application of alternative food-preservation - Bentham Science
application of alternative food-preservation - Bentham Science
application of alternative food-preservation - Bentham Science
You also want an ePaper? Increase the reach of your titles
YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.
190 Application <strong>of</strong> Alternative Food-Preservation Technologies Gallo and Corbo<br />
Chemical Methods<br />
Emulsion Polymerization<br />
In this method a water-insoluble monomer is added dropwise into the aqueous polymerization medium,<br />
containing the ingredient to be encapsulated and a emulsifier. Initially, polymer molecules form primary nucleus,<br />
thus they growing and entrapping the core material [2].<br />
The size <strong>of</strong> the particles is ca. 50-500 μm [3].<br />
Interfacial Polymerization<br />
In this technology, the polycondensation <strong>of</strong> two complementary monomers takes place at the interface <strong>of</strong> two<br />
immiscible phases, that are mixed under carefully-controlled conditions to form small droplets <strong>of</strong> one phase in<br />
the other. For this process is it necessary to use a small amount <strong>of</strong> a suitable stabilizer to prevent droplet<br />
coalescence or particle coagulation. Microcapsules can be either monocore or matrix type, depending on the<br />
solubility <strong>of</strong> the polycondensate in the droplet phase [2].<br />
This method was initially applied for the preparation <strong>of</strong> semipermeable artificial cells and then used for many<br />
materials: solids, aqueous solution and organic liquids. The size <strong>of</strong> microcapsules varies from 2 to 6 µm to 2000<br />
µm [3].<br />
In-situ Polymerization<br />
The process involves the direct polymerization <strong>of</strong> a single monomer shell carried out on a core materials surface.<br />
Coating thickness is <strong>of</strong> 0.2-75 µm and the coating is uniform [4].<br />
Coacervation<br />
It is the most promising microencapsulation technology, because the recovery is up to 99%; this method is used<br />
mainly to encapsulate flavour oil, fish oil, vitamins and enzymes [5].<br />
This technique is carried out by preparing an aqueous polymer solution (1-10%) containing the core material at<br />
40-50°C; a suitable stabilizer can be added to the mixture to maintain the individuality <strong>of</strong> the microcapsules. A<br />
coacervating agent is gradually added to the solution, thus leading to the formation <strong>of</strong> partially desolvated<br />
polymer molecules, and hence their precipitation on the surface <strong>of</strong> the core particles. The coacervation mixture is<br />
cooled to about 5-20°C, followed by the addition <strong>of</strong> a crosslinking agent to solidify the microcapsule wall<br />
formed around the core particles [2].<br />
The most studied and well understood coacervation system is probably the gelatin/gum acacia system, which<br />
presents a major drawback, due to the use <strong>of</strong> gelatin in <strong>food</strong>s. However, this issue could be solved by using an<br />
enzymatic crosslinking [5].<br />
Liposome<br />
Developed in recent years, nowadays this technology is used routinely in <strong>food</strong> industry and in pharmaceutical<br />
area, due to: the high encapsulation efficiency, the simple production method and the good stability <strong>of</strong><br />
capsules [5].<br />
Liposomes or phospholipide vesicles are structures composed <strong>of</strong> a lipid vesicle bilayers and are generally large,<br />
irregular and unilamellar. Chemically, liposome is an amphoteric compound containing both positive and<br />
negative charges [6].<br />
Today, the methods for liposome formation do not use the sonication or organic solvent, and allow the<br />
continuous production <strong>of</strong> microcapsules on a large scale. Several authors have proposed different methods for<br />
liposome production for microencapsulation technology [5].<br />
The maximum particle size (16 μm) is obtained by using a liposome concentration <strong>of</strong> 4 g/l [6].