2005 APS March Meeting
Monday–Friday, March 21–25, 2005;
Los Angeles, CA
Session A4: Chemical and Biological Sensing with Microcantilevers
8:00 AM–11:00 AM,
Monday, March 21, 2005
LACC
Room: 515A
Sponsoring
Unit:
GIMS
Chair: A.T. Macrander, Argonne National Lab.
Abstract ID: BAPS.2005.MAR.A4.4
Abstract: A4.00004 : Diamond-based MEMS devices for biosensing based on electrochemical and gravimetric*
9:48 AM–10:24 AM
Preview Abstract
Abstract
Author:
John Carlisle
(Argonne National Laboratory)
Diamond offers several potential advantages as a platform material for
bioinorganic interfaces, including chemical and bio-inertness,
electrochemistry, and high acoustic velocity. Ultrananocrystalline diamond
(UNCD), with a unique combination of physical, chemical and electrical
properties, is attractive for a variety of biochemical/biomedical
applications such as hermetic bio-inert coatings, MEMS compatible
biosensors, and electrochemical biointerfaces. Over the past several years
we have worked on both the fundamental and applied science related to
enabling UNCD-based bioMEMS devices, which has encompassed both the
development of UNCD surface functionalization strategies that allow fine
control of surface hydrophobicity and bioactivity, as well as the
development of material integration strategies and surface micromachining
techniques to enable the microfabrication of UNCD structural layers (e.g.
cantilevers) that incorporate these functionalized surfaces into MEMS
devices which are back-end compatible with CMOS electronics. These devices
could thus combine the electrochemical and gravimetric transduction of the
selective adsorption of target analytes in MEMS structures fabricated
directly on top of a silicon microchip.. In the past year we have
successfully demonstrated the use of conducting UNCD thin films as
electrochemical biointerfaces, via the successful attachment of a redox
enzyme onto the UNCD surface, Glucose oxidase (GOD). The procedure to
achieve GOD immobilization involved the electrochemical immobilization of
nitrophenyl groups to the UNCD surface and transformation of nitrophenyl to
aminophenyl groups and the covalent bonding of GOD to the carboxyl groups
using the diisopropylcarbodiimide/ N-hydroxysuccinimide (DCC/NHS) as the
catalyst. After immobilization, the activity of the enzyme was demonstrated
via the direct electrochemical detection of hydrogen peroxide. We have also
developed CMOS-compatible UNCD MEMS cantilevers and fixed-fixed beam
structures, using both traditional photolithography and e-beam lithography
techniques.
*This work was supported by the US Department of Energy, BES-Materials Sciences, under Contract W-13-109-ENG-38; NSF/ONR under Contract N00014-89-J1178 (UNC-CH).
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2005.MAR.A4.4