Preparation and antibacterial properties of O-carboxymethyl chitosan/lincomycin hydrogels

References

• Zhang F, Li J, Zhu T, et al. Potential of biocompatible regenerated silk fibroin/sodium N-lauroyl sarcosinate hydrogels. J. Biomater. Sci. Polym. Ed. 2015;26:780–795.10.1080/09205063.2015.1058576
   PubMed Web of Science ®Google Scholar
• Cui L, Jia J, Guo Y, et al. Preparation and characterization of IPN hydrogels composed of chitosan and gelatin cross-linked by genipin. Carbohydr. Polym. 2014;99:31–38.10.1016/j.carbpol.2013.08.048
   PubMed Web of Science ®Google Scholar
• Samanta HS, Ray SK. Controlled release of tinidazole and theophylline from chitosan based composite hydrogels. Carbohydr. Polym. 2014;106:109–120.10.1016/j.carbpol.2014.01.097
   PubMed Web of Science ®Google Scholar
• Valderruten NE, Valverde JD, Zuluaga F, et al. Synthesis and characterization of chitosan hydrogels cross-linked with dicarboxylic acids. React. Funct. Poly. 2014;84:21–28.10.1016/j.reactfunctpolym.2014.08.006
   Web of Science ®Google Scholar
• Lee C, Choi JS, Kim I, et al. Decanoic acid-modified glycol chitosan hydrogels containing tightly adsorbed palmityl-acylated exendin-4 as a long-acting sustained-release anti-diabetic system. Acta Biomater. 2014;10:812–820.10.1016/j.actbio.2013.10.009
   PubMed Web of Science ®Google Scholar
• John AH, Rui C, Theun VV, et al. Hydrogels for tissue engineering and regenerative. J. Mater. Chem. B. 2014;2:5319–5338.
   Web of Science ®Google Scholar
• Singh AN, Singh S, Suthar N, et al. Glutaraldehyde-activated chitosan matrix for immobilization of a novel cysteine protease, procerain B. J. Agric. Food Chem. 2011;59:6256–6262.10.1021/jf200472x
   PubMed Web of Science ®Google Scholar
• Lai J. Biocompatibility of genipin and glutaraldehyde cross-linked chitosan materials in the anterior chamber of the eye. Int. J. Mol. Sci. 2012;13:10970–10985.10.3390/ijms130910970
   PubMed Web of Science ®Google Scholar
• Elbarbary AM, Mostafa TB. Effect of γ-rays on carboxymethyl chitosan for use as antioxidant and preservative coating for peach fruit. Carbohydr. Polym. 2014;104:109–117.10.1016/j.carbpol.2014.01.021
   PubMed Web of Science ®Google Scholar
• Anitha A, Divya Rani VV, Krishna R, et al. Synthesis, characterization, cytotoxicity and antibacterial studies of chitosan, O-carboxymethyl and N,O-carboxymethyl chitosan nanoparticles. Carbohydr. Polym. 2009;78:672–677.10.1016/j.carbpol.2009.05.028
   Web of Science ®Google Scholar
• Upadhyaya L, Singh J, Agarwal V, et al. The implications of recent advances in carboxymethyl chitosan based targeted drug delivery and tissue engineering applications. J. Controlled Release. 2014;186:54–87.10.1016/j.jconrel.2014.04.043
   PubMed Web of Science ®Google Scholar
• Hong YJ, Kim JC. Complexation-triggerable liposome mixed with silk protein and chitosan. J. Biomater. Sci. Polym. Ed. 2015;26:766–779.10.1080/09205063.2015.1058574
   PubMed Web of Science ®Google Scholar
• Liu T, Lin Y. Novel pH-sensitive chitosan-based hydrogel for encapsulating poorly water-soluble drugs. Acta Biomater. 2010;6:1423–1429.10.1016/j.actbio.2009.10.010
   PubMed Web of Science ®Google Scholar
• Wu F, Meng G, He J, et al. Antibiotic-loaded chitosan hydrogel with superior dual functions: antibacterial efficacy and osteoblastic cell responses. ACS Appl. Mater. Interfaces. 2014;6:10005–10013.
