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2017 | 22 | 82-96

Article title

SYNTHESIS AND POTENTIAL CYTOTOXICITY EVALUATION OF CARBOXYMETHYL CHITOSAN HYDROGELS

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EN

Abstracts

EN
The aim of the research was to employ radiation to produce flexible carboxymethyl chitosan (CMCS) based hydrogels of uniform structure to characterise their swelling properties and cytocompatibility for potential applications as hydrogel wound dressings. CMCS in aqueous solution was irradiated with an electron beam in the presence of a poly(ethylene glycol) diacrylate (PEGDA) macromonomer as a crosslinker, at 12 different compositions, i.e. 3–20% CMCS, 3 and 5% PEGDA. The obtained hydrogels were subjected to sol–gel analysis. The amount of insoluble fraction (up to 100%) rose with an increase in the PEGDA/polysaccharide ratio. Moreover, the equilibrium degree of swelling, ca. 15 to 200 g of water per g of gel, which was higher for lower content of crosslinker, decreased with the delivered dose, which was associated with an increase in crosslinking density. The in vitro XTT cell viability assay (murine fibroblasts, L929 cell line) showed no significant cytotoxicity of CMCS gels.

Contributors

  • Department of Experimental Surgery, Faculty of Medicine, Medical University of Lodz, Pabianicka 62, 93-513 Lodz, Poland
  • Department of Pharmaceutical Chemistry, Drug Analysis and Radiopharmacy, Faculty of Pharmacy, Medical University of Lodz, Muszyńskiego 1, 90-151 Lodz, Poland
  • Institute of Applied Radiation Chemistry, Faculty of Chemistry, Lodz University of Technology, Wroblewskiego 15, 93-590 Lodz, Poland.
  • Institute of Applied Radiation Chemistry, Faculty of Chemistry, Lodz University of Technology, Wroblewskiego 15, 93-590 Lodz, Poland.
  • Institute of Applied Radiation Chemistry, Faculty of Chemistry, Lodz University of Technology, Wroblewskiego 15, 93-590 Lodz, Poland.
  • Department of Pharmaceutical Chemistry, Drug Analysis and Radiopharmacy, Faculty of Pharmacy, Medical University of Lodz, Muszyńskiego 1, 90-151 Lodz, Poland
  • Institute of Applied Radiation Chemistry, Faculty of Chemistry, Lodz University of Technology, Wroblewskiego 15, 93-590 Lodz, Poland.

