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Emulsions as delivery systems: Flavors, nutrients, and phytochemicals John Coupland Penn State

Emulsions as delivery systems

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My presentation at the IFT 2011 meeting. Talking about how we can use emulsions to encapsulate stuff

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Page 1: Emulsions as delivery systems

Emulsions as delivery systems: Flavors, nutrients, and phytochemicals

John CouplandPenn State

Page 2: Emulsions as delivery systems

LimoneneGallic acid

Eugenol CarvacrolLog P=3.25, sol: 1.25 g/l

Log P=4.57, sol: 0.001 g/l

Log P=2.27, sol: 4.52 g/l

Vitamin D3Log P=8

Page 3: Emulsions as delivery systems

Aqueous Solubility

Carvacrol added

Aque

ous

cavr

acol 1.25 g/l

Page 4: Emulsions as delivery systems

Mass Transfer

Food

Page 5: Emulsions as delivery systems

Mass Transfer

Food

Page 6: Emulsions as delivery systems

• P = concentration in octanol (lipid)concentration in water

0 10 20 30 40 50 60 70 80 90 1000

0.20.40.60.8

11.21.4

Carvracrol added

Aque

ous

cavr

acro

l

zero fat

1% fat

Page 7: Emulsions as delivery systems

Emulsions as Delivery Systems

Page 8: Emulsions as delivery systems

Controlling Reactivity in Emulsions

Fig. 1. The impact of pH on the surface charge of whey protein isolate (WPI) stabilized salmon oil-in-water emulsions (A) and the differences in lipid oxidation rates (as measured by headspace propanal when the emulsion droplet is positively (pH 3 and 4) versus negatively (pH 6 and 7) charged) (B). Adapted by Hu et al., 2003. Figure reprinted from Warharo, McClements and Decker 2011

Page 9: Emulsions as delivery systems

Controlling Availability?

Inside droplet Outside droplet

~nm

Page 10: Emulsions as delivery systems

Solid Lipid Nanoparticles

Modified from: Visualizing the Structure of Triglyceride Nanoparticles in Different Crystal ModificationsHeike Bunjes, Frank Steiniger, and Walter RichterLangmuir 2007, 23, 4005-4011

Cryoelectron micrograph of tristearin nanoparticles (stabilized with a mixture of hydrogenated soybean lecithin and the bile salt sodium glycocholate) in the b-modification (bars represent 100 nm).

Page 11: Emulsions as delivery systems

O

O

OH

O

O

OO

O

OH

O

O

O

O

O

OH

O

O

OO

O

OH

O

O

O

O

O

OH

O

O

OO

O

OH

O

O

O

O

O

OH

O

O

OO

O

OH

O

O

O

Long Spacings (001)

2L

Image courtesy of Alejandro Marangoni (Guelph)

Fat Crystallization

Page 12: Emulsions as delivery systems

Controlling Availability: Crystallization

0% 20% 40% 60% 80% 100%0

0.002

0.004

0.006

0.008

0.01

Solid Fat Content

Aque

ous

conc

10% o/w emulsion containing hydrophobic solute (log P=3)

Page 13: Emulsions as delivery systems

3460 3470 3480 3490 3500 3510 3520Magnetic field (G)

Raw signal

Simulated signal

Aqueous

Lipid

d~200 nmLiquid drops

Page 14: Emulsions as delivery systems

after 24 h simulated

d~200 nmSolid drops

after 5 h simulated

after 24 h real

after 5 h real

Page 15: Emulsions as delivery systems

• Carrier lipid crystallization can force solute molecules to surface → higher availability

Page 16: Emulsions as delivery systems

Liquid oil droplets and solid droplets (5 hr)

Solid droplets (24 hr)

Probe reduction kinetics

d~200 nm

Page 17: Emulsions as delivery systems

• Carrier lipid crystallization can force solute molecules to surface → higher availability

Page 18: Emulsions as delivery systems

Acknowledgements

• Mr. Umut Yucel• Dr. Ryan Elias

This project was supported by the Agriculture and Food Research Initiative Competitive Grant no. 2009-65503-05960 from the USDA’s National Institute of Food and Agriculture: Improving Food Quallity