Title of article :
Bilirubin recognition via molecularly imprinted supermacroporous cryogels
Author/Authors :
Müge and Baydemir، نويسنده , , Gِzde and Bereli، نويسنده , , Nilay and Andaç، نويسنده , , Müge and Say، نويسنده , , Ridvan and Galaev، نويسنده , , Igor Yu and Denizli، نويسنده , , Adil، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2009
Pages :
6
From page :
33
To page :
38
Abstract :
Recent years molecular imprinting has received considerable attention as an excellent and simple approach to recognize small molecules and bioactive substances. The aim of this study is to prepare the bilirubin-imprinted supermacroporous cryogels which can be used for the adsorption of bilirubin from human plasma. N-methacryloyl-(l)-tyrosinemethylester (MAT) was chosen as the pre-organization monomer. In the first step, bilirubin was complexed with MAT and the bilirubin-imprinted poly(hydroxyethyl methacrylate-N-methacryloyl-(l)-tyrosine methylester) [BR-MIP] cryogel was produced by free radical polymerization initiated by N,N,N′,N′-tetramethylene diamine (TEMED) and ammonium persulfate (APS) pair in an ice bath. After that, the template molecules (i.e., bilirubin) were removed from the polymeric structure using sodium carbonate and sodium hydroxide. The maximum bilirubin adsorption amount was 3.6 mg/g polymer. The relative selectivity coefficients of the BR-MIP cryogel for bilirubin/cholesterol and bilirubin/testosterone mixtures were 7.3 and 3.2 times greater than non-imprinted poly(HEMA-MAT) [NIP] cryogel, respectively. The BR-MIP cryogel could be used many times without decreasing bilirubin adsorption amount significantly. Therefore, as a reusable carrier possessing high selectivity, BR-MIP cryogel has a potential candidate as a clinical hemoperfusion material.
Keywords :
Molecular recognition , molecular imprinting , Bilirubin , Affinity binding , Cryogels
Journal title :
Colloids and Surfaces B Biointerfaces
Serial Year :
2009
Journal title :
Colloids and Surfaces B Biointerfaces
Record number :
1969645
Link To Document :
بازگشت