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Gelation, alginates

Uses. Alginates are used in a wide range of appHcations, particularly in the food, industrial, and pharmaceutical fields (25—27). As shown in Table 5, these appHcations arise from the properties of gelation, thickening/water holding, emulsification, stabilization/binding, and film forming. [Pg.432]

Pectins are generally classed according to their ester content as high methoxyl pectins (>50% of the carboxyl groups esterified) or low methoxyl pectins (<50% of carboxyl groups esterified) (pectic acid, methyl ester [9049-34-1]). Low methoxyl pectins, like algins, require calcium for gelation. [Pg.435]

Fig. 5.5 (A) Alginate block copolymer structure with random sequences (B) divalent cations induced gelation of alginate (formation of egg-box structure). Fig. 5.5 (A) Alginate block copolymer structure with random sequences (B) divalent cations induced gelation of alginate (formation of egg-box structure).
Wet cells (5g) are suspended in 15 ml of a 1% sodium alginate solution. The mixture is then forced through a syringe needle into a 0.05 M CaCl2-solution containing the necessary nutrients for the cell. Gelation occurs almost immediately. [Pg.255]

Morris, E.R., Rees, D.A., Thom, D., Boyd, J. (1978). Chiroptical and stoichiometric evidence of a specific, primary dimerization process in alginate gelation. Carbohydrate Research, 66, 145-154. [Pg.227]

The principle took advantage of the gelation of alginate at room temperatures in the presence of calcium ions. Recently, a new method was described by Alleyene et al. [16] based on a microcube concept, and compared with older methods. [Pg.234]

Propyleneglycol alginates do not precipitate from acidic media and their acid stability increases in proportion to the propyleneglycol content. Additionally, those esters with DS > 60% are not precipitated by Ca2 +, because the bulky propyleneglycol substituent hinders the prerequisite alignment for gelation and precipitation. These esters are more tolerant of alcohol than the unesterified alginate. [Pg.175]

Toft, K., Grasdalen, H., and Smidsrod, O. (1986). Synergistic gelation of alginates and pectins. In Chemistry and Function of Pectins, ACS Symposium Series 310, pp. 117-132. Am. Chem. Soc., Washington, DC. [Pg.218]

Calcium alginate Gelation None stable in 0.1 N HC1, but not in simulated intestinal fluids ... [Pg.168]

Calcium alginate and poly-L-lysine Gelation Doxorubicin, oligonucleotides [28,89]... [Pg.168]


See other pages where Gelation, alginates is mentioned: [Pg.356]    [Pg.213]    [Pg.353]    [Pg.110]    [Pg.356]    [Pg.213]    [Pg.353]    [Pg.110]    [Pg.355]    [Pg.106]    [Pg.28]    [Pg.83]    [Pg.85]    [Pg.8]    [Pg.11]    [Pg.42]    [Pg.223]    [Pg.276]    [Pg.21]    [Pg.169]    [Pg.112]    [Pg.3]    [Pg.16]    [Pg.240]    [Pg.171]    [Pg.174]    [Pg.211]    [Pg.123]    [Pg.24]    [Pg.258]    [Pg.60]    [Pg.249]    [Pg.134]    [Pg.162]    [Pg.7]    [Pg.10]    [Pg.194]    [Pg.496]    [Pg.31]    [Pg.124]    [Pg.112]   
See also in sourсe #XX -- [ Pg.94 , Pg.95 , Pg.96 , Pg.101 ]




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Algin

Alginate

Alginate gelation

Alginate gelation

Alginate, ionotrope gelation

Alginate-pectin gelation

Alginic acid gelation

Gelation of alginate

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