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MICROENCAPSULATION IN THE
FOOD INDUSTRY
• PHYYSICAL METHOD
->SPRAY DRYING
->FLUIDZED BED DRYING
• CHEMICAL METHOD
->SOLVENT EXTRACTION METHOD
->CRYSTALLIZATION METHOD
To reduce the
To release the core To separate the
To protect the core evaporation rate of the To modify the nature To prevent unwanted
material slowly over components of the
material from core material to the of the original material flavor or taste of the
time at the constant mixture that would
degradation . surrounding for easier handling core material
rate react one another
environment
• The core material is the material over which
coating has to be applied to serve the specific
purpose. Core material may be in form of
Core solids or droplets of liquids and dispersions.
material • Pharmaceuticals: Drugs, probiotics, enzymes
• Food Industry: Vitamins, minerals, flavors, oils
• Agriculture: Pesticides, fertilizers, seeds
Physical methods
• Spray drying
• Spray chilling
• Fluidized bed coating
• Centrifugal co-extrusion
Chemical methods
• Solvent extraction
• Coacervation
• Crystallization
• Liposome entrapment
SPRAY DRYING
Spray drying is a widely used technique in the food industry for microencapsulation. It involves transforming a liquid feed
(containing the core material and wall material) into a dry powder by rapidly drying atomized droplets in a hot air stream. This
process creates tiny capsules (microcapsules) that enclose the core material within a protective wall material
Improved Stability: Microencapsulation protects sensitive ingredients Cost-Effective: Spray drying is often a continuous and efficient
from degradation by light, heat, moisture, or other environmental process, making it a cost-effective option for large-scale production.
factors, extending their shelf life and potency.
HOW DOES SPRAY DRYING FOR MICROENCAPSULATION
WORK?
Feed composition:
Process parameters: Wall material selection:
The properties of the core and
Atomization pressure, feed The chosen wall material
wall materials, their
flow rate, air temperature, and determines the release
concentration, and the solvent
flow rate significantly impact behavior, stability, and
used influence the drying
droplet size, drying time, and functionality of the
process and final microcapsule
microcapsule morphology. microcapsules
characteristics.
FLUIDIZED BED COATING FOR
MICROENCAPSULATION
Fluidized bed coating is another powerful technique for microencapsulation, particularly for coating existing solid
core materials like powders, crystals, granules, and pellets. In contrast to spray drying, which creates the
microcapsules from scratch, fluidized bed coating applies a thin film of wall material onto the pre-existing core
• The core material is loaded into aparticles.
container called a coater chamber
Preparation • Preheated air is passed through the chamber, creating an upward airflow. This airflow
suspends the particles in a fluidized state, making them behave like a boiling liquid
• The coating material, dissolved in a suitable solvent, is sprayed as a fine mist from a nozzle
Spraying positioned above the fluidized bed
• The mist droplets land on the individual particles, forming a thin film around them
• The hot air stream passing through the bed evaporates the solvent from the coating
Drying and material, solidifying the film and adhering it to the core particles.
evaporation
• The coated particles are then cooled before being discharged from the chamber. The final
Cooling and product is a dry powder containing individually coated microcapsules
collection
DIFFERENCE BTWEEN FLUIDIZED BED COATING AND SPRAY DRYING
• High purity: Selective extraction can isolate the desired bioactive compound from interfering
substances, enhancing its potency and efficacy.
• Concentration: Extraction concentrates the target compound, which can be advantageous for creating
microcapsules with sufficient loading of the active ingredient.
• Versatility: Various solvents and extraction techniques cater to a wide range of core materials and desired
properties.
• Solvent residues: Residual solvents need to be removed to acceptable levels for food safety and quality.
• Extraction efficiency: Choosing the right solvent and optimizing the extraction process are crucial for
maximizing target compound yield.
• Cost and scalability: Depending on the scale and complexity of the extraction process, the cost and feasibility
may vary.
CRYSTALLIZATION METHOD
CRYSTALLIZATION METHOD
Strong protection
Crystals are good shields against light, moisture, and other nasty things
Targeted delivery
Wall materials can be chosen to release the core under specific conditions like pH or
temperature
DIFFERENCE BTWEEN SOLVENT EXTRACTION AND CRYSTALLIZATION
Light: Light can break down vitamins and other sensitive compounds. The encapsulation
shield keeps them in the dark, preserving their potency and freshness. Think of it like
sunglasses for your food!
Oxygen: Oxygen can react with fats and oils, making them rancid. The encapsulation
wall blocks out oxygen, keeping your food tasting good longer. It's like a tiny airtight
container for your ingredients.
