao K. A preliminary study on chitosan and gelatin polyelectrolyte complex cytocompatibility by cell cycle and apoptosis analysis. Biomaterials. 2004;25:3973-3981.
32. Boddohi S, Moore N, Johnson PA, Kipper MJ. Polysaccharide-based polyelectrolyte complex nanoparticles from chitosan, heparin, and hyaluronan. Biomacromolecules. 2009;10:1402-1409.
33. Jiang T, Zhang Z, Zhou Y, Liu Y, Wang Z, Tong H, Shen X, Wang Y. Surface functionalization of titanium with chitosan/gelatin via electrophoretic deposition: characterization and cell behavior. Biomacromolecules 2010;11:1254-1260.
34. Bhat KA, Rajangam P, Dharmalingam S. The effect of chlorotrimethylsilane on bonding of nano hydroxyapatite with a chitosan-polyacrylamide matrix. Carbohydr. Res. 2012;352:143-150.
35. Cascone M, Maltinti S, Barbani N, Laus M. Effect of chitosan and dextran on the properties of poly (vinyl alcohol) hydrogels. J. Mater. Sci. - Mater. Med. 1999;10:431-435.
36. Noble L, Gray AI, Sadiq L, Uchegbu IF. A non-covalently cross-linked chitosan based hydrogel. Int. J. Pharm. 1999;192:173-182.
37. Richardson TP, Peters MC, Ennett AB, Mooney DJ. Polymeric system for dual growth factor delivery. Nat. Biotechnol. 2001;19:1029-1034.
38. Cerchiara T, Luppi B, Bigucci F, Orienti I, Zecchi V. Physically cross-linked chitosan hydrogels as topical vehicles for hydrophilic drugs. J. Pharm. Pharmacol. 2002;54:1453-1459.
39. Martin L, Wilson CG, Koosha F, Uchegbu IF. Sustained buccal delivery of the hydrophobic drug denbufylline using physically cross-linked palmitoyl glycol chitosan hydrogels. Eur. J. Pharm. Biopharm. 2003;55:35-45.
40. Ladet S, David L, Domard A. Multi-membrane hydrogels. Nature. 2008;452:76-79.
41. Dash M, Chiellini F, Ottenbrite R, Chiellini E. Chitosan - A versatile semi-synthetic polymer in biomedical applications. Prog. Polym. Sci. 2011;36:981-1014.
42. Zhang X, Hu W, Li J, Tao L, Wei Y. A comparative study of cellular uptake and cytotoxicity of multi-walled carbon nanotube, graphene oxide, and nanodiamond. Toxicol. Res. 2012;1:62-68.
43. Zhang X, Wang S, Fu C, Feng L, Ji Y, Tao L, Li S, Wei Y. PolyPEGylated nanodiamond for intracellular delivery of chemotherapeutic drug. Polym. Chem. 2012;3:2716-2719.
44. Zhang X, Wang S, Xu L, Ji Y, Feng L, Tao L, Li S, Wei Y. Biocompatible polydopamine fluorescent organic nanoparticles: facile preparation and cell imaging. Nanoscale. 2012;4:5581-5584.
45. Zhang X, Yin J, Peng C, Hu W, Zhu Z, Li W, Fan C, Huang Q. Distribution and biocompatibility studies of graphene oxide in mice after intravenous administration. Carbon. 2011;49:986-995.