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Schematic representation of a casein micelle. Source: http://openwetware.org/ wiki/User:Anthony_Salvagno/Notebook/Research/2009/11/11/Andy's_Poster. Last accessed 08/01/2014. 

Schematic representation of a casein micelle. Source: http://openwetware.org/ wiki/User:Anthony_Salvagno/Notebook/Research/2009/11/11/Andy's_Poster. Last accessed 08/01/2014. 

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Biopolymer-based nanostructures or microstructures can be fabricated with different compositions, structures, and properties so that colloidal delivery systems can be tailored for specific applications. These structures can be assembled using various approaches, including electrospinning, coacervation, nanoprecipitation, injection, layer-by-layer d...

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... structures that encapsulate cal- cium phosphate, which is essential for proper growth and functioning of infants. The core of the casein micelles is primarily formed by αs1-, αs2-, and β-caseins, while the outer layer consists of κ-casein, which helps stabilize them by generating a strong steric repulsion (Kaya-Celiker & Mallikarjunan, 2012; Fig. 3). Casein micelles can be produced in vitro by self-assembly of the casein units around a hydrophobic compound. Different salts (such as potas- sium phosphate, calcium chloride, and/or potassium citrate) are used to cre- ate the proper pH and ionic strength conditions to encapsulate the hydrophobic compound (Semo, Kesselman, Danino, & ...

