Production of surface plasmon resonance based assay kit for hepatitis diagnosis


UZUN L., Say R., ÜNAL S., DENİZLİ A.

BIOSENSORS & BIOELECTRONICS, vol.24, no.9, pp.2878-2884, 2009 (Peer-Reviewed Journal) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 24 Issue: 9
  • Publication Date: 2009
  • Doi Number: 10.1016/j.bios.2009.02.021
  • Journal Name: BIOSENSORS & BIOELECTRONICS
  • Journal Indexes: Science Citation Index Expanded, Scopus
  • Page Numbers: pp.2878-2884
  • Keywords: Molecular imprinted polymers, Diagnostic kits, Hepatitis B, Surface plasmon resonance, MOLECULARLY IMPRINTED POLYMERS, REAL-TIME, SUPERMACROPOROUS CRYOGELS, SYNTHETIC RECEPTOR, ANTIBODY MIMICS, LABEL-FREE, RECOGNITION, PROTEIN, SENSOR, DNA

Abstract

Hepatitis B surface antibody (HBsAb) imprinted poly(hydroxyethyl methacrylate-N-methacryloyl-L-tyrosine methyl ester) (PHEMAT) film on the surface plasmon resonance (SPR) sensor chip was prepared for diagnosis of HBsAb in human serum. Gold SPR chip surface was modified with allyl mercaptane and, then, HBsAb-imprinted PHEMAT film was formed on the chip surface. Surface characterization of the non-modified, allyl mercaptane modified and HBsAb-imprinted PHEMAT SPR chips were investigated with contact angle, atomic force microscopy (AFM). Kinetic studies were performed using HBsAb positive human serum. In order to determine the kinetic and binding constants, Scatchard, Langmuir, Freundlich and Langmuir-Freundlich models were applied to experimental data. Scatchard curve shows that HBsAb imprinted SPR chip has some surface heterogeneity, SPR chip obeyed the Langmuir adsorption model. The maximum detection limit was 208.2 mIU/mL K-A and K-D values are 0.015 mIU/mL and 66.0 mL/mIU, respectively. Control experiments of the SPR chip were performed using non-immunized, HBsAb negative serum. The control experiment results show that SPR chip does not give any noticeable response to HBsAb negative serum. (C) 2009 Elsevier B.V. All rights reserved.