International Journal of Applied And Pure Science and Agriculture CHITOSAN -WHEY PROTEIN COMPLEX (CS-WP) AS DELIVERY SYSTEMS TO IMPROVE BIOAVAILABILITY OF IRON
El-Sayed M. M.; Hassan, Zakaria Mohamed Rezk; Mervat I. Foda; Awad R. A.; Heba H. Salama;
Abstract
Use of whey proteins as a natural nano-capsular vehicle to carry and improve the bioavailability of
iron was investigated in this study. Nanoparticles of whey protein concentrate-chitosan (CS-WPC)
complex were prepared with the aim of developing a biocompatible carrier for the oral
administration of iron as a nutraceuticals. Effects of pH, concentration of native CS-WPC and iron
on the nanoparticles with sodium tripolyphosphate (TPP) prepared by ionic gelation were
investigated. CS-WPC were loading with different iron concentration namely; ferrous sulphate.
The surface charge of the particles was positive and negative that strongly pH dependent and
showed positive charge after iron loading at low protein concentration and was negative at 8 and 12
% when the pH increased to 5.5. The association efficiency (AE) and loading efficiency (LE) of CSWPC
nanoparticles was highly sensitive to formulation pH. This adsorption can be mainly
attributed to electrostatic, hydrophobic interactions and hydrogen bonding between WPC and CS.
The iron release experiments showed that the nanoparticles prepared with native WPC had
favorable properties to resist acid and pepsin degradation in simulated gastric conditions. When
transferred to simulated intestinal conditions, the WPC shells of the nanoparticles were not
degraded by pancreatin showing the same results with and without enzymes after 6 h. CS-WPC
iron nanoparticles at level 0, 3, 6, 9, 12 mg/g protein showed very high bioavailability after
evaluated in simulated gastric and intestinal fluids in the presence or absence of the enzymes.
iron was investigated in this study. Nanoparticles of whey protein concentrate-chitosan (CS-WPC)
complex were prepared with the aim of developing a biocompatible carrier for the oral
administration of iron as a nutraceuticals. Effects of pH, concentration of native CS-WPC and iron
on the nanoparticles with sodium tripolyphosphate (TPP) prepared by ionic gelation were
investigated. CS-WPC were loading with different iron concentration namely; ferrous sulphate.
The surface charge of the particles was positive and negative that strongly pH dependent and
showed positive charge after iron loading at low protein concentration and was negative at 8 and 12
% when the pH increased to 5.5. The association efficiency (AE) and loading efficiency (LE) of CSWPC
nanoparticles was highly sensitive to formulation pH. This adsorption can be mainly
attributed to electrostatic, hydrophobic interactions and hydrogen bonding between WPC and CS.
The iron release experiments showed that the nanoparticles prepared with native WPC had
favorable properties to resist acid and pepsin degradation in simulated gastric conditions. When
transferred to simulated intestinal conditions, the WPC shells of the nanoparticles were not
degraded by pancreatin showing the same results with and without enzymes after 6 h. CS-WPC
iron nanoparticles at level 0, 3, 6, 9, 12 mg/g protein showed very high bioavailability after
evaluated in simulated gastric and intestinal fluids in the presence or absence of the enzymes.
Other data
| Title | International Journal of Applied And Pure Science and Agriculture CHITOSAN -WHEY PROTEIN COMPLEX (CS-WP) AS DELIVERY SYSTEMS TO IMPROVE BIOAVAILABILITY OF IRON | Authors | El-Sayed M. M.; Hassan, Zakaria Mohamed Rezk ; Mervat I. Foda; Awad R. A.; Heba H. Salama | Keywords | Nanoparticles; Whey proteins concentrate; Chitosan; Iron bioavailability | Issue Date | Nov-2015 | Publisher | International Journal of Applied And Pure Science and Agriculture | Journal | International Journal of Applied And Pure Science and Agriculture | Start page | 34 | End page | 46 | DOI | ISSN: 2394-823X |
Attached Files
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| chitosan-whey-protein-complex-cs-wp-as-delivery-systems-to-improve-bioavailability-of-iron.pdf | 2.24 MB | Adobe PDF | Request a copy |
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