Building a
wall Moisture: Moisture can encourage mold and bacteria growth, spoiling your food. The
encapsulation shell acts as a waterproof raincoat, keeping your ingredients dry and
safe.
Heat: Some ingredients, like probiotics or certain flavors, can lose their effectiveness in high
temperatures. Encapsulation provides a heat-resistant shield, like a tiny oven mitt, ensuring
they stay potent even during processing or storage.
CONTD…
Ph-sensitive walls: these walls release their contents in the acidic environment of the
stomach, delivering nutrients or probiotics directly to their target zone. It's like a
microscopic delivery truck that drops off its cargo only at the right address.
Controlled
Release Swelling controlled release_in a system that regulates swelling, the active ingredient
cannot permeate the matrix. The fluid from the medium adsorbs onto the polymer
matrix when it is placed in a thermodynamically compatible media, causing the
polymer to swell and the active ingredient to diffuse into the swelled area
Osmotic pressure: the driving factor for the release of the active ingredient is the osmotic
pressure; creation of high osmotic pressure which result in release in the active component
APPLICATON IN FOOD INDUSTRY
MICROCAPSULE CONTAINING
MICROCAPSULE IN FOOD PRESERVATION
ANTIMICROBIAL
The most common types of preservatives that are encapsulated Eugenol and its derivatives are known to have antimicrobial
include polyphenols, which are flavonoids or tannins that have activity due to their light and temperature-sensitive properties
antioxidant activity and inhibit microbial growth and their insolubility and instability may limit their ability to
be incorporated in certain food matrices; however,
encapsulation may enhance their stability and usability,
allowing them to be used in a variety of meat produt
• Microencapsulation! Tiny capsules encase the omega-3s, protecting them from oxidation and masking
their fishy taste. These capsules are then incorporated into the yogurt, delivering a potent dose of omega-
Solut 3s without compromising the product's taste or texture.
ion
.
Benefits:
• Enhanced nutritional value: Yogurt fortified with microencapsulated omega-3s provides
consumers with a convenient and delicious way to boost their intake of these essential
nutrients.
• Improved flavor and shelf life: The capsules shield the omega-3s from oxidation, preventing
off-flavors and extending the yogurt's shelf life.
• Wider consumer appeal: Masking the fishy taste of omega-3s makes the yogurt more
palatable to a broader range of consumers.
Results:
• Studies have shown that microencapsulation can significantly increase the stability of
omega-3s in yogurt, preserving their health benefits.
• Consumer trials have demonstrated that yogurt fortified with microencapsulated omega-3s is
well-received, with no noticeable fishy taste or unpleasant texture.
CHALLENGES AND OPPORTUNITES
• Choosing the right wall material for capsules is crucial. It needs to be compatible with
Material Selection and the core material, food-grade, and offer desired release properties.
Design
• Finding the optimal balance between protection, permeability, and cost can be tricky.
Depending on the materials and intended use, encapsulated ingredients might require
Regulatory Hurdles
regulatory approval, adding complexity and potentially delaying market entry.
• This technology could enable the creation of highly customizable encapsulated structures
3D with specific shapes, sizes, and functionalities.
Printin • Custom-designed capsules could offer targeted release profiles, enhancing the efficacy of
g of nutrient delivery in food products
Encaps
ulated
Structu
res
As research and development continue to drive advancements in this field, the widespread
adoption of microencapsulation is expected to bring about profound changes, meeting the
dynamic needs and preferences of consumers while shaping the future of food production and
consumption.
REFERENCES
1. Agnikumar, S.; Manjusha, L.; Chouksey, M. K.; Tripathi, G.; Venkateshwarlu G. Delivery of Omega-3 Fatty Acids into
Cake through Emulsification of Fish Oil Milk and Encapsulation by Spray Drying with Added Polymer. Dry. Technol. 2015
2. Anjani K, Kailasapathy K, Phillips M. Microencapsulation of enzymes for potential application in acceleration of cheese
ripening. Int Dairy J 2007
4. Atmane, M.; Muriel, J.; Joel, S.; Stephane, D. Flavour Encapsulation and Controlled Release—A Review. Int. J. Food Sci.
Technol. 2006
5. Desai, K. G. H.; Park, H. J. Recent Developments in Microencapsulation of Food Ingredients. Dry. Technol. 2005
6. Hammad, U.; Hemlata, N.; Asif, M. T. M.; Sundara Moorthi, N. Microencapsulation: Process, Techniques and Applications.
Int. J. Res.Pharm. Biomed. Sci. 2011
7. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8912024/
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