The purposes of this research were to form chitosan oligosaccharide (CSO)/A2
β-casein nano-delivery systems (NDSs) and to investigate the effects of
production variables, such as CSO concentration levels (0.1%,
0.2%, and 0.3%, w/v) and manufacturing temperature (5°C,
20°C, and 35°C), on the production and physicochemical
characteristics of CSO/A2 β-casein NDSs to carry resveratrol. The
morphological characteristics of CSO/A2 β-casein NDSs were assessed by
the use of transmission electron microscopy (TEM) and particle size analyzer.
High-performance liquid chromatography (HPLC) was applied to determine the
entrapment efficiency (EE) of resveratrol. In the TEM images, globular-shaped
particles with a diameter from 126 to 266 nm were examined implying that NDSs
was successfully formed. As CSO concentration level was increased, the size and
zeta-potential values of NDSs were significantly (p<0.05) increased. An
increase in manufacturing temperature from 5°C to 35°C resulted in
a significant (p<0.05) increase in the size and polydispersity index of
NDSs. Over 85% of resveratrol was favorably entrapped in CSO/A2
β-casein NDSs. The entrapment efficiency (EE) of resveratrol was
significantly (p<0.05) enhanced with an increase in manufacturing
temperature while CSO concentration level did not significantly affect EE of
resveratrol. There were no significant (p<0.05) changes observed in the
size and polydispersity index of NDSs during heat treatments and storage in
model milk and yogurt indicating that CSO/A2 β-casein NDSs exhibited
excellent physical stability. In conclusion, the CSO concentration level and
manufacturing temperature were the crucial determinants affecting the
physicochemical characteristics of CSO/A2 β-casein NDSs containing
resveratrol.
Microencapsulation is a protective process for materials that are sensitive to
harsh conditions encounted during food manufacture and storage. The objectives
of this research were to manufacture a milk protein-based delivery system (MPDS)
containing
Lactobacillus rhamnosus
GG (LGG) using skim milk
powder and to investigate the effects of manufacturing variables, such as
reaction temerpature and holding time, on the physiccohemical properties of MPDS
and viability of LGG under dairy food processing and storage conditions. MPDS
was prepared using chymosin at varing reaction temperatures from 25°C to
40°C for 10 min and holding times from 5 to 30 min at 25°C. The
morphological and physicochemical properties of MPDS were evaluated using a
confocal laser scanning microscope and a particle size analyzer, respectively.
The number of viable cells were determined using the standard plate method.
Spherical-shaped MPDS particles were successfully manufactured. The particle
size of MPDS was increased with a decrease in reaction temperature and an
increase in holding time. As reaction temperature and holding time were
increased, the encapsulation efficiency of LGG in MPDS was increased. During
pasteurization, the use of MPDS resulted in an increase in the LGG viability.
The encapsulation of LGG in MPDS led to an increase in the viability of LGG in
simulated gastric fluid. In addition, the LGG viability was enhanced with an
increase in reaction temperature and holding time. In conclusions, the
encapsulation of LGG in MPDS could be an effective way of improving the
viability of LGG during pasturization process in various foods.
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