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Carboxymethyl chitosan: Properties and biomedical applications

Shariatinia, Zahra·2018·International Journal of Biological Macromolecules
DOI 10.1016/j.ijbiomac.2018.09.131
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Abstract

Chitosan (CS) derivatives are widely used in various biomedical applications due to their unique properties like biocompatibility, mucoadhesion, non-toxicity and capability to form gels. Furthermore, they are suitable candidates to manufacture films, tablets and nanotechnology-based systems which have the possibility for commercial production as well as industrial scale-up. CS has a low solubility at physiological pH (>6.0), thus limiting its application in systems needing higher solubility and drug release rate. Another drawback of CS is its fast water adsorption and high swelling degree in aqueous media, which can cause rapid drug release. Chemical modification of two hydroxyl and one amino groups existing on the CS chains using the carboxymethyl moieties will alter the CS properties. The water solubility of carboxymethyl chitosan (CMC) at various pH environments is governed by the carboxymethylation degree. The CMC derivatives can interact with cells which successfully result in cell growth/tissue regeneration and wound healing. They are also employed in the cosmetics production because of their moisture absorption-retention, antimicrobial and emulsion stabilizing characteristics. This work will highlight the most recent applications of CMC derivatives with antimicrobial, anticancer, antitumor, antioxidant and antifungal biological activities in various areas like wound healing, tissue engineering, drug/enzyme delivery, bioimaging and cosmetics.

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Research works printed but not linked: 180

  1. Ling, 2015, Multifunctional cellulosic paper based on quaternized chitosan and gold nanoparticle-reduced graphene oxide via electrostatic self-assembly, J. Mater. Chem. A, 3, 7422, 10.1039/C4TA07160C · DOI
  2. Fazli, 2017, Controlled release of cefazolin sodium antibiotic drug from electrospun chitosan-polyethylene oxide nanofibrous mats, Mater. Sci. Eng. C, 71, 641, 10.1016/j.msec.2016.10.048 · DOI
  3. Fazli, 2016, A novel chitosan-polyethylene oxide nanofibrous mat designed for controlled co-release of hydrocortisone and imipenem/cilastatin drugs, Int. J. Pharm., 513, 636, 10.1016/j.ijpharm.2016.09.078 · DOI
  4. Shariatinia, 2018, Chapter 4. Advances in polymers for drug delivery and wound healing applications
  5. Shariatinia, 2018, Synthesis of zeolite NaY and its nanocomposites with chitosan as adsorbents for lead(II) removal from aqueous solution, Powder Technol., 338, 744, 10.1016/j.powtec.2018.07.082 · DOI
  6. Shariatinia, 2018, Chitosan-based hydrogels: preparation, properties and applications, Int. J. Biol. Macromol., 115, 194, 10.1016/j.ijbiomac.2018.04.034 · DOI
  7. Samadi, 2016, Synthesis of raloxifene–chitosan conjugate: a novel chitosan derivative as a potential targeting vehicle, Int. J. Biol. Macromol., 82, 599, 10.1016/j.ijbiomac.2015.10.041 · DOI
  8. Garaiova, 2012, A., Bjørkøy, L. Davies Cde, cellular uptake of DNA–chitosan nanoparticles: the role of clathrin- and caveolae-mediated pathways, Int. J. Biol. Macromol., 51, 1043, 10.1016/j.ijbiomac.2012.08.016 · DOI
  9. El-Sherbiny, 2016, New trimethyl chitosan-based composite nanoparticles as promising antibacterial agents, Drug Dev. Ind. Pharm., 42, 720, 10.3109/03639045.2015.1075035 · DOI
  10. He, 2013, Trimethyl chitosan-cysteine nanoparticles for systemic delivery of TNF-α siRNA via oral and intraperitoneal routes, Pharm. Res., 30, 2596, 10.1007/s11095-013-1086-4 · DOI
  11. Hu, 2014, Folate conjugated trimethyl chitosan/graphene oxide nanocomplexes as potential carriers for drug and gene delivery, Mater. Lett., 125, 82, 10.1016/j.matlet.2014.03.133 · DOI
  12. Anitha, 2011, Efficient water soluble O-carboxymethyl chitosan nanocarrier for the delivery of curcumin to cancer cells, Carbohydr. Polym., 83, 452, 10.1016/j.carbpol.2010.08.008 · DOI
  13. Rahmani, 2016, Methylated 4-N,N dimethyl aminobenzyl N,O carboxymethyl chitosanas a new chitosan derivative: synthesis, characterization, cytotoxicity and antibacterial activity, Carbohydr. Polym., 149, 131, 10.1016/j.carbpol.2016.04.116 · DOI
  14. Geisberger, 2013, Trimethyl and carboxymethyl chitosan carriers for bio-active polymer–inorganic nanocomposites, Carbohydr. Polym., 91, 58, 10.1016/j.carbpol.2012.08.009 · DOI