   PubMed Web of Science ®Google Scholar
• Clasen C, Wilhelms T, Kulicke WM. Formation and characterization of chitosan membranes. Biomacromolecules. 2006;7:3210–3222.10.1021/bm060486x
   PubMed Web of Science ®Google Scholar
• Cojocariu A, Profire L, Aflori M, et al. In vitro drug release from chitosan/Cloisite 15A hydrogels. Appl. Clay Sci. 2012;57:1–9.10.1016/j.clay.2011.11.030
   Web of Science ®Google Scholar
• Wang Y, Chai Z, Wang N, et al. Preparation and responsive behaviors of chitosan-functionalized nanoparticles via a boronic acid-related reaction. J. Biomater. Sci. Polym. Ed. 2015;26:617–628.10.1080/09205063.2015.1053169
   PubMed Web of Science ®Google Scholar
• Chen J, Sun J, Yang L, et al. Preparation and characterization of a novel IPN hydrogel memberane of poly(N-isopropylacrylamide)/carboxymethyl chitosan (PNIPAAM/CMCS). Radiat. Phys. Chem. 2007;76:1425–1429.10.1016/j.radphyschem.2007.02.045
   Web of Science ®Google Scholar
• Kusuma HS, Al-sa’bani AF, Darmokoesoemo H. N,O-carboxymethyl chitosan: an innovation in new natural preservative from shrimp shell waste with a nutritional value and health orientation. Procedia Food Sci. 2015;3:35–51.10.1016/j.profoo.2015.01.004
   Google Scholar
• Li X, Kong X, Zhang Z, et al. Cytotoxicity and biocompatibility evaluation of N,O-carboxymethyl chitosan/oxidized alginate hydrogel for drug delivery application. Int. J. Biol. Macromol. 2012;50:1299–1305.10.1016/j.ijbiomac.2012.03.008
   PubMed Web of Science ®Google Scholar
• Tavakol M, Vasheghani-Farahani E, Dolatabadi-Farahani T, et al. Sulfasalazine release from alginate-N,O-carboxymethyl chitosan gel beads coated by chitosan. Carbohydr. Polym. 2009;77:326–330.10.1016/j.carbpol.2009.01.005
   Web of Science ®Google Scholar
• Li X, Chen S, Zhang B, et al. In situ injectable nano-composite hydrogel composed of curcumin, N,O-carboxymethyl chitosan and oxidized alginate for wound healing application. Int. J. Pharm. 2012;437:110–119.10.1016/j.ijpharm.2012.08.001
   PubMed Web of Science ®Google Scholar
• Huang X, Zhang Y, Zhang X, et al. Influence of radiation crosslinked carboxymethyl-chitosan/gelatin hydrogel on cutaneous wound healing. Mater. Sci. Eng. C. 2013;33:4816–4824.10.1016/j.msec.2013.07.044
   PubMed Web of Science ®Google Scholar
• Luo Y, Teng Z, Wang X, et al. Development of carboxymethyl chitosan hydrogel beads in alcohol-aqueous binary solvent for nutrient delivery applications. Food Hydrocolloids. 2013;31:332–339.10.1016/j.foodhyd.2012.11.011
   Web of Science ®Google Scholar
• Chen R, Wang G, Chen C, et al. Development of N,O-(carboxymethyl) chitosan/collagen matrixes as a wound dressing. Biomacromolecules. 2006;7:1058–1064.10.1021/bm050754b
   PubMed Web of Science ®Google Scholar
• Wang J, Chen J, Zong J, et al. Calcium carbonate/carboxymethyl chitosan hybrid microspheres and nanospheres for drug delivery. J. Phys. Chem. C. 2010;114:18940–18945.10.1021/jp105906p
   Web of Science ®Google Scholar
• Laudenslager MJ, Schiffman JD, Schauer CL. Carboxymethyl chitosan as a matrix material for platinum, gold, and silver nanoparticles. Biomacromolecules. 2008;9:2682–2685.10.1021/bm800835e
   PubMed Web of Science ®Google Scholar
• Zhou Y, Zhao Y, Wang L, et al. Radiation synthesis and characterization of nanosilver/gelatin/carboxymethyl chitosan hydrogel. Radiat. Phys. Chem. 2012;81:553–560.10.1016/j.radphyschem.2012.01.014
   Web of Science ®Google Scholar
• Yin L, Fei L, Cui F, et al. Superporous hydrogels containing poly(acrylic acid-co-acrylamide)/O-carboxymethyl chitosan interpenetrating polymer networks. Biomaterials. 2007;28:1258–1266.10.1016/j.biomaterials.2006.11.008
   PubMed Web of Science ®Google Scholar
• Gujarathi NA, Rane BR, Patel JK. pH sensitive polyelectrolyte complex of O-carboxymethyl chitosan and poly (acrylic acid) cross-linked with calcium for sustained delivery of acid susceptible drugs. Int. J. Pharm. 2012;436:418–425.10.1016/j.ijpharm.2012.07.016
