Chitosan molecular structure as a function of N-acetylation

• Published in: Biopolymers Vol. 95; no. 7; pp. 448 - 460
• Main Authors: Franca, Eduardo F., Freitas, Luiz C. G., Lins, Roberto D.
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.07.2011
• Subjects: 08 HYDROGEN; ACETYLATION; Biopolymers; CHAINS; CHITIN; Chitosan; Chitosan - chemistry; DISTRIBUTION; ELECTROSTATICS; Environmental Molecular Sciences Laboratory; FLEXIBILITY; HYDROGEN; Hydrogen Bonding; Molecular Conformation; MOLECULAR STRUCTURE; nanoparticle; Nanoparticles - chemistry; Nanostructure; ORIENTATION; POLYSACCHARIDES; Reproduction; salvation; SOLUBILITY; SOLVATION; SPATIAL DISTRIBUTION; STABILITY; SWELLING; WATER
• ISSN: 0006-3525; 1097-0282; 1097-0282
• DOI: 10.1002/bip.21602

Molecular dynamics simulations have been carried out to characterize the structure and solubility of chitosan nanoparticle‐like structures as a function of the deacetylation level (0, 40, 60, and 100%) and the spatial distribution of the N‐acetyl groups in the particles. The polysaccharide chains of highly N‐deacetylated particles where the N‐acetyl groups are uniformly distributed present a high flexibility and preference for the relaxed two‐fold helix and five‐fold helix motifs. When these groups are confined to a given region of the particle, the chains adopt preferentially a two‐fold helix with ϕ and ψ values close to crystalline chitin. Nanoparticles with up to 40% acetylation are moderately soluble, forming stable aggregates when the N‐acetyl groups are unevenly distributed. Systems with 60% or higher N‐acetylation levels are insoluble and present similar degrees of swelling regardless the distribution of their N‐acetyl groups. Overall particle solvation is highly affected by electrostatic forces resulting from the degree of acetylation. The water mobility and orientation around the polysaccharide chains affects the stability of the intramolecular O3‐HO3(n)···O5(n +1) hydrogen bond, which in turn controls particle aggregation. © 2011 Wiley Periodicals, Inc. Biopolymers 95: 448–460, 2011.