Adsorption of serum albumin and γ-globulin from single and binary mixture and characterization of pHEMA-based affinity membrane surface by contact angle measurements
Yükleniyor...
Tarih
2005
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Elsevier Science Bv
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
In this study, an affinity membrane was synthesized using 2-hydroxyethylmethacrylate (HEMA) via UV-initiated photopolymerization. A dye-ligand (i.e., Procion Red HE-3B; Red-120) was covalently immobilized onto membrane. Human serum albumin (HSA) and human gamma-globulin (HIgG) adsorption onto pHEMA-Red-120 membrane were studied using bare poly(hydroxyethylmethacrylate) (pHEMA) membrane as a control system. The information about surface energy, hydrophobicity and chemical heterogeneity of the affinity membrane was obtained by contact angle measurements. The contact angle values of the affinity membrane were determined by sessile drop method using water, glycerol and diiodomethane as test liquids. Component and parameters of the surface free energy of all the investigated samples were calculated from measured contact angle values using the acid-base method of the van Oss. The adsorption of HSA and HIgG significantly changed both the contact angles and component of surface free energies of the affinity membrane. The reversible HSA and HIgG adsorption on the pHEMA-Red-120 followed the Freundlich and Langmuir-Freundlich isotherm models. Selectivity of the affinity membrane was tested at different pH values to HSA and HIgG and the protein concentration of in the binary system was determined by HPLC. The affinity membrane was stable when subjected to sanitization with sodium hydroxide after repeated adsorption-elution cycles. (c) 2005 Elsevier B.V. All rights reserved.
Açıklama
Anahtar Kelimeler
microporous membrane, affinity chromatography, dye-ligand, adsorption, separation, albumin, gamma-globulins, contact angle
Kaynak
Biochemical Engineering Journal
WoS Q Değeri
Q1
Scopus Q Değeri
Q2
Cilt
26
Sayı
1
Künye
closedAccess
