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encapsulation of proteins

Jun 02, 2018

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    ENCAPSULATION OF PROTEIN

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    ENCAPSULATION OF PROTEIN

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    GROUP 4:

    Maha Saeed 2010-ag-2854 Izza Munir 2010-ag-2853

    Rakia Sahar 2010-ag-2855

    Faryal Farooq 2010-ag-2858

    Zunaira Saleem

    Tayyba Batool

    Rakhshnda

    Hafiz Wohaib

    M shoaib

    Kashif

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    ENCAPSULATION TECHNOLOGY Encapsulation can be defined as a process where a

    continuous thin coating is formed around solid particles,

    liquid droplets, or gas cells that are fully contained withinthe capsule wall.

    Encapsulation technology has been used in the food industry

    for more than 60 years as a way to provide liquid and solid

    ingredients as an effective barrier for environmental and/or

    chemical interactions until release is desired.

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    TYPE OF CAPSULE BY THEIR SIZE

    Encapsulated particles are called microcapsuleswhen the size range is between 0.2 and 5,000m.

    Macro capsules when the range is larger than

    5,000m.

    Nano capsules when the range is smaller than

    0.2m (200 nm).

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    CRITERIA TO BE AWARE Microcapsule properties may be changed to suit specific

    core applications, including composition , mechanism of

    release, particle size, final physical form, and cost.

    When designing encapsulation processes, it must be clearly

    established what type of functions encapsulated core can

    provide to the final product in order to select the most

    suitable coating material.

    Furthermore, the different processing conditions that the

    product will go through before release are of essential

    consideration.

    Other important features to take into account are the optimum

    concentration of the active core, the mechanism of release ,

    the final particle size, density, and stability requirements ofthe encapsulated ingredient. 5

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    MICRO-ENCAPSULATION OF

    PROTEIN

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    THE MICROENCAPSULATION

    TECHNIQUES APPLIED TO PROTEINS

    The two techniques mainly used for microencapsulation ofactive material by vegetable proteins are

    spray-drying

    Coacervation

    Both processes share the aspect of "green chemistry.

    Spray drying Spray-drying is a continuous process to convert an initial

    liquid into a solid powder of micro particles .

    It is a very common dehydration process used to form acontinuous matrix surrounding the active substances.

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    SPRAY DRYING CONTI..

    The initial liquid (solution, emulsion or suspension)

    containing wall and core materials is sprayed into a streamof heated air.

    The solvent, almost always water, is evaporated to give

    instantaneous powder production.

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    Advantages of spray drying:

    simple

    Inexpensive

    Rapid

    Disadvantages of spray drying

    loss of a significant amount of product

    possibility of degradation of sensitive products at high

    drying temperatures.

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    MICROENCAPSULATION BYCOACERVATION

    Microencapsulation by coacervation is carried out byprecipitation of wall forming materials.

    And it depends upon following fcators:

    change of pH or temperature,

    addition of a non-solvent or electrolyte compound

    This controlled desolvation results in the formation of a

    polymeric network around the core. This shell of coacervates can be solidified using a chemical

    or enzymatic cross-linker.

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    Simple Coacervation:

    Simple coacervation involves only one colloidal solute and

    thus formation of a single polymer envelope.

    Complex Coacervation:

    Complex coacervation is produced by mixing two oppositelycharged polyelectrolytes for shell formation around an active

    core.

    These two processes give high values (up to 100%) of

    microencapsulation efficiency (MEE).

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    PLANT PROTEINS IN MICROENCAPSULATION

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    PLANT PROTEINS IN

    MICROENCAPSULATION Used as wall forming material for variety of active

    compounds

    Potentially useful microencapsulation proteins are from

    Pea

    Soya

    Wheat

    Rice

    Oat

    Barley

    Corn

    Sunflower

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    Pea protein Protein content 20-30%

    Protein fractions: Globulin 65-80%, Albumin & Glutelin

    Have good gel forming & emulsifying properties

    Polysaccharide-protein interactions give excellent functional propertieswithout chemical & enzyme treatment.

