Citation:
Vladimir Chegel, Michael J. Whitcombe, Nicholas W. Turner, Sergey A. Piletsky, Deposition of functionalized polymer layers in surface plasmon resonance immunosensors by in-situ polymerization in the evanescent wave field, Biosensors and Bioelectronics, Volume 24, Issue 5, 1 January 2009, Pages 1270-1275. Selected Papers from the Tenth World Congress on Biosensors Shangai, China, May 14-16, 2008
Abstract:
Traditionally, the integration of sensing gel layers in surface plasmon
resonance (SPR) is achieved via “bulk” methods, such as precipitation, spin-
coating or in-situ polymerization onto the total surface of the sensor chip,
combined with covalent attachment of the antibody or receptor to the gel
surface. This is wasteful in terms of materials as the sensing only occurs at
the point of resonance interrogated by the laser. By isolating the sensing
materials (antibodies, enzymes, aptamers, polymers, MIPs, etc.) to this exact
spot a more efficient use of these recognition elements will be achieved. Here
we present a method for the in-situ formation of polymers, using the energy of
the evanescent wave field on the surface of an SPR device, specifically
localized at the point of interrogation. Using the photo-initiator couple of
methylene blue (sensitizing dye) and sodium p-toluenesulfinate (reducing agent)
we polymerized a mixture of N,N-methylene-bis-acrylamide and methacrylic acid in
water at the focal point of SPR. No polymerization was seen in solution or at
any other sites on the sensor surface. Varying parameters such as monomer
concentration and exposure time allowed precise control over the polymer
thickness (from 20–200 nm). Standard coupling with 1-ethyl-3-(3-
dimethylaminopropyl)carbodiimide and N-hydroxysuccinimide was used for the
immobilization of protein G which was used to bind IgG in a typical biosensor
format. This model system demonstrated the characteristic performance for this
type of immunosensor, validating our deposition m