References

  • [1] Rosiak J, Rucinska-Rybus A, Pekala W; (1989) Method of manufacturing hydrogel dressings. US patent 4,871,490, Polish patent 151,581.
  • [2] Wach RA, Kudoh H, Zhai M, Nagasawa N, Muroya Y, Yoshii F, Katsumura Y; (2004) Rate constants of reactions of carboxymethylcellulose with hydrated electron, hydroxyl radical and the decay of CMC macroradicals. A pulse radiolysis study. Polymer 45(24), 8165–8171. DOI:10.1016/j.polymer.2004.09.086
  • [3] Wach RA, Mitomo H, Yoshii F, Kume T; (2001) Hydrogel of biodegradable cellulose derivatives. II. Effect of some factors on radiation-induced crosslinking of CMC. Journal of Applied Polymer Science 81(12), 3030–3037. DOI:10.1002/app.1753
  • [4] Wach RA, Rokita B, Bartoszek N, Katsumura Y, Ulanski P, Rosiak JM; (2014) Hydroxyl radical-induced crosslinking and radiation-initiated hydrogel formation in dilute aqueous solutions of carboxymethylcellulose. Carbohydrate Polymers 112, 412–415. DOI:10.1016/j.carbpol.2014.06.007
  • [5] Muzzarelli RAA; (1988) Carboxymethylated chitins and chitosans. Carbohydrate Polymers 8(1), 1–21. DOI:10.1016/0144-8617(88)90032-X
  • [6] Li Y-S, Han Y, Qin J-T, Song Z-Y, Cai H-H, Du J-F, Sun S-F, Liu Y; (2016) Photosensitive antibacterial and cytotoxicity performances of a TiO2/carboxymethyl chitosan/poly(vinyl alcohol) nanocomposite hydrogel by in situ radiation construction. Journal of Applied Polymer Science 133(44), 44150. DOI:10.1002/app.44150
  • [7] Czechowska-Biskup R, Wach RA, Stojek P, Kaminska M, Rosiak JM, Ulanski P; (2016) Synthesis of chitosan and carboxymethyl chitosan hydrogels by electron beam irradiation. Progress on Chemistry and Application of Chitin and its Derivatives XXI, 27–45. DOI:10.15259/PCACD.21.03
  • [8] Zhao L, Mitomo H, Nagasawa N, Yoshii F, Kume T; (2003) Radiation synthesis and characteristic of the hydrogels based on carboxymethylated chitin derivatives. Carbohydrate Polymers 51(2), 169–175. DOI:10.1016/S0144-8617(02)00210-2
  • [9] Fan L, Yi J, Tong J, Zhou X, Ge H, Zou S, Wen H, Nie M; (2016) Preparation and characterization of oxidized konjac glucomannan/carboxymethyl chitosan/graphene oxide hydrogel. International Journal of Biological Macromolecules 91, 358–367. DOI:10.1016/j.ijbiomac.2016.05.042
  • [10] Agarwal T, Narayan R, Maji S, Behera S, Kulanthaivel S, Maiti TK, Banerjee I, Pal K, Giri S; (2016) Gelatin/carboxymethyl chitosan based scaffolds for dermal tissue engineering applications. International Journal of Biological Macromolecules 93, 1499–1506. DOI:10.1016/j.ijbiomac.2016.04.028
  • [11] Wahid F, Yin J-J, Xue D-D, Xue H, Lu Y-S, Zhong C, Chu L-Q; (2016) Synthesis and characterization of antibacterial carboxymethyl chitosan/ZnO nanocomposite hydrogels. International Journal of Biological Macromolecules 88, 273–279. DOI:10.1016/j.ijbiomac.2016.03.044
  • [12] Mourya VK, Inamdar NN, Tiwari A; (2010) Carboxymethyl chitosan and its applications. Advanced Materials Letters 1(2), 11–33. DOI:10.5185/amlett.2010.3108
  • [13] Chen L, Du Y, Tian Z, Sun L; (2005) Effect of the degree of deacetylation and the substitution of carboxymethyl chitosan on its aggregation behavior. Journal of Polymer Science Part B: Polymer Physics 43(3), 296–305. DOI:10.1002/polb.20212
  • [14] Zhang L, Guo J, Zhou J, Yang G, Du Y; (2000) Blend membranes from carboxymethylated chitosan/alginate in aqueous solution. Journal of Applied Polymer Science 77(3), 610–616. DOI:10.1002/(SICI)1097-4628(20000718)77:3<610::AID-APP16>3.0.CO;2-B
  • [15] Liu Z, Jiao Y, Zhang Z; (2007) Calcium-carboxymethyl chitosan hydrogel beads for protein drug delivery system. Journal of Applied Polymer Science 103(5), 3164–3168. DOI:10.1002/app.24867
  • [16] ISO 10993-12. Biological evaluation of medical devices – Part 12: Sample preparation and reference material.
  • [17] ISO 10993-5. Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicity.
  • [18] Kozicki M, Kujawa P, Rosiak JM; (2002) Pulse radiolysis study of diacrylate macromonomer in aqueous solution. Radiation Physics and Chemistry 65(2), 133–139. DOI:10.1016/S0969-806X(02)00209-8
  • [19] Varghese S, Elisseeff JH; (2006) Hydrogels for musculoskeletal tissue engineering. In: Werner, C. (ed.) Polymers for regenerative medicine. pp. 95–144. Springer Berlin Heidelberg.
  • [20] Yan H, Dai J, Yang Z, Yang H, Cheng R; (2011) Enhanced and selective adsorption of copper(II) ions on surface carboxymethylated chitosan hydrogel beads. Chemical Engineering Journal 174(2–3), 586–594. DOI:10.1016/j.cej.2011.09.064
  • [21] Muzzarelli RAA; (2009) Genipin-crosslinked chitosan hydrogels as biomedical and pharmaceutical aids. Carbohydrate Polymers 77(1), 1–9. DOI:10.1016/j.carbpol.2009.01.016
  • [22] Czechowska-Biskup R, Rokita B, Ulanski P, Rosiak JM; (2005) Radiation-induced and sonochemical degradation of chitosan as a way to increase its fat-binding capacity. Nuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms 236(1–4), 383–390. DOI:10.1016/j.nimb.2005.04.002

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bwmeta1.element.psjd-fd9754be-4e78-49c7-86eb-ed6dfda87a48
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