Handbook of Polymers for Pharmaceutical Technologies 2015
DOI: 10.1002/9781119041450.ch9
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Current State of the Potential Use of Chitosan as Pharmaceutical Excipient

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Cited by 3 publications
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“…Due to the presence of free amino groups that can protonate at a pH below 6 (Chicatun et al, 2017;Leedy et al, 2011), CS forms with acids water-soluble salts (Ravi Kumar et al, 2004). The solubility of chitosan depends on the degree of deacetylation (DD) and the molecular weight of the polysaccharide (Madureira et al, 2015;Wang et al, 2020b). Due to its positive charge, chitosan can form complexes with negatively charged compounds, e.g.…”
Section: Physicochemical Propertiesmentioning
confidence: 99%
“…Due to the presence of free amino groups that can protonate at a pH below 6 (Chicatun et al, 2017;Leedy et al, 2011), CS forms with acids water-soluble salts (Ravi Kumar et al, 2004). The solubility of chitosan depends on the degree of deacetylation (DD) and the molecular weight of the polysaccharide (Madureira et al, 2015;Wang et al, 2020b). Due to its positive charge, chitosan can form complexes with negatively charged compounds, e.g.…”
Section: Physicochemical Propertiesmentioning
confidence: 99%
“…35 To characterise chitosan, its viscosity is often used, which depends on various parameters such as concentration of chitosan in the solution, temperature, degree of deacetylation. 36 The cationic nature of chitosan distinguishes it from other natural polysaccharides. Due to its positive charge, chitosan has the ability to form complexes with negatively charged compounds, e.g.…”
Section: Physicochemical Propertiesmentioning
confidence: 99%