Design Polysaccharides of Marine Origin: Chemical Modifications to Reach Advanced Versatile Compounds
Jean Le Bideau,
Polysaccharides are among the most abundant macromolecules on Earth. These polymers are easily obtained from various marine
resources such as algae, microorganisms and crustacean shells. The structure of these natural carbohydrates is innovative and quite
complex. Marine biopolymers represent key scaffolds toward large challenging fields, such as biomedical applications (glycosaminoglycans,
regenerative medicine and drug delivery) and tailored biomaterials. Chemical modifications can be applied to modify their final
properties in a specific purpose. New functional glycans are achievable and represent a real potential with their intrinsic biocompatibility
Hydroxyl groups are ubiquitous in polysaccharides structure and involved in most of the chemical modifications. The most useful functionalities
are ester, ether, amide, amine and alkyl groups. The starting materials could be a natural or depolymerized polymers and the
reaction considered with a regioselective point of view.
In this review, we will focus on chitin polysaccharide, which is extracted according to industrial processing from exoskeleton of several
marine crustaceans. A subsequent deacylation provides chitosan. This marine polysaccharide is very similar to cellulose, a widespread fiber
plant organic polymer, except for an amine group on the C2 position instead of a hydroxyl group. Furthermore, seaweeds provide the
most abundant sources of polysaccharides: alginates, agar/agarose, carrageenans and fucoidans. In order to improve the original physicochemical
and biochemical properties, we will highlight the chemical modifications involving the listed marine polysaccharides of interest.
Keywords: Alginates, carrageenans, chemical modification, chitin, chitosan, grafting, marine polysaccharide, polymer.
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