
Professor
Jonathan G. Shackman's Research Interests

Recent
developments in microfabrication technologies
have opened up many possible avenues for revolutionary
research in a wide range of fields and have found
wide spread application in the chemical and biological
sciences. Miniaturization strategies frequently
seek to encapsulate all processes of analysis,
including sample preparation, separations, detection,
and data analysis. Capillary electrophoresis
(CE) is a powerful analytical tool that is commonly
utilized in these microfluidic devices to perform
the separation of analytes. While affording
rapid, high resolution separations with small
sample requirements, CE suffers from low concentration
limits of detection (LOD) when using the most
common optical detection techniques ( i.e.
, absorbance and fluorescence). The
detection problem has been exacerbated when translated
from fused silica capillaries to microdevices,
which frequently employ thick borosilicate glass
or polymeric materials, as well as extremely small
channel dimensions, that further degrade LOD.
While alternative detection strategies
and microcolumn geometries have been employed
to improve LOD, sample enrichment methods, both
preconcentration and in-line concentration, have
also been very successfully utilized to bring
analytes up to the detection limits of the common
detectors using standard capillary instruments.
Our research
places heavy emphasis on electrophoretic sample
enrichment techniques for CE and microfluidics to
perform the trace analysis requirements of bioanalytical
problems. A major area of investigation is
utilization of electrophoretic focusing methods,
which incorporate simultaneous separation and concentration
enhancement, for trace measurements using more universal
detectors than fluorescence ( e.g. , UV
absorbance, Raman spectroscopy, etc. ),
which also mitigate the need for analyte labeling
prior to detection. A second area of interest
is evaluating the efficacy of counter-flow electrophoretic
separations for isolating and quantifying analytes
from complex mixtures, such as from biological fluids,
with little or no sample preparation. Additionally,
multi-dimensional combinations of the techniques
are being investigated for performing both trace
analyses and complex composition separations.
All methods are being developed with the intent
of implementation in microfluidic formats to promote
integration, transferability, and automation for
biochemical monitoring.
|