Journal
ANALYTICA CHIMICA ACTA
Volume 625, Issue 1, Pages 110-115Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.aca.2008.07.010
Keywords
hydrogels; preparation pH; molecularly imprinting; hemoglobin; fibrinogen; myoglobin
Categories
Ask authors/readers for more resources
The hemoglobin-imprinted hydrogels were fabricated by using N-t-butylacrylamide (TBA) acrylamide (AAm) and itaconic acid (IA) monomers and hemoglobin (Hb, MW 65 kDa) imprinted molecule in pH buffer solutions (pH 4.0, 6.8 and 8.0). The nonimprinted hydrogels were also prepared at same conditions without Hb imprinting molecule. The effects of pH, initial concentration and adsorption time over the Hb adsorption capacity of both imprinted and nonimprinted hydrogels were analyzed and found to be strongly dependent on the preparation pH (pH(prep)). The maximum Hb adsorption for the imprinted hydrogel prepared at pH 4.0 was found to be 12.4 mg protein g(-1) dry gel in pH 4.0 buffer solution. This behavior was attributed to the formation of more accessible adsorption sites (imprints) because of the non-covalent interactions between the template and network during formation in pH 4.0 buffer solution which is below of the isoelectric point (pI 6.8) of Hb. Langmuir and Freundlich adsorption models were applied to describe the equilibrium isotherm. Langmuir analysis showed that an equal class of adsorption was formed in the hydrogels. Moreover, batch adsorption equilibrium and selectivity studies were also performed by using two reference molecules as fibrinogen (Fb, MW 340kDa) and myoglobin (Mb, MW 17kDa). The imprinted hydrogels have 1.5-2.2 times higher adsorption capacity for Hb than the nonimprinted hydrogels prepared at the same pHs, and also have 2.0-3.1 times higher selectivity for the imprinted molecule. (c) 2008 Elsevier B.V. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available