  15. Patrulea, 2015, Optimized synthesis of O-carboxymethyl-N,N,N-trimethyl chitosan, Carbohydr. Polym., 122, 46, 10.1016/j.carbpol.2014.12.014 · DOI
  16. Xu, 2010, Synthesis, characteristic and antibacterial activity of N,N,N-trimethyl chitosan and its carboxymethyl derivatives, Carbohydr. Polym., 81, 931, 10.1016/j.carbpol.2010.04.008 · DOI
  17. Zhang, 2014, Cytocompatible injectable carboxymethyl chitosan/N-isopropylacrylamide hydrogels for localized drug delivery, Carbohydr. Polym., 103, 110, 10.1016/j.carbpol.2013.12.017 · DOI
  18. Bai, 2017, Systematic investigation of fabrication conditions of nanocarrier based on carboxymethyl chitosan for sustained release of insulin, Int. J. Biol. Macromol., 102, 468, 10.1016/j.ijbiomac.2017.03.181 · DOI
  19. Paradossi, 1992, Branched-chain analogues of linear polysaccharides: a spectroscopic and conformational investigation of chitosan derivatives, Int. J. Biol. Macromol., 14, 73, 10.1016/0141-8130(92)90002-P · DOI
  20. Heuser, 2009, Chitosan–copper paint types as antifouling, J. Chil. Chem. Soc., 54, 448, 10.4067/S0717-97072009000400028 · DOI
  21. Vo, 2017, Silver deposited carboxymethyl chitosan-grafted magnetic nanoparticles as dual action deliverable antimicrobial materials, Mater. Sci. Eng. C, 73, 544, 10.1016/j.msec.2016.12.066 · DOI
  22. Berdy, 2012, Thoughts and facts about antibiotics: where we are now and where we are heading, J. Antibiot., 65, 385, 10.1038/ja.2012.27 · DOI
  23. Song, 2008, What's new on the antimicrobial horizon?, Int. J. Antimicrob. Agents, 32, S207, 10.1016/S0924-8579(09)70004-4 · DOI
  24. Fan, 2014, A novel wound dressing based on Ag/graphene polymer hydrogel: effectively kill bacteria and accelerate wound healing, Adv. Funct. Mater., 24, 3933, 10.1002/adfm.201304202 · DOI
  25. Du, 2015, Supramolecular hydrogelators and hydrogels: from soft matter to molecular biomaterials, Chem. Rev., 115, 13165, 10.1021/acs.chemrev.5b00299 · DOI
  26. Kojic, 2012, Focal infection treatment using laser-mediated heating of injectable silk hydrogels with gold nanoparticles, Adv. Funct. Mater., 22, 3793, 10.1002/adfm.201200382 · DOI
  27. Laverty, 2014, Ultrashort cationic naphthalene-derived self-assembled peptides as antimicrobial nanomaterials, Biomacromolecules, 15, 3429, 10.1021/bm500981y · DOI
  28. Ng, 2014, Antimicrobial hydrogels: a new weapon in the arsenal against multidrug-resistant infections, Adv. Drug Deliv. Rev., 78, 46, 10.1016/j.addr.2014.10.028 · DOI
  29. Barnard, 2011, Degradable self-assembling dendrons for gene delivery: experimental and theoretical insights into the barriers to cellular uptake, J. Am. Chem. Soc., 133, 20288, 10.1021/ja2070736 · DOI
  30. Chen, 2015, Charge-conversional and reduction-sensitive poly(vinyl alcohol) nanogels for enhanced cell uptake and efficient intracellular doxorubicin release, J. Control. Release, 205, 15, 10.1016/j.jconrel.2014.11.012 · DOI
  31. Bieser, 2008, Supramolecular self-organization of potential hydrogelators on attracting surfaces, Supramol. Chem., 20, 363, 10.1080/10610270701260325 · DOI
  32. Jayawarna, 2006, Nanostructured hydrogels for three-dimensional cell culture through self-assembly of fluorenylmethoxycarbonyl-dipeptides, Adv. Mater., 18, 611, 10.1002/adma.200501522 · DOI
  33. Babu, 2012, Self-assembled gelators for organic electronics, Angew. Chem. Int. Ed., 51, 1766, 10.1002/anie.201106767 · DOI
  34. Upadhyaya, 2015, Efficient water soluble nanostructured ZnO grafted O-carboxymethyl chitosan/curcumin nanocomposite for cancer therapy, Process Biochem., 50, 678, 10.1016/j.procbio.2014.12.029 · DOI
  35. Chen, 2004, A novel pH-sensitive hydrogel composed of N,O-carboxymethyl chitosan and alginate cross-linked by genipin for protein drug delivery, J. Control. Release, 96, 285, 10.1016/j.jconrel.2004.02.002 · DOI
  36. Liu, 2001, Antibacterial action of chitosan and carboxymethylated chitosan, J. Appl. Polym. Sci., 79, 1324, 10.1002/1097-4628(20010214)79:7<1324::AID-APP210>3.0.CO;2-L · DOI
  37. Varma, 2004, Metal complexation by chitosan and its derivatives: a review, Carbohydr. Polym., 55, 77, 10.1016/j.carbpol.2003.08.005 · DOI
  38. Ngah, 1999, Adsorption of gold(III) ions onto chitosan and Ncarboxymethyl chitosan: equilibrium studies, Ind. Eng. Chem. Res., 38, 1411, 10.1021/ie9803164 · DOI
  39. Guibal, 2004, Interactions of metal ions with chitosan-based sorbents: a review, Sep. Purif. Technol., 38, 43, 10.1016/j.seppur.2003.10.004 · DOI
