2013
DOI: 10.1016/j.seppur.2013.08.026
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Immunoglobulin G purification from bovine serum with pseudo-specific supermacroporous cryogels

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Cited by 41 publications
(26 citation statements)
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“…Third, particles embedding into a cryogel network caused an increase in the specific surface area, which is one of the most efficient parameters on the adsorption capacity. 4,41,42 Finally, the combination of these features formed a synergy to get higher adsorption capacities with fast and efficient adsorption kinetics.…”
Section: Methodsmentioning
confidence: 99%
“…Third, particles embedding into a cryogel network caused an increase in the specific surface area, which is one of the most efficient parameters on the adsorption capacity. 4,41,42 Finally, the combination of these features formed a synergy to get higher adsorption capacities with fast and efficient adsorption kinetics.…”
Section: Methodsmentioning
confidence: 99%
“…The reagents acrylamide (AAm) and 2‐hydroxyethyl methacrylate (HEMA) were used as the precursor of the affinity cryogel because of their neutrality and inert nature, which minimized nonspecific interactions with proteins. By controlling the freezing temperature and the precursor concentration, the pore size of cryogels was in the range of 50‐200 µm [45,46], which was not large enough for the purification from a viscous solution. Formation of cryogels with larger pore sizes by decreasing the concentration of the monomer requires a sacrifice in the cryogel mechanical strength, which cannot be applied in practice.…”
Section: Introductionmentioning
confidence: 99%
“…The adsorption kinetics experiments were carried out in duplicate at room temperature as described in Daoud‐Attieh et al (). The C10/10 column (GE Healthcare, USA) packed with 1.0 mL of P‐Tyr‐agarose was equilibrated with NaP 10 mmol L −1 , pH 6.0 (adsorption buffer) at 1.0 mL min −1 (superficial velocity of 76.4 cm h −1 ).…”
Section: Methodsmentioning
confidence: 99%
“…The pseudo‐first‐order and pseudo‐second‐order kinetic models were applied to the experimental data on the adsorption kinetics of human IgG using the following equations (Daoud‐Attieh et al, ; Oliveira et al, ): qt=qe()1+ek1t qt=k2qe2t1+tk2qnormale in which q e and q t are the amount of IgG adsorbed (mg) onto P‐Tyr‐agarose (g) at equilibrium and time t (min), respectively; k 1 (min −1 ) is the rate constant for the pseudo‐first‐order adsorption kinetics and k 2 (g mg −1 min −1 ) is the rate constant for the pseudo‐second‐order kinetics.…”
Section: Methodsmentioning
confidence: 99%