The proposed R21/R33 application """"""""Micro Lock-In Amplifier for Cortisol and Catecholamines"""""""" will explore the design hypothesis that a new microimmunoassay device can rapidly detect multiple analytes in saliva to better understand the effect of stress on health. Stress in general and cortisol, specifically, has links to cardiovascular health, bone density, diabetes, obesity, autoimmune disease, reproductive health, and cognition. The proposed new system would bring advances in miniaturization and magnetorheology together to improve the detection limit in competitive immunoassays through a lock-in amplifier signal conditioning system. Multi-channel competitive immunoassays for rapid quantitation of analytes in saliva are sought as a means to simultaneously visualize time-dependent changes in biomarkers of stress, such as cortisol, as a risk for disease. Saliva sample collection is desired over blood and other bodily fluids for many reasons. In our proposed research, the most important purpose for using saliva is the promise of drawing samples quickly in order to catch dynamic responses. Currently, cortisol and catecholamines are measured individually and usually from blood. In collection of blood for cortisol analysis care must be taken with cannula insertion, and there must be a 45 minute wait after cannula insertion to draw the first baseline sample. Thus, use of blood samples and cannula use, can limit situations in which cortisol measurements can be taken. It can also limit the populations that can be studied as well, since there is a reluctance to use the cannulas in children, and sometimes in older subjects as well. The outcome from this research is the expansion of the current suite of analytes measurable in saliva and the streamlining of sample collection and processing to """"""""image"""""""" bodily responses to stress and other external stimuli. Applications to wellness, therapeutic drug monitoring, and bio or chemical exposure are envisioned using the general approach of microlock-in amplifier detection technology. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21EB000679-02
Application #
6663160
Study Section
Special Emphasis Panel (ZRG1-SSS-F (02))
Program Officer
Korte, Brenda
Project Start
2002-09-30
Project End
2005-02-28
Budget Start
2003-09-01
Budget End
2005-02-28
Support Year
2
Fiscal Year
2003
Total Cost
$186,875
Indirect Cost
Name
Arizona State University-Tempe Campus
Department
Biomedical Engineering
Type
Schools of Engineering
DUNS #
943360412
City
Tempe
State
AZ
Country
United States
Zip Code
85287
Petkus, Matthew M; McLauchlin, Melissa; Vuppu, Anil K et al. (2006) Detection of FITC-cortisol via modulated supraparticle lighthouses. Anal Chem 78:1405-11