  40. Guo, 2014, Synthetic biodegradable functional polymers for tissue engineering: a brief review, Sci China Chem, 57, 490, 10.1007/s11426-014-5086-y · DOI · Paper page
  41. Horner, 2000, Regenerating the damaged central nervous system, Nature, 407, 963, 10.1038/35039559 · DOI
  42. Leor, 2000, Bioengineered cardiac grafts a new approach to repair the infarcted myocardium?, Circulation, 102, 10.1161/circ.102.suppl_3.III-56 · DOI
  43. Hutmacher, 2000, Scaffolds in tissue engineering bone and cartilage, Biomaterials, 21, 2529, 10.1016/S0142-9612(00)00121-6 · DOI
  44. Hollister, 2005, Porous scaffold design for tissue engineering, Nat. Mater., 4, 518, 10.1038/nmat1421 · DOI
  45. Ma, 2014, Nanofibrous electroactive scaffolds from a chitosan-grafted-aniline tetramer by electrospinning for tissue engineering, RSC Adv., 4, 13652, 10.1039/c4ra00083h · DOI
  46. Li, 2014, Electroactive nanofibrous biomimetic scaffolds by thermally induced phase separation, J. Mater. Chem. B, 2, 6119, 10.1039/C4TB00493K · DOI
  47. Guo, 2012, Electroactive porous tubular scaffolds with degradability and non-cytotoxicity for neural tissue regeneration, Acta Biomater., 8, 144, 10.1016/j.actbio.2011.09.027 · DOI
  48. Naahidi, 2017, Biocompatibility of hydrogel-based scaffolds for tissue engineering applications, Biotechnol. Adv., 35, 530, 10.1016/j.biotechadv.2017.05.006 · DOI
  49. Slaughter, 2009, Hydrogels in regenerative medicine, Adv. Mater., 21, 3307, 10.1002/adma.200802106 · DOI · Paper page
  50. Jaikumar, 2015, Injectable alginate-O-carboxymethyl chitosan/nano fibrin composite hydrogels for adipose tissue engineering, Int. J. Biol. Macromol., 74, 318, 10.1016/j.ijbiomac.2014.12.037 · DOI
  51. Diamond, 2001, Clinical implications of postsurgical adhesions, Hum. Reprod. Update, 7, 567, 10.1093/humupd/7.6.567 · DOI
  52. Broek, 2013, Adhesiolysis-related morbidity in abdominal surgery, Ann. Surg., 258, 98, 10.1097/SLA.0b013e31826f4969 · DOI
  53. Costain, 1997, Prevention of postsurgical adhesions with N,O-carboxymethyl chitosan: examination of the most efficacious preparation and the effect of N,O-carboxymethyl chitosan on postsurgical healing, Surgery, 121, 314, 10.1016/S0039-6060(97)90360-3 · DOI
  54. Venkatrajah, 2013, Synthesis of carboxymethyl chitosan and coating on wound dressing gauze for wound healing, Pak. J. Biol. Sci., 16, 1438, 10.3923/pjbs.2013.1438.1448 · DOI
  55. Chen, 2006, Development of N,O-(carboxymethyl)chitosan/collagen matrixes as a wound dressing, Biomacromolecules, 7, 1058, 10.1021/bm050754b · DOI
  56. Fonseca-Santos, 2017, An overview of carboxymethyl derivatives of chitosan: their use as biomaterials and drug delivery systems, Mater. Sci. Eng. C, 77, 1349, 10.1016/j.msec.2017.03.198 · DOI
  57. Kong, 2010, Antimicrobial properties of chitosan and mode of action: a state of the art review, Int. J. Food Microbiol., 144, 51, 10.1016/j.ijfoodmicro.2010.09.012 · DOI · Paper page
  58. Seyfarth, 2008, Antifungal effect of high- and low-molecular-weight chitosan hydrochloride, carboxymethyl chitosan, chitosan oligosaccharide and N-acetyl-d-glucosamine against Candida albicans, Candida krusei and Candida glabrata, Int. J. Pharm., 353, 139
  59. Jayakumar, 2010, Novel carboxymethyl derivatives of chitin and chitosan materials and their biomedical applications, Prog. Mater. Sci., 55, 675, 10.1016/j.pmatsci.2010.03.001 · DOI
  60. Tantala, 2012, Antimicrobial activity of chitosan and carboxymethyl chitosan from different types and sources of chitosan, Ital. J. Food Sci., 24, 97
  61. Loke, 2000, Wound dressing with sustained anti-microbial capability, J. Biomed. Mater. Res., 53, 8, 10.1002/(SICI)1097-4636(2000)53:1<8::AID-JBM2>3.0.CO;2-3 · DOI
  62. Pillai, 2001, Polymers in drug delivery, Curr. Opin. Chem. Biol., 5, 447, 10.1016/S1367-5931(00)00227-1 · DOI
  63. Upadhyaya, 2014, The implications of recent advances in carboxymethyl chitosan based targeted drug delivery and tissue engineering applications, J. Control. Release, 186, 54, 10.1016/j.jconrel.2014.04.043 · DOI
  64. Mourya, 2010, Carboxymethyl chitosan and its applications, Adv. Mater. Lett., 1, 11, 10.5185/amlett.2010.3108 · DOI
  65. Jimtaisong, 2014, Utilization of carboxymethyl chitosan in cosmetics, Int. J. Cosmet. Sci., 36, 12, 10.1111/ics.12102 · DOI
  66. Dutta, 2004, Chitin and chitosan: chemistry, properties and applications, J. Sci. Ind. Res., 63, 20
  67. Muzzarelli, 1988, Carboxymethylated chitins and chitosans, Carbohydr. Polym., 8, 1, 10.1016/0144-8617(88)90032-X · DOI