    This interaction creates stable emulsion, better particle size distribution

    & improved efficiency of microencapsulation.

    Used for active materials protection & emulsion stabilization

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    MICROENCAPSULATION WITH PEA

    PROTEIN AND POLYSACCHARIDE AS

    WALL MATERIAL

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    SOYA PROTEIN Protein fractions: Glycenin 35-40%, Conglycin 50-90%

    Have interesting gel forming, emulsifying & surfactantproperties

    Used as individual coating material or mixed with

    polysaccharides.

    Protein & carbohydrate as carrier material favors better

    protection, oxidative stability & drying properties.

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    MICROENCAPSULATION WITH SPI BASED

    WALL MATERIAL

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    WHEAT PROTEIN

    Gluten important protein fraction

    Other proteins are glutenin and gliadin

    Used for gel & film formation due to viscoelasticity & low

    solubility

    Wheat-polysaccharide interactions give goodencapsulation to surface active materials

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    RICE PROTEIN Protein content 12-20% in whole rice

    In white rice 6-15%

    Protein fractions: Glutenin 75%, Globulin 15%, Albumin6%, Prolamin 3%

    Show excellent foaming and emulsifying properties Make bonds with polysaccharides(alginate &

    carrageenan)

    These properties provide favorable characteristics for wallformation.

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    OAT PROTEIN

    Protein content 12-24%

    Have very attractive amino acid composition

    Protein fractions: Globulin 70-80%, Albumin 20-30%

    Have poor solubility & functional properties

    Solubility, emulsifying & foaming capacity can be

    improved by hydrolysis, acetylation & succinylation

    Native properties are not suitable for encapsulation.

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    BARLEY PROTEIN

    Protein fractions: Glutelin, Hordein

    Both fractions show excellent film forming & emulsifyingproperties.

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    CORN PROTEIN

    Protein fractions: Prolamin, Zein

    Soluble in hydro-alcoholic solution

    Well known for filmogenic properties.

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    Cereal proteins in

    microencapsulation

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    SUNFLOWER PROTEIN

    27% protein content in defatted sunflower flour

    20-40% crude protein in dehulled seed

    Protein fractions: Globulin 55-60%, Albumin 17-23%, Glutelin11-17%, Prolamin1-4%

    Better emulsifying properties at pH 7-8 Heating increases emulsion stability but reduces emulsion

    formation capacity

    Solubility of globulin depends on pH

    Albumin has good solubility independent of pH Less efficient in foaming but foams are more stable overtime

    Properties improvement by chemical treatment

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    INDUSTRIAL APPLICATIONS OF

    MICROENCAPSULATION BYVEGETABLE PROTEINS

    Pea proteins show good properties for theirapplication, in particular for the production of

    Adhesives

    Bioplastics

    Emulsifiers

    Wall forming materials

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    Functional properties of wheat proteins and corn zein

    have several applications in the field of

    Adhesives.

    Matrix materials for microencapsulation.

    Textiles

    Cosmetics. Biodegradable plastics.

    Soy bean proteins are used as

    wall forming materials in the food industry to mask the

    undesirable taste of some nutritional additives.

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    CONCLUSIONS AND FUTURE

    PROSPECTS

    The various studies have proved the ability of proteins to

    efficiently protect different forms of active materials(hydrophilic or hydrophobic, solid or liquid) as an

    encapsulating agent, using both spray-drying and

    coacervation methods.

    Vegetable proteins widely used as encapsulants are pea

    protein isolate, soy protein isolate, wheat gliadins, corn

    zein and barley protein.

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    REFERENCES:

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    Alla Nesterenko1,2, Isabelle Alric1,2, Francoise

    Silvestre1,2, Vanessa Durrieu1,21 Universit de Toulouse,INP-ENSIACET, LCA (Laboratoire de Chimie Agro-

    industrielle), F-31030 Toulouse,France 2 INRA, UMR

    1010 CAI, F-31030 Toulouse, France.

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