Astaxanthin-loaded zein/calcium alginate composite microparticles: Characterization, molecular interaction and release kinetics in fatty food simulant system

LWT ◽  
2020 ◽  
Vol 134 ◽  
pp. 110146 ◽  
Author(s):  
Ru Song ◽  
Yu Qi ◽  
Zhe Jia ◽  
Xinyan Liu ◽  
Rongbian Wei
1988 ◽  
Vol 5 (sup001) ◽  
pp. 467-483 ◽  
Author(s):  
N. De Kruijf ◽  
M. A. H. Rijk
Keyword(s):  

2017 ◽  
Vol 12 ◽  
pp. 9-15 ◽  
Author(s):  
Qin-Bao Lin ◽  
Xi-Zhen Liang ◽  
Qi-Zhi Su ◽  
Li-Jun Shan ◽  
Zhi-Wei Wang

2005 ◽  
Vol 22 (9) ◽  
pp. 892-898 ◽  
Author(s):  
E. M. Munguía-López ◽  
S. Gerardo-Lugo ◽  
E. Peralta ◽  
S. Bolumen ◽  
H. Soto-Valdez

2009 ◽  
Vol 12 (1) ◽  
pp. 69 ◽  
Author(s):  
Magdy M. Elnashar ◽  
Mohamed A. Yassin ◽  
Abou El-Fetouh Abdel Moneim ◽  
Elsayed M. Abdel Bary

This work is focused on investigating the unexpected behavior for the release kinetics of brilliant blue (BB) encapsulated into calcium alginate beads. By increasing the alginate concentration from 1-3% (w/v), the release of BB over time was found to follow two different behaviors. For the first two hours, the order was 1% > 2% > 3%, after which it was as follow: 1% > 3% > 2%. The unanticipated increase in BB release using 3% (w/v) alginate beads after two hours over that of 2% (w/v) alginate was examined by the swelling and bursting tests. The results were showing clear evidences by data and image the unusual behavior of 3% (w/v) alginate beads at two hours of swelling. This unexpected behavior for the 3% (w/v) alginate beads might be due to the higher osmotic pressure inside the beads. Overall, 2% (w/v) calcium alginate beads were considered to be the optimum formulation showing an excellent carrier for targeting drugs to the intestine, where the swelling of the beads were 60 % in the acidic medium, it was 5000 % in the alkaline medium.


Author(s):  
Inal Bakhytkyzy ◽  
Kuanyshbek Musabekov

<p>In this work the results of immobilization of anti-TB drugs rifampicin and fluconazole in alginate hydrogels were presented. Release kinetics of rifampicin and fluconazole fromswollen and dried calcium alginate microparticles were studied. It was revealed that the release of the drug from the swollen microparticles is higher than from the dried ones. Also the release of rifampicin from alginate microparticles coated with chitosan layer was studied. It was investigated that the thicker the layer of chitosan is, the slower drug releases. Thus, for the chitosan coating thickness of 25 microns, 95-100% rifampicin diffuses from the microparticles for 600-720 min. When using alginate-coated particles with a thickness of 65 microns and 125, during this time interval 60-70% drug released, respectively.</p>


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