  68. Muzzarelli, 2002, N-Carboxymethyl chitosan in innovative cosmeceutical products, J. Appl. Cosmetol., 20, 201
  69. Feng, 2015, Surface charge effect on mucoadhesion of chitosan based nanogels for local anti-colorectal cancer drug delivery, Colloids Surf. B: Biointerfaces, 128, 439, 10.1016/j.colsurfb.2015.02.042 · DOI
  70. Sun, 2006, Preparation, characterization and antimicrobial activity of quaternized carboxymethyl chitosan and application as pulp-cap, Polymer, 47, 1796, 10.1016/j.polymer.2006.01.073 · DOI
  71. Anitha, 2009, Synthesis, characterization, cytotoxicity and antibacterial studies of chitosan, O-carboxymethyl and N,O-carboxymethyl chitosan nanoparticles, Carbohydr. Polym., 78, 672, 10.1016/j.carbpol.2009.05.028 · DOI
  72. Liu, 2012, Study on antibacterial activity of O-carboxymethyl chitosan sodium salt and spinnability of O-carboxymethyl chitosan sodium salt/cellulose polyblends in N-methylmorpholine-N-oxide system, Carbohydr. Polym., 104, 10.1016/j.carbpol.2012.02.057 · DOI
  73. Abou-Okeil, 2012, Ag nanoparticles growing onto cotton fabric using chitosan as a template, J. Nat. Fiber., 9, 61, 10.1080/15440478.2011.651841 · DOI
  74. Abou-Okeil, 2012, Investigation of silver nanoparticles synthesis using aminated-beta-cyclodextrin, Carbohydr. Polym., 89, 1, 10.1016/j.carbpol.2012.01.038 · DOI
  75. Fouda, 2013, Antimicrobial activity of carboxymethyl chitosan/polyethylene oxide nanofibers embedded silver nanoparticles, Carbohydr. Polym., 92, 1012, 10.1016/j.carbpol.2012.10.047 · DOI
  76. Huang, 2015, Carboxymethyl chitosan/clay nanocomposites and their coppercomplexes: fabrication and property, Carbohydr. Polym., 134, 390, 10.1016/j.carbpol.2015.07.089 · DOI
  77. Anwar, 1990, Testing the susceptibility of bacterial in biofilms to antibacterial agents, Antimicrob. Agents Chemother., 34, 2043, 10.1128/AAC.34.11.2043 · DOI
  78. Khoury, 1992, Prevention and control of bacterial infections associated with medical devices, ASAIO J., 38, M174, 10.1097/00002480-199207000-00013 · DOI
  79. Chen, 2012, Carboxymethyl chitosan-functionalized magnetic nanoparticles for disruption of biofilms of Staphylococcus aureus and Escherichia coli, Ind. Eng. Chem. Res., 51, 13164, 10.1021/ie301522w · DOI
  80. Wahid, 2017, Facile fabrication of moldable antibacterial carboxymethyl chitosan supramolecular hydrogels cross-linked by metal ions complexation, Carbohydr. Polym., 165, 455, 10.1016/j.carbpol.2017.02.085 · DOI
  81. Dong, 2010, Pharmacokinetics and biodegradation mechanisms of a versatile carboxymethyl derivative of chitosan in rats: in vivo and in vitro evaluation, Biomacromolecules, 11, 1527, 10.1021/bm100158p · DOI
  82. Ling, 2013, Novel antibacterial paper based on quaternized carboxymethyl chitosan/organic montmorillonite/Ag NP nanocomposites, Ind. Crop. Prod., 51, 470, 10.1016/j.indcrop.2013.09.040 · DOI
  83. Wahid, 2017, Preparation, characterization and antibacterial applications of carboxymethyl chitosan/CuO nanocomposite hydrogels, Int. J. Biol. Macromol., 101, 690, 10.1016/j.ijbiomac.2017.03.132 · DOI
  84. Wahid, 2016, Synthesis and characterization of antibacterial carboxymethyl chitosan/ZnO nanocomposite hydrogels, Int. J. Biol. Macromol., 88, 273, 10.1016/j.ijbiomac.2016.03.044 · DOI
  85. Mohamed, 2014, Synthesis and characterization of some novel antimicrobial thiosemicarbazone O-carboxymethyl chitosan derivatives, Int. J. Biol. Macromol., 63, 163, 10.1016/j.ijbiomac.2013.10.044 · DOI
  86. Wu, 2014, Antibiotic-loaded chitosan hydrogel with superior dual functions: antibacterial efficacy and osteoblastic cell responses, ACS Appl. Mater. Interfaces, 6, 10005, 10.1021/am502537k · DOI
  87. Yang, 2014, Flocculation of Escherichia coli using a quaternary ammonium salt grafted carboxymethyl chitosan flocculant, Environ. Sci. Technol., 48, 6867, 10.1021/es500415v · DOI
  88. El Shafei, 2011, ZnO/carboxymethyl chitosan bionano-composite to impart antibacterial and UV protection for cotton fabric, Carbohydr. Polym., 83, 920, 10.1016/j.carbpol.2010.08.083 · DOI
  89. Zheng, 2011, Synthesis, characterization and bio-logical safety of O-carboxymethyl chitosan used to treat Sarcoma 180 tumor, Carbohydr. Polym., 86, 231, 10.1016/j.carbpol.2011.04.038 · DOI
  90. Jiang, 2015, Preparation and anti-tumor metastasis of carboxymethyl chitosan, Carbohydr. Polym., 125, 53, 10.1016/j.carbpol.2015.02.039 · DOI
  91. Felber, 2012, pH-sensitive vesicles, polymeric micelles, and nanospheres prepared with polycarboxylates, Adv. Drug Deliv. Rev., 64, 979, 10.1016/j.addr.2011.09.006 · DOI
