scholarly journals Rheological Properties of Fish Gelatin Modified with Sodium Alginate

Polymers ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 743
Author(s):  
Svetlana R. Derkach ◽  
Daria S. Kolotova ◽  
Nikolay G. Voron’ko ◽  
Ekaterina D. Obluchinskaya ◽  
Alexander Ya. Malkin

Polyelectrolyte complexes of sodium alginate and gelatin obtained from cold-blooded fish were studied for potential application as structure-forming agents in food hydrogels. The mass ratio of sodium alginate to gelatin plays a decisive role in the sol-gel transition and rheological behavior of the complexes. Differences in the sol-gel transition temperature were observed upon heating and cooling, as is typical for such materials. We investigated the characteristics of this transition by measuring the isothermal changes in the elastic modulus over time at a constant frequency and the transition temperature at a range of frequencies. The kinetic nature of this transition depends on the composition of the complexes. A characteristic alginate-gelatin mass ratio is the ratio at which maximum transition temperature as well as elastic modulus and viscosity (rheological parameters) values are obtained; the characteristic mass ratio for these complexes was found to be 0.06. Calculation of the ionic group ratios in the biopolymers that form complexes and comparison of these data with the turbidimetric titration results clarified the origin of these maxima. Measuring the viscoelastic properties and the creep-elastic recoil of the samples allowed us to characterize these materials as viscoelastic media with a viscosity in the order of 103–104 Pa·s and an elastic modulus in the order of 102–103 Pa. These values drastically decrease at a certain stress threshold, which can be treated as the gel strength limit. Therefore, the observed rheological behavior of gels formed by fish gelatin modified with sodium alginate characterizes them as typical viscoelastic soft matter.

2015 ◽  
Vol 68 (10) ◽  
pp. 1593 ◽  
Author(s):  
Wenyao Zhen ◽  
Yannan Zhu ◽  
Weiping Wang ◽  
Zhaosheng Hou

In this paper, amphipathic poly(d,l-lactide-co-glycolide)-polyethylene glycol-poly(d,l-lactide-co-glycolide) (PLGA-PEG-PLGA) triblock copolymers were synthesized via bulk ring-opening polymerization with d,l-lactide (d,l-LA), glycolide (GA), and polyethylene glycol (PEG) as raw materials and tin(ii) bis(2-ethylhexanoate) (Sn(Oct)2) as catalyst. The synthesis and purification processes were free from organic solvent. The chemical structure of PLGA-PEG-PLGA was characterized by Fourier transform infrared spectroscopy, 1H NMR, gel permeation chromatography, differential scanning calorimetry, and thermo gravimetric analysis. The thermo-sensitivity of PLGA-PEG-PLGA aqueous solution was examined, and the results showed that the copolymers concentration, mass ratio of d,l-LA/GA, and molecular weight of PEG played important parts in controlling the sol–gel transition temperature. The sol–gel transition occurred at lower temperatures with higher copolymer concentrations and mass ratios of d,l-LA/GA. In contrast, the sol–gel transition temperature increased with higher molecular weights of PEG. In vitro drug release studies were carried out using ceftibuten as a model drug. The results indicated that PLGA-PEG-PLGA prepared with 30 wt-% PEG1500 and 70 wt-% PLGA (mass ratio of d,l-LA/GA = 2 : 1) was an effective system for achieving long-sustained controlled release. The drug release from the hydrogel showed a higher initial release followed by a slower pattern up to 120 h, and the mean retention time was ~50 h.


Cellulose ◽  
2014 ◽  
Vol 21 (5) ◽  
pp. 3737-3743 ◽  
Author(s):  
Yongbo Yao ◽  
Xiaolin Xia ◽  
Kanukai Susan Mukuze ◽  
Yumei Zhang ◽  
Huaping Wang

2020 ◽  
Vol 238 ◽  
pp. 116196 ◽  
Author(s):  
Fangyu Chen ◽  
Chao Chen ◽  
Dawei Zhao ◽  
Songping Zhang ◽  
Guanghui Ma ◽  
...  

2016 ◽  
Vol 101 (3) ◽  
pp. 1111-1120 ◽  
Author(s):  
Jung Hyun Kim ◽  
Eun Ju Yun ◽  
Nari Seo ◽  
Sora Yu ◽  
Dong Hyun Kim ◽  
...  

2017 ◽  
Vol 71 (3) ◽  
pp. 585-592 ◽  
Author(s):  
Johannes Schäfer ◽  
Ingrid Läufle ◽  
Christian Schmidt ◽  
Zeynep Atamer ◽  
Stefan Nöbel ◽  
...  

2008 ◽  
Vol 29 (6) ◽  
pp. 2036-2045 ◽  
Author(s):  
R. Medina-Esquivel ◽  
Y. Freile-Pelegrin ◽  
P. Quintana-Owen ◽  
J. M. Yáñez-Limón ◽  
J. J. Alvarado-Gil

1996 ◽  
Vol 12 (07) ◽  
pp. 604-608
Author(s):  
Zheng Hong-He ◽  
◽  
Zhang Qing-Zhi ◽  
Wang Jian-Ji ◽  
Wang Zheng-Yu ◽  
...  

2021 ◽  
Author(s):  
Xiaoxiao Li ◽  
Di Zhao ◽  
Kenneth J. Shea ◽  
Xueting Li ◽  
Xihua Lu

In this paper, soft thermosensitive photonic crystals are immobilized via a reversible temperature-triggered in situ sol–gel transition above their phase transition temperature (Tp), which may be a significant advance in the field.


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