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Lecture Encapsulation

Apr 05, 2018

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    Encapsulation

    technology

    Selected Topics in Food Technology

    Batrice Conde-Petit

    November 29, 2007

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    Encapsulation of food ingredients oradditives

    Mask unpleasant flavor

    Controlled release at the right place in the right time

    Increase solubility and/or bioavailability Protection of ingredient

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    Overview

    Microencapsulation by spray drying

    Encapsulation by extrusion Fluidized bed encapsulation

    Encapsulation by complex coacervation

    Encapsulation in self-assembled lipid structures Molecular encapsulation with cyclodextrins and starch

    Paper: Microencapsulation of probiotics for industrialapplications

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    Microencapsulation by spray drying

    Shell materials: gum accacia, maltodextrins,

    modified starch, whey proteins, ..

    For instance: hydrophobically modified starch

    (Octenyl substituted starch) for encapsulation offlavor oils

    Aqueous two phase system (ATPS) spraydrying for microorganism encapsulation

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    Octenyl succinicanhydride starch (OSA starch)

    S d i f h b d

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    Spray drying of an aqueos two-phase system based onpolyvinylpyrrolidon and dextran for encapsulation of biological

    material

    Enterococcus

    faecium M74

    (Millqvist et al 2000)

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    10 m

    Spray dried particles

    Partitioning of E. faecium

    in the dextran phase

    (Millqvist et al 2000)

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    Encapsulation by extrusion

    Mainly for encapsulation of volatiles in glassy carbohydrate matrices

    Long shelf life (up to 5 years) compared to spray drying (~ 1 year)

    Rather large particles (500 to 1000 m)

    Low load with simple carbohydrates (~ 10 %)

    e.g. Locked-in flavors, citric oils in glassy sucrose-glucose-glycerin matrix

    High load with hydrophobically modified starch (50 %)

    e.g. hydrophobically modified starch (octenyl substituted starch) forencapsulation of up to 50 % flavor oils

    Aqueous two phase system (ATPS) spray drying for microorganism

    encapsulation

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    Fluidized bed encapsulation

    Application of a uniform layer of shell material onto solidparticles (coating)

    Shell material: polysaccharides, proteins, emulsifiers,fats

    Examples: citric and ascorbic acid

    leavening agents

    Hotmelt fluidized bed coating: wax or fat as shellmaterial, coating at temperatures above the melting pointthe the shell material (40 to 80C)

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    Encapsulation by complex coacervation

    Based on associative phase behavior of a polymer blend

    Cationic and anionic water-soluble polymers interact in water andform a dense polymer-rich phase called a complex coacervate.

    In general coacervation is induced by a pH change to induce theformation of a dense polymer-rich phase that becomes the wallmaterial. The coacervates are usually stabilized by thermal

    treatment

    The dense coacervate phase wraps as a uniform layer aroundsuspended core materials such as an oily phase

    A widely applied polymer combination is gelatin and accacia gum

    Advantage: high load achievable (up to 99 %) and controlled

    release posssibilities

    Disadadvantage: high cost

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    Complex coacervation technology

    Formation of an oil-in-water emulsion

    Formation of the coating Stabilization of the coating

    Applications for:

    FlavorsFragrancesVitaminsBacteria and cells

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    B: Primary layer: complexation betweenoppositely charged polymer andsurfactant

    A: Secondary layer: complexationbetween the polyelectrolytes

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    Alginate beads

    alginate solution

    gelation ofalginate inCaCl2 bath

    washing step

    alginate beads

    Simple technique Mild process Applicable for almost any ingredient Widley applied for encapsulation of biomaterial

    www.nisco.ch

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    Liposome entrapment

    Application in cheese Proteases for cheese ripening Lysozyme for control of bacteria

    that produce butyric acid

    Shematic diagram of a sheet of lipid layer (A)and the liposome formed from the lipids (B)

    (Gibbs at al 1999)

    Encapsulation in self assembled

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    Encapsulation in self-assembledmonoglyceride structures

    Binary phase diagram ofsaturated monoglycerides in water

    Possible localization of guestmolecules within the invertedbicontinuous cubic phase

    1 hydrophylic2 amphiphilic

    3 lipophilic

    (Sagalowicz et al 2006)

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    Encapsulation in cyclodextrins

    Model of cyclodextrin

    Inclusion complexwww.uni-saarland.de

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    Amylose-ligand complexes as molecularencapsulation principle

    (Model fromGaillard 1987)

    Amylose-lipid complexesexist in cereal starches

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    Molecular encapsulation of unsaturatedfatty acidy

    Oxygen consumption to assess

    oxidative stability

    Free fatty acid

    Fatty acid in nanocapsule

    (Lalush et al 2005)

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    Lipids

    Fatty acids

    Emulsifiers

    - Monoglycerides

    - Lysolecithine

    Unsaturated fatty acids

    Volatile flavor compounds

    Alcohols & aldehydes

    Terpenes

    Lactones

    Decanal

    Complexing ligandsfor amylose

    Characterization of starch inclusion complexes

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    Characterization of starch inclusion complexes

    Wide-angle X-ray diffraction

    5 10 15 20 25 30Scattering angle 2 [degrees]

    Relative

    intensity

    DSC

    20 40 60 80 100 120 140 160

    Tem perature [C]

    121 C

    105 C

    Menthol

    Menthone

    2nd run

    1st run

    rmicheatflow

    End

    othermicheatflow

    Menthone

    Computer modeling

    FenchoneFenchone

    (Nuessli, Sigg, Conde-Petit, Escher 1999,Nuessli & Tran 1999)

    The complexation of starch has an influence on the

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    The complexation of starch has an influence on thecolloidal behaviour of starch

    Network

    25 m Spherulites

    Highcomplexation

    rates

    Lowcomplexationrates

    Gelation

    Bulk phase separation

    How does starch-flavor complexation influence

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    How does starch flavor complexation influenceflavor release?

    Extent of complexation

    (Heinemann C., Zinsli M., Dzik D., Graf S., Escher F., Conde-Petit B., 2003; Tietz, Buettner, Conde-Petit, 2007)

    Water

    Water

    Starch

    Starch

    Proton Transfer Reaction Mass spectrometry

    0.33 mg menthoneper g starch (db)

    4 % tapiocastarch dispersion

    48 mg menthone

    per g starch (db)

    2 % potatostarch dispersion

    Purge and trap (24 h) followed by GC

    Fl l i b h li i

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    Flavor encapsulation by spheruliticcrystallization of amylose-flavor complexes

    (Model from Kalinka and Hinrichsen, 1997)

    10 m

    Amylose--dodecalactoneSpherulites

    R f

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    References

    Gouin S., Microencapsulation: industrial appraisal of existing technologies andtrends, Tends in Food Science and Technology 15, 330-347 (2004).

    Millqvist-Fuerby A., Malmsten M., Bergenstahl B., An aqueous polymer two-

    phase system as carrier in the spray drying of biological material, J. of Colloidand Interface Science 225, 54-61 (2000).

    Jozwiakowski M., Jones D.M., Franz R.M., Characterization of a hot melt-fluidbed coating process for fine granuels, Pharmaceutical Research, 7 1119-1126(1990).

    Walstra P., Physical chemistry of foods, Marcel Dekker, New York (USA), 2003

    Sagalowicz L., Leser M.E., Watzke H.J., Michel M., Monoglyceride self-assemblystructures as delivery systems, Trends in Food Science and Technology 17, 204-

    214 (2006).

    Gibbs B., Kermasha S., Alli I., Mulligan C.N., Encapsulation in the food industry:a review, International Journal of Food Sciences and Nutrition 50, 213-224(1999).