  92. Wang, 2014, Amphiphilic carboxymethyl chitosan-quercetin conjugate with P-gp inhibitory properties for oral delivery of paclitaxel, Biomaterials, 35, 7654, 10.1016/j.biomaterials.2014.05.053 · DOI
  93. Yang, 2016, Carboxymethyl chitosan-mediated synthesis of hyaluronic acid-targeted graphene oxide for cancer drug delivery, Carbohydr. Polym., 135, 72, 10.1016/j.carbpol.2015.08.058 · DOI
  94. Wang, 2017, 3-Carboxyphenylboronic acid-modified carboxymethyl chitosan nanoparticles for improved tumor targeting and inhibitory, Eur. J. Pharm. Biopharm., 113, 168, 10.1016/j.ejpb.2016.12.034 · DOI
  95. Zhang, 2017, Comparison in docetaxel-loaded nanoparticles based on three different carboxymethyl chitosans, Int. J. Biol. Macromol., 101, 1012, 10.1016/j.ijbiomac.2017.03.195 · DOI
  96. Tu, 2017, miRNA-218-loaded carboxymethyl chitosan - tocopherol nanoparticle to suppress the proliferation of gastrointestinal stromal tumor growth, Mater. Sci. Eng. C, 72, 177, 10.1016/j.msec.2016.10.052 · DOI
  97. Jena, 2017, Potential of amphiphilic graft copolymer α-tocopherol succinate-g-carboxymethyl chitosan in modulating the permeability and anticancer efficacy of tamoxifen, Eur. J. Pharm. Sci., 101, 149, 10.1016/j.ejps.2017.02.023 · DOI
  98. Kim, 2017, Preparation and anticancer effect of transferrin-modified pH-sensitive polymeric drug nanoparticle for targeted cancer therapy, J. Ind. Eng. Chem., 54, 298, 10.1016/j.jiec.2017.06.004 · DOI
  99. Jiang, 2017, Preparation and pharmacological evaluation of norcantharidin-conjugated carboxymethyl chitosan in mice bearing hepatocellular carcinoma, Carbohydr. Polym., 174, 282, 10.1016/j.carbpol.2017.06.072 · DOI
  100. Verma, 2016, Targeted smart pH and thermoresponsive N,O-carboxymethyl chitosan conjugated nanogels for enhanced therapeutic efficacy of DOX in MCF-7 breast cancer cells, Bioconjug. Chem., 27, 2605, 10.1021/acs.bioconjchem.6b00366 · DOI
  101. Seifried, 2007, A review of the interaction among dietary antioxidants and reactive oxygen species, J. Nutr. Biochem., 18, 567, 10.1016/j.jnutbio.2006.10.007 · DOI
  102. Valko, 2007, Free radicals and antioxidants in normal physiological functions and human disease, Int. J. Biochem. Cell Biol., 39, 44, 10.1016/j.biocel.2006.07.001 · DOI · Paper page
  103. Liu, 2012, Preparation, antioxidant and antitumor activities in vitro of different derivatives of Levan from endophytic bacterium Paenibacillus polymyxa EJS-3, Food Chem. Toxicol., 50, 767, 10.1016/j.fct.2011.11.016 · DOI
  104. Jin, 2011, Sulfated modification and antioxidant activity of exopolysaccahrides produced by Enterobacter cloacae Z0206, Int. J. Biol. Macromol., 48, 607, 10.1016/j.ijbiomac.2011.01.023 · DOI
  105. Shao, 2013, In intro antioxidant activities of different sulfated polysaccharides from chlorophytan seaweeds Ulva fasciata, Int. J. Biol. Macromol., 59, 295, 10.1016/j.ijbiomac.2013.04.048 · DOI
  106. Zhao, 2011, Biochemical activities of N,O-carboxymethyl chitosan from squid cartilage, Carbohydr. Polym., 85, 832, 10.1016/j.carbpol.2011.04.007 · DOI
  107. Sun, 2007, Preparation of chitosan oligomers and their antioxidant activity, Eur. Food Res. Technol., 225, 451, 10.1007/s00217-006-0439-1 · DOI
  108. Guo, 2005, The synthesis and antioxidant activity of the Schiff bases of chitosan and carboxymethyl chitosan, Bioorg. Med. Chem. Lett., 15, 4600, 10.1016/j.bmcl.2005.06.095 · DOI
  109. Guo, 2008, Synthesis and hydroxyl radicals scavenging activity of quaternized carboxymethyl chitosan, Carbohydr. Polym., 73, 173, 10.1016/j.carbpol.2007.10.021 · DOI
  110. Liu, 2013, Preparation, characterization and antioxidant activity of phenolic acids grafted carboxymethyl chitosan, Int. J. Biol. Macromol., 62, 85, 10.1016/j.ijbiomac.2013.08.040 · DOI
  111. Liu, 2017, Preparation, characterization and antioxidant activity of silk peptides grafted carboxymethyl chitosan, Int. J. Biol. Macromol., 104A, 732, 10.1016/j.ijbiomac.2017.06.071 · DOI
  112. Costa, 2014, Antimicrobial and antibiofilm activity of chitosan on the oral pathogen Candida albicans, Pathogens, 3, 908, 10.3390/pathogens3040908 · DOI
  113. Kulikov, 2014, Antifungal activity of oligochitosans (short chain chitosans) against some Candida species and clinical isolates of Candida albicans: molecular weight-activity relationship, Eur. J. Med. Chem., 74, 169, 10.1016/j.ejmech.2013.12.017 · DOI
