Polysaccharides biodegradability

Hydro-biodegradation. Most organic polymers are much more hydrophobic than those found in nature, and living organisms have not evolved enzymes which can effectively penetrate and cleave them. Polymers which resist hydrolysis are also resistant to biodegradation, since enzymes operate in aqueous media. Thus synthetic polymers are typically much more resistant to biological attack than are the natural polymers, such as proteins and polysaccharides. Biodegradability of polymers has been well reviewed (see eg. Refs. 166-169). 

Oxidation of polysaccharides is a far more attractive route to polycarboxylates, potentially cleaner and less cosdy than esterification. Selectivity at the 2,3-secondary hydroxyls and the 6-primary is possible. Total biodegradation with acceptable property balance has not yet been achieved. For the most part, oxidations have been with hypochlorite—periodate under alkaline conditions. In the 1990s, catalytic oxidation has appeared as a possibiUty, and chemical oxidations have also been developed that are specific for the 6-hydroxyl oxidation. 

Biodegradable films made from edible biopolymers from renewable sources could become an important factor in reducing the environmental impact of plastic waste. Proteins, lipids, and polysaccharides are the main biopolymers employed to make edible films and coatings. Which of these components are present in different proportions and determine the properties of the material, as a barrier to water vapor, oxygen, carbon dioxide, and lipid transfer in food systems (Gomez-Guillen et al. 2002 and 2009). 

Biodegradable drilling fluid formulations have been suggested. These are formulations of a polysaccharide in a concentration insufficient to permit a contaminating bacterial proliferation, namely a high-viscosity carboxymethyl-cellulose sensitive to bacterial enzymes produced by the degradation of the polysaccharide [1419]. 

Probably the most promising polymeric drug carrier system involves polysaccharide molecules. These are natural polymers and are often biodegradable to products that are useful to the host or easily eliminated by the host. Dextrans have been the most extensively used polysaccharide for macromolecular prodrug preparations (79). These materials are biocompatible and the in vivo fate is directly related to their molecular weight. Moreover these macromolecules can be easily targetted to the hepatocytes with D-mannose or L-fucose (20). 

Carboxylic Acids Obtained by Fermentation of Carbohydrates Lactic (2-hydroxy-propionic) acid obtained by fermentation of glucose and polysaccharides is used by NatureWorks (Cargill/Dow LLC) to prepare polylactide (PLA), a biodegradable or recyclable polymer with a potential production of 140000 t a-1 (Scheme 3.4) [23], This and other potential useful reactions from lactic acid have been reviewed by Datta and Henry [24],... 

A special group of carrier-linked prodrugs are the site-specific chemical delivery systems [23], Macromolecular prodrugs are synthetic conjugates of drugs covalently bound (either directly or via a spacer) to proteins, polypeptides, polysaccharides, and other biodegradable polymers [24],... 

There are 22 chapters in the book and they cover the most important aspects of polymers as drugs, prodrugs, dmg delivery systems, and in situ prostheses. The major features promulgated are synthesis, derivatization, degradation, characterization, application, and evaluation techniques as well as new biodegradable materials, assemblies, hydrogels, telechelic polymers, derivatized polysaccharides, micro- and nanoparticles, mimetic... 

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