Encapsulation of herbal aqueous extract through absorption with ca-alginate hydrogel beads

2010 ◽  
Vol 88 (2-3) ◽  
pp. 195-201 ◽  
Author(s):  
Eng-Seng Chan ◽  
Zhi-Hui Yim ◽  
Soon-Hock Phan ◽  
Rachel Fran Mansa ◽  
Pogaku Ravindra
2004 ◽  
Vol 21 (5) ◽  
pp. 565-573 ◽  
Author(s):  
B. Doumèche ◽  
M. Küppers ◽  
S. Stapf ◽  
B. Blümich ◽  
W. Hartmeier ◽  
...  

2018 ◽  
Vol 7 (4.37) ◽  
pp. 53 ◽  
Author(s):  
Haneen Ahmed Khudhair ◽  
. .

Quinoline is a nitrogen heterocyclic compound (NHC) with a molecular formula of C9H7N. Microbial degradation of quinoline occurs under both aerobic and anaerobic conditions. In this study, the aerobic biodegradation of quinoline was investigated with activated sludge which was taken from a municipal sewage wastewater treatment plant in the air-lift bioreactor (ALBR).The activated sludge was entrapped in poly-vinyl-alcohol-calcium alginate (PVA-Ca alginate) hydrogel beads. The optimal conditions for microbial cells entrapment, such as Ca-alginate concentration, biomass concentration in the hydrogel bead and bead size, were determined with concerning to improve the quinoline degradation rate. Also, the initial quinoline concentration was determined. The optimum temperature and initial pH for quinoline degradation were 30°C and pH 7–8, respectively. During the biodegradation process, the culture broth became yellow and brown in turn, which indicated that several intermediates were generated. The results showed that the diversity of microbial cells improves and accelerates the quinoline biodegradation. The repeated use of the hydrogel beads for quinoline degradation was performed and the results revealed that the beads were active and intact up to 4 successive cycles without breakage or loss their stability in the continuous mode. Thus, (PVA-Ca alginate) hydrogel beads have great potential to be a matrix for the cell immobilization in quinoline biodegradation. The various initial concentrations of quinoline (50, 100, 250, and 500mg/L) were completely degraded in batch-mode experiments; under optimal conditions: PVA conc., 80%w/v; calcium alginate conc., 20%w/v; initial biomass concentration the hydrogel bead, 3mL / 10 mL of gel solution; and the hydrogel bead size, about 3mm in diameter, at different time intervals (4, 6, 10, and 14h), respectively.   


Lab on a Chip ◽  
2021 ◽  
Author(s):  
Husnain Ahmed ◽  
Bjørn Torger Stokke

Micron-sized alginate hydrogel beads are extensively employed as an encapsulation medium for biochemical and biomedical applications. Here we report on the microfluidic assisted fabrication of calcium alginate (Ca-alginate) beads by...


2017 ◽  
Vol 105 ◽  
pp. 924-930 ◽  
Author(s):  
Yang Li ◽  
Chao Feng ◽  
Jing Li ◽  
Yuzhi Mu ◽  
Ya Liu ◽  
...  

2021 ◽  
Author(s):  
Xiao Zhang ◽  
Zhiyue Li ◽  
Taoyi Zhang ◽  
Jing Chen ◽  
Wenxi Ji ◽  
...  

A novel zeolitic imidazolate framework-8 (ZIF-8) alginate composite hydrogel material (PVA/SA@ZIF-8) is alginate composite bead which was fabricated by grafting ZIF-8 on the surface of the sodium alginate hydrogel beads...


e-Polymers ◽  
2005 ◽  
Vol 5 (1) ◽  
Author(s):  
Piotr Woźniak ◽  
Marek Kozicki ◽  
Janusz M. Rosiak ◽  
Jacek Przybylski ◽  
Malgorzata Lewandowska-Szumieł

AbstractHuman cartilage derived cells were encapsulated in alginate hydrogel beads. Viability of the cells was determined using both qualitative (microscopy) and quantitative (MTT and NR assays) examination. Microscopy indicated that encapsulated cells remained viable during the 7-days experiment. The quantitative tests failed to give reliable results. Possible factors affecting the results of the quantitative study are discussed.


Author(s):  
MIZANURFAKHRI GHAZALI ◽  
SHARANIZA AB-RAHIM ◽  
MUDIANA MUHAMAD

Introduction: Human Norovirus (HuNoV), a food-borne virus is the leading cause for acute gastroenteritis. However, its inability to propagate in vitropersists as major challenge in understanding HuNoV biology.Objective: This study aims to determine an effective culture system for HuNoV.Methods: The Caco-2 cells were cocultured with Raji B cells on alginate hydrogel beads. Scanning electron microscopy (SEM) was performed to confirmthe three-dimensional (3D) cells morphology. Western blot (WB) analysis was performed to detect protein markers expressed by Microfold (M) cells.Results: Optimization of Caco-2 cells monoculture in the alginate hydrogel beads showed optimum number of cells of 1 × 106 cells/ml, indicatedby the intact structure of the beads. Result of SEM showed clear structure of monoculture in the alginate hydrogel beads indicated by the presenceof smooth and regular apical surface while the coculture showed reduced apical surface of M cells. The result of WB showed downregulation ofUlex europaeus antibody expression.Conclusion: It is evident that the expression of M cells grown in 3D alginate hydrogel beads was successful, indicated by the structural morphologyseen under SEM as well as expression of protein marker by M cells. This established in vitro system is highly potential for cultivation of HuNoV.


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