  114. Sardi, 2013, Candida species: current epidemiology, pathogenicity, biofilm formation, natural antifungal products and new therapeutic options, J. Med. Microbiol., 62, 10, 10.1099/jmm.0.045054-0 · DOI · Paper page
  115. Verlee, 2017, Recent developments in antibacterial and antifungal chitosan and its derivatives, Carbohydr. Polym., 164, 268, 10.1016/j.carbpol.2017.02.001 · DOI
  116. Kurniasih, 2018, Carboxymethyl chitosan as an antifungal agent on gauze, Int. J. Biol. Macromol., 119, 166, 10.1016/j.ijbiomac.2018.07.038 · DOI
  117. Alburquenque, 2010, Antifungal activity of low molecular weight chitosan against clinical isolates of Candida spp, Med. Mycol., 48, 1018, 10.3109/13693786.2010.486412 · DOI
  118. Tan, 2015, Enhancing the stability and antibiofilm activity of DspB by immobilization on carboxymethyl chitosan nanoparticles, Microbiol. Res., 178, 35, 10.1016/j.micres.2015.06.001 · DOI
  119. Tan, 2011, Carboxymethyl chitosan prevents formation of broad-spectrum biofilm, Carbohydr. Polym., 84, 1365, 10.1016/j.carbpol.2011.01.036 · DOI
  120. Tan, 2016, Antibiofilm activity of carboxymethyl chitosan on the biofilms of non-Candida albicans Candida species, Carbohydr. Polym., 149, 77, 10.1016/j.carbpol.2016.04.101 · DOI
  121. Khan, 2012, Preparation and evaluation of spray dried microparticles using chitosan and novel chitosan derivative for controlled release of an antipsychotic drug, Int. J. Biol. Pharm. Res., 3, 113
  122. Luo, 2012, Development of zinc nanoparticles coated with carboxymethyl chitosan for encapsulation and controlled release of vitamin D3, J. Agric. Food Chem., 60, 836, 10.1021/jf204194z · DOI
  123. Wang, 2010, Carbonate/carboxymethyl chitosan hybrid microspheres and nanospheres for drug delivery, J. Phys. Chem. C, 114, 18940, 10.1021/jp105906p · DOI
  124. Chen, 2004, A novel pH-sensitive hydrogel composed of N,O-carboxymethyl chitosan and alginate cross-linked by genipin for protein drug delivery, J. Control. Release, 96, 285, 10.1016/j.jconrel.2004.02.002 · DOI
  125. Chen, 2004, Synthesis and pH sensitivity of carboxymethyl chitosan-based polyampholyte hydrogels for protein carrier matrices, Biomaterials, 25, 3725, 10.1016/j.biomaterials.2003.09.100 · DOI
  126. Vaghani, 2012, Synthesis and characterization of pH-sensitive hydrogel composed of carboxymethyl chitosan for colon targeted delivery of ornidazole, Carbohydr. Res., 347, 76, 10.1016/j.carres.2011.04.048 · DOI
  127. Zhang, 2008, Synthesis of carboxymethyl-chitosan-bound magnetic nanoparticles by the spraying coprecipitation method, Scr. Mater., 59, 211, 10.1016/j.scriptamat.2008.03.006 · DOI
  128. Zhu, 2008, Suspension of Fe3O4 nanoparticles stabilized by chitosan and O-carboxymethyl chitosan, Int. J. Pharm., 350, 361, 10.1016/j.ijpharm.2007.09.004 · DOI
  129. Zheng, 2011, In vitro characterization and in vivo studies of crosslinked lactosaminated carboxymethyl chitosan nanoparticles, Carbohydr. Polym., 84, 1048, 10.1016/j.carbpol.2010.12.067 · DOI
  130. Zou, 2012, Octreotide-modified N-octyl-O, N-carboxymethyl chitosan micelles as potential carriers for targeted antitumor drug delivery, J. Pharm. Sci., 101, 627, 10.1002/jps.22798 · DOI
  131. Zhu, 2009, Interaction between Ocarboxymethylchitosan and dipalmitoyl-sn-glycero-3-phosphocholine bilayer, Biomaterials, 26, 6873, 10.1016/j.biomaterials.2005.05.021 · DOI
  132. Li, 2012, A pH sensitive multifunctional gene carrier assembled via layer-by-layer technique for efficient gene delivery, Int. J. Nanomedicine, 7, 925
  133. Maya, 2012, Efficacy of tetracycline encapsulated O-carboxymethyl chitosan nanoparticles against intracellular infections of Staphylococcus aureus, Int. J. Biol. Macromol., 51, 392, 10.1016/j.ijbiomac.2012.06.009 · DOI
  134. Huang, 2017, Intestine-targeted delivery potency of the O-carboxymethyl chitosan – gum Arabic coacervate: effects of coacervation acidity and possible mechanism, Mater. Sci. Eng. C Mater. Biol. Appl., 79, 423, 10.1016/j.msec.2017.05.074 · DOI
  135. Zheng, 2011, In vitro characterization, and in vivo studies of crosslinked lactosaminated carboxymethyl chitosan nanoparticles, Carbohydr. Polym., 84, 1048, 10.1016/j.carbpol.2010.12.067 · DOI
  136. Sun, 2017, Stability and activity of immobilized trypsin on carboxymethyl chitosan-functionalized magnetic nanoparticles cross-linked with carbodiimide and glutaraldehyde, J. Chromatogr. B Anal. Technol. Biomed. Life Sci., 1054, 57, 10.1016/j.jchromb.2017.04.016 · DOI
  137. Wei, 2016, Structure formation in pH-sensitive hydrogels composed of sodium caseinate and N, O-carboxymethyl chitosan, Int. J. Biol. Macromol., 89, 353, 10.1016/j.ijbiomac.2016.04.081 · DOI
