Chitin and Chitosan 2019
DOI: 10.1002/9781119450467.ch3
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Physicochemical Properties of Chitosan and its Degradation Products

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Cited by 18 publications
(9 citation statements)
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“…The physicochemical properties of chitosan define the relationship that exists between the chemical structure of chitosan and its uses in many branches of science and industry ( Figure 2 ). Deacetylation degree (DD), average molar mass, solubility, crystallinity, viscosity and content of water are the most frequently evaluated properties [ 61 , 62 , 63 ].…”
Section: Chitosan As a Matrix For Nanosystemspreparation: Methodsmentioning
confidence: 99%
“…The physicochemical properties of chitosan define the relationship that exists between the chemical structure of chitosan and its uses in many branches of science and industry ( Figure 2 ). Deacetylation degree (DD), average molar mass, solubility, crystallinity, viscosity and content of water are the most frequently evaluated properties [ 61 , 62 , 63 ].…”
Section: Chitosan As a Matrix For Nanosystemspreparation: Methodsmentioning
confidence: 99%
“…CS is a natural mucopolysaccharide that has a very similar chemical structure to cellulose, with one acetylamino functional group instead of a hydroxyl group present at the C-2 position. Pure CS itself exhibits different biological properties, as summarized in Table 2 [39][40][41][42][43][44][45][46][47][48]. For commercial production, CS is manufactured by the alkaline Ndeacetylation of chitin.…”
Section: Chitosan: Source and Structurementioning
confidence: 99%
“…The soluble degraded product of CS can effectively inhibit Lucerne mosaic virus and tobacco mosaic virus. [40,41] Antifungal CS derivatives with a large charge density can effectively inhibit different fungi such as Candida albicans and Candida parapsilosis. [39,42] Wound healing Pure CS is widely used as a wound dressing material due to its excellent wound healing activity.…”
Section: Antiviralmentioning
confidence: 99%
“…In the group of substitution reactions, i.e., the introduction of side groups to the chitosan chain according to various types of reaction mechanisms, there are reactions such as alkylation, acylation, arylation, thiolation, sulfonation, or phosphorylation, etc. [ 36 , 37 , 38 , 39 , 40 , 41 , 42 , 43 , 44 , 45 , 46 , 47 , 48 ]. The most frequently studied chitosan derivatives are carboxymethyl chitosan [ 45 , 49 ].…”
Section: Introductionmentioning
confidence: 99%