   PubMed Web of Science ®Google Scholar
• Wang J, Gao X, Wang J, et al. O-(carboxymethyl)-chitosan nanofiltration membrane surface functionalized with graphene oxide nanosheets for enhanced desalting properties. ACS Appl. Mater. Interfaces. 2015;7:4381–4389.10.1021/am508903g
   PubMed Web of Science ®Google Scholar
• Vaghani SS, Patel MM, Satish CS. Synthesis and characterization of pH-sensitive hydrogel composed of carboxymethyl chitosan for colon targeted delivery of ornidazole. Carbohydr. Res. 2012;347:76–82.10.1016/j.carres.2011.04.048
   PubMed Web of Science ®Google Scholar
• Qian G, Wu Y, Yang X, et al. Exploiting polymorphism in the purity enhancement of lincomycin hydrochloride. Chem. Eng. Sci. 2012;77:42–46.10.1016/j.ces.2012.02.004
   Web of Science ®Google Scholar
• Andreozzi R, Canterino M, Giudice RL, et al. Lincomycin solar photodegradation, algal toxicity and removal from wastewaters by means of ozonation. Water Res. 2006;40:630–638.10.1016/j.watres.2005.11.023
   PubMed Web of Science ®Google Scholar
• Vučićević-Prčetić K, Cservenák R, Radulović N. Development and validation of liquid chromatography tandem mass spectrometry methods for the determination of gentamicin, lincomycin, and spectinomycin in the presence of their impurities in pharmaceutical formulations. J. Pharm. Biomed. Anal. 2011;56:736–742.10.1016/j.jpba.2011.07.031
   PubMed Web of Science ®Google Scholar
• Skoufos J, Mavrogianni VS, Tzora A, et al. Use of lincomycin to control respiratory infections in lambs: effects on health and production. Small Ruminant Res. 2006;66:214–221.10.1016/j.smallrumres.2005.09.006
   Web of Science ®Google Scholar
• Čermák L, Kopecký J, Novotná J, et al. Bacterial communities of two contrasting soils reacted differently to lincomycin treatment. Appl. Soil Ecol. 2008;40:348–358.10.1016/j.apsoil.2008.06.001
   Web of Science ®Google Scholar
• Arimitsu H, Tsukamoto K, Ochi S, et al. Lincomycin-induced over-expression of mature recombinant cholera toxin B subunit and the holotoxin in Escherichia coli. Protein Expr. Purif. 2009;67:96–103.10.1016/j.pep.2009.04.011
   PubMed Web of Science ®Google Scholar
• Noomrio MH, Zhang R, Eisenthal R, et al. Characterisation of hydrogel gel swelling by molecular exclusion. Biotechnol. Lett. 2005;27:1587–1590.10.1007/s10529-005-1801-2
   PubMed Web of Science ®Google Scholar
• He DB, Shi XM, Shi Y, et al. Gelation and swelling behavior of oxidized konjac glucomannan/chitosan hydrogel. J. Wuhan. Univ. Nat. Sci. 2002;7:481–485.
   Google Scholar
• Spinks GM, Lee CK, Wallace GG, et al. Swelling behavior of chitosan hydrogels in ionic liquid−water binary systems. Langmuir. 2006;22:9375–9379.10.1021/la061586r
   PubMed Web of Science ®Google Scholar
• Fang W, Ma L, Zheng J, et al. Fabrication of silver-loaded hollow mesoporous aluminosilica nanoparticles and their antibacterial activity. J. Mater. Sci. 2014;49:3407–3413.10.1007/s10853-014-8050-5
   Web of Science ®Google Scholar
• Babić MM, Antić KM, Vuković JSJ, et al. Oxaprozin/poly(2-hydroxyethyl acrylate/itaconic acid) hydrogels: morphological, thermal, swelling, drug release and antibacterial properties. J. Mater. Sci. 2015;50:906–922.10.1007/s10853-014-8651-z
   Web of Science ®Google Scholar
• Jung J, Zhao Y. Impact of the structural differences between α- and β-chitosan on their depolymerizing reaction and antibacterial activity. J. Agric. Food Chem. 2013;61:8783–8789.10.1021/jf4018965
   PubMed Web of Science ®Google Scholar
• Upadhyaya L, Singh J, Agarwal V, et al. Efficient water soluble nanostructured ZnO grafted O-carboxymethyl chitosan/curcumin-nanocomposite for cancer therapy. Process Biochem. 2015;50:678–688.10.1016/j.procbio.2014.12.029
   Web of Science ®Google Scholar