  138. Kalliola, 2017, The pH sensitive properties of carboxymethyl chitosan nanoparticles cross-linked with calcium ions, Colloids Surf. B: Biointerfaces, 153, 229, 10.1016/j.colsurfb.2017.02.025 · DOI
  139. Sayın, 2009, TMC–MCC (N-trimethyl chitosan–mono-N-carboxymethyl chitosan) nanocomplexes for mucosal delivery of vaccines, Eur. J. Pharm. Sci., 38, 362, 10.1016/j.ejps.2009.08.010 · DOI
  140. Upadhyaya, 2013, Biomedical applications of carboxymethyl chitosans, Carbohydr. Polym., 91, 452, 10.1016/j.carbpol.2012.07.076 · DOI
  141. Xu, 2018, Carboxymethyl chitosan/gelatin/hyaluronic acid blended-membranes as epithelia transplanting scaffold for corneal wound healing, Carbohydr. Polym., 192, 240, 10.1016/j.carbpol.2018.03.033 · DOI
  142. Chen, 2002, The effect of carboxymethylchitosan on proliferation and collagen secretion of normal and keloid skin fibroblasts, Biomaterials, 23, 4609, 10.1016/S0142-9612(02)00207-7 · DOI
  143. Zhou, 2004, Reduction in postoperative adhesion formation and re-formation after an abdominal operation with the use of N,O-carboxymethyl chitosan, Surgery, 135, 307, 10.1016/j.surg.2003.07.005 · DOI
  144. Li, 2012, In situ injectable nano-composite hydrogel composed of curcumin, N,O-carboxymethyl chitosan and oxidized alginate for wound healing application, Int. J. Pharm., 437, 110, 10.1016/j.ijpharm.2012.08.001 · DOI
  145. Ruszczak, 2000, Modern aspects of wound healing: an update, Dermatol. Surg., 26, 219, 10.1046/j.1524-4725.2000.09215.x · DOI
  146. Huang, 2013, Influence of radiation crosslinked carboxymethyl-chitosan/gelatin hydrogel on cutaneous wound healing, Mater. Sci. Eng. C, 33, 4816, 10.1016/j.msec.2013.07.044 · DOI
  147. Chen, 2016, Preparation of porous carboxymethyl chitosan grafted poly (acrylic acid) superabsorbent by solvent precipitation and its application as a hemostatic wound dressing, Mater. Sci. Eng. C, 63, 18, 10.1016/j.msec.2016.02.048 · DOI
  148. Agarwal, 2016, Gelatin/carboxymethyl chitosan based scaffolds for dermal tissue engineering applications, Int. J. Biol. Macromol., 93B, 1499, 10.1016/j.ijbiomac.2016.04.028 · DOI
  149. Sharifi, 2018, Polycaprolactone/carboxymethyl chitosan nanofibrous scaffolds for bone tissue engineering application, Int. J. Biol. Macromol., 115, 243, 10.1016/j.ijbiomac.2018.04.045 · DOI
  150. Mattioli-Belmonte, 1999, N,N-dicarboxymethyl chitosan as delivery agent for bone morphogenetic protein in the repair of articular cartilage, Med. Biol. Eng. Comput., 37, 130, 10.1007/BF02513279 · DOI
  151. Shi, 2009, Functionalization of titanium with carboxymethyl chitosan and immobilized bone morphogenetic protein-2 for enhanced osseointegration, Biomacromolecules, 10, 1603, 10.1021/bm900203w · DOI
  152. Mishra, 2011, Enzymatically crosslinked carboxymethyl-chitosan/gelatin/nano-hydroxyapatite injectable gels for in situ bone tissue engineering application, Mater. Sci. Eng. C, 31, 1295, 10.1016/j.msec.2011.04.007 · DOI
  153. Jayakumar, 2009, Bioactive and metal uptake studies of carboxymethyl chitosangraft-d-glucuronic acid membranes for tissue engineering and environmental applications, Int. J. Biol. Macromol., 45, 135, 10.1016/j.ijbiomac.2009.04.016 · DOI
  154. Budiraharjo, 2012, Hydroxyapatite-coated carboxymethyl chitosan scaffolds for promoting osteoblast and stem cell differentiation, J. Colloid Interface Sci., 366, 224, 10.1016/j.jcis.2011.09.072 · DOI
  155. Zhou, 2012, Radiation synthesis of gelatin/CM-chitosan/β-tricalcium phosphate composite scaffold for bone tissue engineering, Mater. Sci. Eng. C, 32, 994, 10.1016/j.msec.2012.02.029 · DOI
  156. Tang, 2012, An improved complex gel of modified gellan gum and carboxymethyl chitosan for chondrocytes encapsulation, Carbohydr. Polym., 88, 46, 10.1016/j.carbpol.2011.11.058 · DOI
  157. Zhao, 2015, Antibacterial and conductive injectable hydrogels based on quaternized chitosan-graft-polyaniline/oxidized dextran for tissue engineering, Acta Biomater., 26, 236, 10.1016/j.actbio.2015.08.006 · DOI
  158. Zheng, 2015, Bifunctional coating based on carboxymethyl chitosan with stable conjugated alkaline phosphatase for inhibiting bacterial adhesion and promoting osteogenic differentiation on titanium, Appl. Surf. Sci., 360A, 86
  159. Yap, 2016, Evaluation of hydrogel composing of Pluronic F127 andcarboxymethyl hexanoyl chitosan as injectable scaffold for tissueengineering applications, Colloids Surf. B: Biointerfaces, 146, 204, 10.1016/j.colsurfb.2016.05.094 · DOI
