SBIR Phase I: Biomolecular Detection of microRNA

Award Information
Agency:
National Science Foundation
Branch
n/a
Amount:
$150,000.00
Award Year:
2011
Program:
SBIR
Phase:
Phase I
Contract:
1047285
Award Id:
n/a
Agency Tracking Number:
1047285
Solicitation Year:
2010
Solicitation Topic Code:
BC
Solicitation Number:
n/a
Small Business Information
3913 Todd Lane Suite 312, Austin, TX, 78744-1057
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
Y
Duns:
611930244
Principal Investigator:
Masoud Toloue
(512) 707-8993
mtoloue@biooscientific.com
Business Contact:
Masoud Toloue
DPhil
(512) 707-8993
mtoloue@biooscientific.com
Research Institute:
Stub




Abstract
This Small Business Innovation Research (SBIR) Phase I project proposes to examine high throughput methods to quantify intacellular microRNA (miRNA) concentrations in cells that have shown to be associated with normal physiological processes as well as diseases including cancer. Currently, there are no rapid, quantitative methods available to measure miRNA expression in living cells or tumor tissue. All current in vitro approaches require extensive preparation involving extraction, reverse transcription of miRNA into cDNA, and amplification. These methods are not only time consuming, but require that the low abundance miRNA be several fold greater than background to give a significant result. To meet the demand for a diagnostic/prognostic tool, we propose development of a biomolecular detection device based on a single electron transistor to bind and measure the concentration of miRNAs, giving a researcher or clinician an accurate profile to make proper clinical assessments. In addition, we propose development of fluorescent probes designed to bind to miRNAs intra-cellularly and fluoresce upon recognition. Developing these high-throughput methods to detect miRNA at the single cell level will give us direct information on intracellular miRNA levels, miRNAs that are essential for identifying tumor maintenance or metastasis, thus creating new diagnostic and therapeutic opportunities. The broader/commercial impact of this project will be to enhance current diagnostic and prognostic tools for early detection of disease. Today, early cancer detection and treatment offers the best outcome for patients. This has driven the search for effective diagnostics. The identification of a universal tumor-specific epitope or marker has remained elusive. While many types of serological and serum markers have included enzymes, proteins, hormones, mucin, and blood group substances, at this time there are no effective diagnostic tests for cancer that are highly specific, sensitive, economical and rapid. This deficiency means that many cases of malignancy go undetected long past the time of effective treatment. The goal of this research is to develop clinical diagnostic tools where miRNA profiles can be examined from patient samples immediately in a hospital or clinical setting. The current size of the in vitro diagnostic market is estimated to be over $40 billion. Unique diagnostic kits developed from this technology will likely fulfill an unmet market opportunity with the potential to exceed $100 million in the first 3 - 5 years.

* information listed above is at the time of submission.

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