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... Moreover, biopolymers are promising candidates for materials used in biotechnology applications because they tend to be compatible with diverse types of cells and tissues. In addition, they can be modified in a wide range of manners, which raises their applicability, in addition to being biodegradable and originating from renewable materials [1]. Among the natural polymers that have biotechnological potential, starch can be highlighted, particularly for its physical, chemical, and biological characteristics. ...
... It is a polysaccharide that is composed of two polymers, amylose, a linear polymer, and amylopectin, and has highly branched chains [15]. Amylose is a mainly linear polymer that consists of α (1,4) linked D-glucopyranosyl units, while amylopectin is a branched polymer of α-D-glucopyranosyl units that are primarily linked by (1,4) bonds with branches resulting from (1,6) linked D-glucopyranosyl units [16]. ...
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... Proteins can form nanocarriers with polysaccharides, emulsifiers, and other proteins through non-covalent interactions, such as van der Waals forces, hydrogen bonds, hydrophobic effects, and electrostatic interactions. 62 The range and intensity of these non-covalent interactions can be adjusted by the variations of the solvent type, solution concentration, temperature, pH, ionic strength, etc. These non-covalent interactions can bind the components together and maintain a certain degree of stability in the PNs. ...
... Under the influence of gravitational factors, acid, base, salt ions, temperature, and other factors in the solution, the PN is susceptible to aggregation, thereby reducing the physical stability. 62 Gravitational separation is driven by the density difference between the continuous phase and the dispersed phase. It can be slowed down by decreasing the particle diameter, reducing the density difference between the continuous phase and dispersed phase, and increasing the viscosity of continuous phase. ...
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... However, at pKa < pH < pI, complex coacervation could occur due to the strong electrostatic attraction, and the complete neutralization of biopolymer charges ( Weinbreck et al., 2003;Perez et al., 2014). This condition drives to associative phase separation, being one phase rich in both biopolymers and the other rich in solvent ( Davidov-Pardo et al., 2015;Niu et al., 2014). Moreover, when pH is reduced too far, the coacervates precipitate, because they become closely packed together. ...
... Moreover, when pH is reduced too far, the coacervates precipitate, because they become closely packed together. Lastly, when pH < pKa cosolubility condition is newly reached due to the loss of charges of the polysaccharides ( Davidov-Pardo et al., 2015). Associative phase separation involves both complex coacervation and precipitation. ...
... associative phase separation was not registered (as can be seen in Fig. 3), cosolubility phenomenon could be proposed at these conditions. This behavior can be explained by a great repulsion among biopolymer net charges ( Davidov-Pardo et al., 2015). However, at pH < 6.0 mixed systems showed phase separation after 24 h ( Fig. 3), suggesting that the observed turbidity could be related to the formation of big particles which sediment. ...
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This paper gives experimental information about the application of protein-polysaccharide associative phase separation to produce a dried ingredient (powder) of linoleic acid (LA). Powder production process consisted in: (i) LA binding to a well-characterized ovalbumin nanosized heat-induced aggregate (OVAn) to form LA-OVAn complexes in solution, (ii) polysaccharides (PS) addition to promote the associative phase separation of LA-OVAn complexes, and (iii) freeze-drying of the precipitated phase in order to obtain LA-OVAn-PS powders. For this, OVAn and anionic PS (gum Arabic -GA- and high methoxyl pectin -HMP-) mixed systems were studied at different OVAn-PS concentration ratio (ROVAn:PS) and aqueous medium pH by means of a complementary techniques set: optical density at 400 nm (as a measure of turbidity), zeta potential and biopolymer phase composition determination. Biopolymer associative phase separation process was described in terms of OVAn and PS separation yield (YOVAn and YPS, respectively) and PS content necessary to precipitate OVAn (PSp). YOVAn and PSp results suggest that ROVAn:PS 1:1 and 2:1 for OVAn-GA and OVAn-HMP systems, respectively, and pH 3.0 were the most suitable conditions to obtain LA-OVAn-PS freeze-dried powders. Powders water dispersibility and LA oxidative stability were evaluated over 13 days (expressed as non-deteriorated LA percent -LAND-). Results revealed that water dispersion behavior of LA-OVAn-HMP powder was better than LA-OVAn-GA; besides it has the highest LAND (∼80%) at the 13 day. These experimental findings highlighted that OVAn-PS associative phase separation was a convenient strategy, besides this information could be relevant to produce a LA functional ingredient.
... Formation of soluble complexes typically occurs at low ratios of protein to polysaccharide, and at moderate ionic strengths, i.e. under conditions where biopolymers have low charge densities or when pH is relatively far from the proteinʹs pI. For example, for a protein-anionic polysaccharide combination at pH values somewhat greater than the pI, net charges of both protein and polysaccharide are identical and form soluble complexes (Fig. 1, Davidov-Pardo, Joye, & McClements, 2015 ). Under these conditions , few charged moieties are accessible on each molecule and less protein can interact with the polysaccharide to cause charge neutralization. ...
... As well, there exist narrow pH and ionic strength ranges ensuring complexes stability. It is possible to stabilize the complexed coacervate structures by a convenient heat cure, and/or enzymatic treatment (Davidov-Pardo et al., 2015; de Kruif, Weinbreck, de Vries, 2004; Jones, 2014; Turgeon & Laneuville, 2009). An appropriate heat treatment above the denaturation temperature of protein which induced protein-protein interactions was applied to stabilize whey proteins-xanthan gum and whey proteins-pectin complexes. ...
... In another work, the enzyme transglutaminase was added to low methoxy pectin-caseinate system to cross-link caseinate and promote matrix gelation (Zhang, Decker, & Fig. 1. Example of complex coacervation in a solution containing a globular protein and an anionic polysaccharide (Davidov-Pardo et al., 2015). Plant phenolics were also used to cross-link gelatin-pectin coacervates. ...
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Biopolymeric microgels made of proteins and/or polysaccharides provide a renewable source for enteral nutrition, interface stabilization, controlled release applications and etc. These microgels consist of physically, chemically, or enzymatically cross-linked biopolymer molecules that trap and hold water within the particle network. They can be formed from single or mixed biopolymers using a variety of methods based on molecular association mechanisms and mechanical processes. Biopolymer type and microgelation method determine the main properties of resulting microgels. Certain challenges associated with the small dimensions of microgels can be addressed through the development of immobilized microgel matrices, in which individual microgel particles are entrapped inside a hydrogel or cross-linked to form a macroscopic network. Immobilized microgel matrices can provide unique properties and additional applications relative to bulk hydrogels or individual microgels alone. This article reviews manufacturing methods for producing biopolymeric microgels, and describes formation of microgel-based hydrogels via effective immobilization of microgels within a network.
... 10 Especially, the food proteins are potential oral delivery vehicles due to their good sensory attributes. 11 Water-soluble proteins such as gelatin and albumin have been widely explored as drug delivery carriers, but have limited ability to sustain drug release. 10 Zein is one of the few water-insoluble natural proteins with a high proportion (>50%) of hydrophobic amino acids (proline, alanine, and leucine). ...
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The study was aimed at systematically investigating the influence of shell composition on the particle size, stability, release, cell uptake, permeability and in-vivo gastrointestinal distribution of food protein-based nanocarriers for oral delivery applications. Three different core-shell nanocarriers were prepared using food-grade biopolymers including zein-casein (ZC) nanoparticles, zein-lactoferrin (ZLF) nanoparticles and zein-PEG (ZPEG) micelles. Nile red was used as a model hydrophobic dye for in-vitro studies. The nanocarriers had negative, positive and neutral charge respectively. All the three nanocarriers had a particle size of less than 200 nm and a low polydispersity index. The nanoparticles were stable at gastrointestinal pH (2-9) and ionic strength (10-200mM). The nanocarriers sustained the release of Nile red in simulated gastric and intestinal fluids. ZC nanoparticles showed the slowest release followed by ZLF nanoparticles and ZPEG micelles. The nanocarriers were taken up by endocytosis in Caco-2 cells. ZPEG micelles showed the highest cell uptake and transepithelial permeability followed by ZLF and ZC nanoparticles. ZPEG micelles also showed P-gp inhibitory activity. All the three nanocarriers showed bioadhesive properties. Cy 5.5, a near IR dye was used to study the in-vivo biodistribution of the nanocarriers. The nanocarriers showed longer retention in the rat gastrointestinal tract compared to the free dye. Among the three formulations, ZC nanoparticles was retained the longest in the rat gastrointestinal tract (≥24 hours). Overall, the outcomes from this study demonstrate the structure-function relationship of core-shell protein nanocarriers. The findings from this study can be used to develop food protein based oral drug delivery systems with specific functional attributes.