Smart Materials 2008
DOI: 10.1201/9781420043730.ch10
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Chitosan-Based Gels and Hydrogels

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Cited by 5 publications
(6 citation statements)
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“…The process of electrode coating was as follows: First, 10 μL of –COOH‐MWCNTs/CS dispersion was placed on the electrode, and left to dry for 1 H. After solvent evaporation, 10 μL of CS solution was dropped on the electrode surface and solvent again evaporated at room temperature in air for approximately 1 H. Then, 10 μL of 0.1 M phosphate buffer saline (PBS, pH 7.0) solution was added on the surface and left to dry for 40 Min, and this step was then repeated; the purpose being to deprotonate the amino groups of CS by changing the pH at the electrode surface. When pH values are in the vicinity of the p Ka of CS ( p Ka = 6.5), amino groups of CS are deprotonated . Finally, EDC/NHS coupling was used to covalently cross‐link COOH‐MWCNT to the CS polymer and formed on the surface: 10 μL EDC (0.5%, m/v) and NHS (0.5%, m/v) in the same buffer solution was dropped on the surface and left to dry for 2 H. …”
Section: Methodsmentioning
confidence: 99%
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“…The process of electrode coating was as follows: First, 10 μL of –COOH‐MWCNTs/CS dispersion was placed on the electrode, and left to dry for 1 H. After solvent evaporation, 10 μL of CS solution was dropped on the electrode surface and solvent again evaporated at room temperature in air for approximately 1 H. Then, 10 μL of 0.1 M phosphate buffer saline (PBS, pH 7.0) solution was added on the surface and left to dry for 40 Min, and this step was then repeated; the purpose being to deprotonate the amino groups of CS by changing the pH at the electrode surface. When pH values are in the vicinity of the p Ka of CS ( p Ka = 6.5), amino groups of CS are deprotonated . Finally, EDC/NHS coupling was used to covalently cross‐link COOH‐MWCNT to the CS polymer and formed on the surface: 10 μL EDC (0.5%, m/v) and NHS (0.5%, m/v) in the same buffer solution was dropped on the surface and left to dry for 2 H. …”
Section: Methodsmentioning
confidence: 99%
“…Then, 10 μL of 0.1 M phosphate buffer saline (PBS, pH 7.0) solution was added on the surface and left to dry for 40 Min, and this step was then repeated; the purpose being to deprotonate the amino groups of CS by changing the pH at the electrode surface. When pH values are in the vicinity of the p Ka of CS ( p Ka = 6.5), amino groups of CS are deprotonated .…”
Section: Methodsmentioning
confidence: 99%
“…In the medical field, pure chitosan films have been employed for wound dressings, drug delivery systems, and medical device coatings due to their antimicrobial, biocompatible, and biodegradable properties [24].…”
Section: Use In Medicinementioning
confidence: 99%
“…At the same time, for alkaline deacetylation, a degree of deacetylation of 10-20% is considered a great success. In addition, alkaline deacetylation leads to partial depolymerization of the polysaccharide [24]. Once chitosan is synthesized, it can be further processed to form films through various techniques (Figure 2):…”
mentioning
confidence: 99%
“…Chitosan is a modified natural cationic polymer composed of β-(1→4)-linked Dglucosamine residues, obtained by partial N-deacetylation of chitin (Figure 1). This polyaminosaccharide polymer has polycationic characteristics, due to the presence of numerous amino groupings (ALVES; MANO, 2008;ANITHA et al, 2011b), and possesses excellent chemical and biological properties, making it very attractive for applications in many areas such as, biology, chemistry, pharmacy, medicine, agriculture, food, environmental (YAO et al, 2011;KASHYAP;HEIDEN, 2015a).…”
Section: Introductionmentioning
confidence: 99%