Chitosan protein

This chapter gives a general introduction to the book and describes briefly the context for which the editors established its contents and explains why certain topics were excluded from it. It covers the main raw materials based on vegetable resources, namely (i) wood and its main components cellulose, lignin, hemicelluloses, tannins, rosins and terpenes, as well as species-speciflc constituents, like natural rubber and suberin and (ii) annual plants as sources of starch, vegetable oils, hemicelluloses, mono and disaccharides and algae. Then, the main animal biomass constituents are briefly described, with particular emphasis on chitin, chitosan, proteins and cellulose whiskers from molluscs. Finally, bacterial polymers such as poly(hydroxyalkanoates) and bacterial cellulose are evoked. For each relevant renewable source, this survey alerts the reader to the corresponding chapter in the book. 

Animal biomass. Vegetal biomass. Wood, Cellulose, Lignins, Hemicelluloses, Natural rubber, Suberin, Tannins, Rosins, Terpenes, Annual plants. Starch, Vegetable oils, Hemicelluloses, Mono and disaccharides, Polylactic acid. Algae, Chitin, Chitosan, Proteins, Cellulose whiskers. Bacterial polymers. Poly (hydro xyalkanoates). Bacterial cellulose... 

Approach 3 Insights into multipurpose chitosan/protein-based gels as functional biomaterial drug-delivery prototypes. 

There are many polymers that are suitable for the production of nanoparticles employed for drug delivery, which can generally be divided into two groups natural polymers, e.g., polysaccharides (chitosan), proteins (albumin, gelatin), as well as synthetic polymers, e.g., polyesters (poly(lactic add), poly(glycolic add), poly(hydroxy butyrate), poly-e-caprolactone, poly-p-malic add, poly(dioxanones)) polyanhydrides (poly(adipic add)) polyamides (poly(amino acids)) phosphorous-based polymers (polyphosphate) poly(cyano acrylates) polyurethanes polyortho esters and polyacetals. Extreme attention has to be paid to the biodegradability and biocompatibility of the polymers. It is essential that polymers used for medical applications are not detrimental for the tissue or cells and that they can be easily decomposed into simple harmless molecules and eliminated by the human body [ 18-22]. 

The use of other proteins, such as gelatin, collagen, etc., to prepare chitosan blended membranes was tried in a 7 3 ratio (chitosan protein) and the results were compared to the standard cellulose membranes. The permeability, as a function of time, of various molecules, such as urea, creatinine, uric acid, glucose and albumin, through such membranes is shown in Figures 13, 14, 15, 16 and 17, respectively. It appears that the protein blended membranes exhibited improved permeability properties with respect to small molecules compared to the standard cellulose membrane or bare chitosan. These protein blended membranes... 

Natural pol5miers are formed in nature during the growth cycles of all organisms. Natural biodegradable polymers are called biopolymers or renewable polymers. There are two main types of biopolymers those that come from renewable resources and those that need to be polymerized but come from renewable resources. Therefore, the first type includes potysaccharide (starch, chitosan), protein (keratin, soy protein, etc.) the second type includes potylactic acid (Tang et al., 2012). 

For the preparation of nanoparticles based on two aqueous phases at room temperature one phase contains chitosan and poly(ethylene oxide) and the other contains sodium tripolyphosphate. The particle size (200-1000 nm) and zeta potential (between -i- 20 mV and -l- 60 mV) could be modulated by varying the ratio chitosan/PEO-PPO. These nanoparticles have great proteinloading capacity and provide continuous release of the entrapped protein (particularly insulin) for up to one week [100,101]. 

The cell growth was much faster on the chitosan-hydroxyapatite scaffolds with the glass than on the chitosan-hydroxyapatite scaffold without the glass. The total protein content of cells increased over time on both composites. The cells on the chitosan-hydroxyapatite-glass also expressed significantly higher amount of alkaline phosphatase at days 7 and 11 and osteocalcin at day 7 than those on chitosan-hydroxyapatite [165]. 

In most cases the microspheres were insoluble. The polysaccharides might be partially cross-linked via amido groups formed by the carboxyl groups of the polyanion and the restored free amino group of chitosan. The susceptibility to enzymatic hydrolysis by lysozyme was poor, mainly because lysozyme, a strongly cationic protein, can be inactivated by anionic polysaccharides [207]. 

Chenite et al. reported on thermosensitive chitosan gels for encapsulating living cells and therapeutic proteins they are liquid below room temperature but form monolithic gels at body temperature [220-223]. 

The nasal tissue is highly vascularized and provides efficient systemic absorption. Compared with oral or subcutaneous administration, nasal administration enhances bioavailability and improves safety and efficacy. Chitosan enhances the absorption of proteins and peptide drugs across nasal and intestinal epithelia. Gogev et al. demonstrated that the soluble formulation of glycol chitosan has potential usefulness as an intranasal adjuvant for recombinant viral vector vaccines in cattle [276]. 

Works where study the hydrodynamic properties of a biopolymers in aqueous solution at different temperatures are made by Guner (1999), and Guner Kibarer (2001) for dextran Ghen Tsaih (1998) and Kasaii (2008) for chitosan, Bohidar for gelatin (1998), and Monkos for serum proteins (1996,1997,1999, 2000, 2004 and 2005). 

Fig. 6. Effect of the degree of chitin acetylation (%) on the interaction between chitin and chitin-specific wheat POs (A) (U/ mg protein) (Maksimov et al., 2005) (B) PAAG after lEF of PO fractions from wheat roots (a) not bound to high-acetylated (b) and low-acetylated chitosan (c) (Khairullin et al., 2000). Designations (1) 12% (2) 23% (3) 37% (4) 45% (5) 65%.

Protein isolation with affinity precipitation has been discussed in detail by Mattiasson and co-workers (see, e.g. Galaev and Mattiassion, 1997) and they have provided an exhaustive tabulation. Polymers varied from alginate.s/chitosan to dextran to NIPAM. Examples of the used proteins are from trypsin, p-glucosidase, xylanase, alkaline protease, etc. It is remarkable that affinity precipitation can sometimes give results comparable to affinity chromatography. 

Bio-nanocomposites based on calcium phosphates can perform other innovative fundions such as acting as a reservoir for the controlled release of bioadive compounds once the material is implanted in the bone defect. For instance, the incorporation of a morphogenetic protein that promotes bone regeneration in an HAP-alginate-collagen system [110] or a vitamin in a Ca-deficient HAP-chitosan nanocomposite [111] are recent examples of this kind of application. 

J.J. Feng, G. Zhao, J.J. Xu, and H.Y. Chen, Direct electrochemistry and electrocatalysis of heme proteins immobilized on gold nanoparticles stabilized by chitosan. Anal. Biochem. 342, 280-286 (2005). 

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