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Interaction Between Chitosan and Mucin: Fundamentals and Applications
Abstract
The term chitosan (CS) refers to a family of aminopolysaccharides derived from chitin. Among other properties, CS is nontoxic, mucoadhesive and can be used for load and transport drugs. Given these and other physicochemical and biological properties, CS is an optimal biopolymer for the development of transmucosal drug delivery systems, as well as for the treatment of pathologies related to mucosal dysfunctions. Mucins are glycoprotein macromolecules that are the major components of mucus overlaying epithelia. CS interacts with mucin and adsorbs on and changes the rheology of mucus. However, CS and mucins denote families of polymers/macromolecules with highly variable chemical structure, properties, and behavior. To date, their interactions at the molecular level have not been completely unraveled. Also, the properties of complexes composed of CS and mucin vary as a function of the sources and preparation of the polymers. As a consequence, the mucoadhesion and drug delivery properties of such complexes vary as well. The breadth of this review is on the molecular interactions between CS and mucin. In particular, in vitro and ex vivo characterization methods to investigate both the interactions at play during the formation of CS-mucin complexes, and the advances on the use of CS for transmucosal drug delivery are addressed.
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![Figure 1 Structure of the mucus gel on the epithelial surfaces. Reprinted from [1], with permission from Elsevier.](/paper-figures/62ca9c6772bb4e6bada5880f53e15ccb/interaction-between-chitosan-and-mucin-fundamentals-and-applications-figure-1.jpg)
![Figure 2 The domain structure of mucins. VWD: Von Wiellebrand D-domain, C8: conserved cysteine rich domain, TIL: trypsin inhibitor-like cystein-rich domain, CysD: domain rich in cystein residues, VWC: Von Wiellebrand C-domain, PTS: PTS domains, CK: cystein knot domain, NIDO: nidogen homology region, AMOP: the adhesion-associated domain in MUC4 and other proteins, SEA: sea-urchin sperm protein, enterokinase, and agrin domain, TM: transmembrane domain. Reprinted with permission from Springer Nature, Copyright 2016 [2].](/paper-figures/bed1dad2e19745c9b679ce79c18c1db8/interaction-between-chitosan-and-mucin-fundamentals-and-applications-figure-2.jpg)
![Figure 3 Representation of the crosslinking of mucins. Extracted with permission from [1].](/paper-figures/2654d0c51cb147318f7397becd1fbe14/interaction-between-chitosan-and-mucin-fundamentals-and-applications-figure-3.jpg)



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“Several intrinsic factors have effects on the interaction between chitosan nanocarriers and mucins specially that related to the nature of the polymer such as the molecular weight and surface charge of CSNPs.131”
From Current Advances in Chitosan Nanoparticles Based Oral Drug Delivery for Colorectal Cancer Treatment (2022) · cites this paper as [131]
In the citing paper
“On the other hand, mucins are glycoproteins with pI between 2 and 3, therefore they will be charged negatively in medium pH > pI, promoting electrostatic interaction between mucins and chitosan especially at pH between 2.4 and 6.3.131”
From Current Advances in Chitosan Nanoparticles Based Oral Drug Delivery for Colorectal Cancer Treatment (2022) · cites this paper as [131]
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Metadata
- Authors
- Collado-González, M., González Espinosa, Y., & Goycoolea, F. M.
- Venue
- Biomimetics
- Publisher
- MDPI AG
- Published
- 2019-04-25
- Volume
- 4
- Issue
- 2
- Pages
- 32
- ISSN
- 2313-7673
- PMC
- PMC6631199
- Cited by
- 160
- References
- 1
- Language
- en
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