  160. Yin, 2017, Itaconic acid grafted carboxymethyl chitosan and its nanoparticles: preparation, characterization and evaluation, Int. J. Biol. Macromol., 102, 10, 10.1016/j.ijbiomac.2017.04.005 · DOI
  161. Xie, 2005, CdSe/ZnS labeled carboxymethyl chitosan as a bioprobe for live cell imaging, Chem. Comm., 0, 5518, 10.1039/b509781a · DOI
  162. Shi, 2009, (Carboxymethyl)chitosan-modified superparamagnetic iron oxide nanoparticles for magnetic resonance imaging of stem cells, Appl. Mater. Interfaces, 1, 328, 10.1021/am8000538 · DOI
  163. Bhattacharya, 2011, Folate receptor targeted, carboxymethyl chitosan functionalized iron oxide nanoparticles: a novel ultradispersed nanoconjugates for bimodal imaging, Nanoscale, 3, 1653, 10.1039/c0nr00821d · DOI
  164. Dalia, 2011, Watersoluble derivatives of chitosan as a target delivery system of 99mTc to some organs in vivo for nuclear imaging and biodistribution, J. Radioanal. Nucl. Chem., 290, 557, 10.1007/s10967-011-1310-9 · DOI
  165. Tan, 2012, Novel quantum dots–carboxymethyl chitosan nanocomposite nitric oxide donors capable of detecting release of nitric oxide in situ, Acta Biomater., 8, 3744, 10.1016/j.actbio.2012.06.008 · DOI
  166. Kohsari, 2016, Antibacterial electrospun chitosan–polyethylene oxidenano composite mats containing bioactive silver nanoparticles, Carbohydr. Polym., 140, 287, 10.1016/j.carbpol.2015.12.075 · DOI
  167. Kohsari, 2016, Antibacterial electrospun chitosan-polyethylene oxide nanocomposite mats containing ZIF-8 nanoparticles, Int. J. Biol. Macromol., 91, 778, 10.1016/j.ijbiomac.2016.06.039 · DOI
  168. Shariatinia, 2015, Mechanical properties and antibacterial activities of novel nanobiocomposite films of chitosan and starch, Food Hydrocoll., 46, 112, 10.1016/j.foodhyd.2014.12.026 · DOI
  169. Shariatinia, 2017, Controlled release of metformin from chitosan–based nanocomposite films containing mesoporous MCM-41 nanoparticles as novel drug delivery systems, J. Colloid Interface Sci., 501, 60, 10.1016/j.jcis.2017.04.036 · DOI
  170. Shariatinia, 2013, Synthesis and antibacterial activities of novel nanocomposite films of chitosan/phosphoramide/Fe3O4 NPs, Int. J. Biol. Macromol., 60, 226, 10.1016/j.ijbiomac.2013.05.026 · DOI
  171. Shariatinia, 2015, Antibacterial activities of novel nanocomposite biofilms of chitosan/phosphoramide/Ag NPs, Polym. Compos., 36, 454, 10.1002/pc.22960 · DOI
  172. Chen, 2017, Quaternized carboxymethyl chitosan/organic montmorillonite nanocomposite as a novel cosmetic ingredient against skin aging, Carbohydr. Polym., 173, 100, 10.1016/j.carbpol.2017.05.088 · DOI
  173. Jimtaisong, 2014, Utilization of carboxymethyl chitosan in cosmetics, Int. J. Cosmet. Sci., 36, 12, 10.1111/ics.12102 · DOI
  174. Pillai, 2005, Ultraviolet radiation and skin aging: roles of reactive oxygen species, inflammation and protease activation, and strategies for prevention of inflammation-induced matrix degradation—a review, Int. J. Cosmet. Sci., 27, 17, 10.1111/j.1467-2494.2004.00241.x · DOI · Paper page
  175. Polaskova, 2013, Moisturizing effect of topical cosmetic products applied to dry skin, J. Cosmet. Sci., 64, 329
  176. Muzzarelli, 1988, Carboxymethylated chitins and chitosans, Carbohydr. Polym., 8, 1, 10.1016/0144-8617(88)90032-X · DOI
  177. Chen, 2002, Relationship between molecular structure and moisture-retention ability of carboxymethyl chitin and chitosan, J. Appl. Polym. Sci., 83, 1233, 10.1002/app.2290 · DOI
  178. Chen, 2003, Relationships between the molecular structure and moisture-absorption and moisture-retention abilities of carboxymethyl chitosan: II. Effect of degree of deacetylation and carboxymethylation, Carbohydr. Res., 338, 333, 10.1016/S0008-6215(02)00462-7 · DOI
  179. Muzzarelli, 2002, N-carboxymethyl chitosan in innovative cosmeceutical products, J. Appl. Cosmetol., 20, 201
  180. Feng, 2015, Surface charge effect on mucoadhesion of chitosan based nanogels for local anti-colorectal cancer drug delivery, Colloids Surf. B: Biointerfaces, 128, 439, 10.1016/j.colsurfb.2015.02.042 · DOI

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Metadata

Authors
Shariatinia, Z.
Venue
International Journal of Biological Macromolecules
Publisher
Elsevier BV
Published
2018-12
Volume
120
Pages
1406-1419
ISSN
0141-8130
DOI
10.1016/j.ijbiomac.2018.09.131
Cited by
777
References
3
Language
en
Licence
Funders
Amirkabir University of Technology

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