SBIR-STTR Award

Rapid, Label-Free, Multiplex Detection Of Micrornas
Award last edited on: 5/18/11

Sponsored Program
SBIR
Awarding Agency
NIH : NCI
Total Award Amount
$99,521
Award Phase
1
Solicitation Topic Code
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Principal Investigator
Mary S Rosendahl

Company Information

Riot Platforms Inc (AKA: Riot Blockchain Inc~BiOptix Diagnostics Inc~AlphaSniffer LLC)

3855 Ambrosia Street Suite 301
Castle Rock, CO 80109
   (303) 794-2000
   N/A
   www.riotplatforms.com
Location: Single
Congr. District: 04
County: Douglas

Phase I

Contract Number: 1R43CA153467-01
Start Date: 9/17/10    Completed: 3/16/11
Phase I year
2010
Phase I Amount
$99,521
Minimally invasive tests for the detection and monitoring of malignancies are urgently needed worldwide to reduce the morbidity and mortality caused by cancer. While promising, blood-based proteonomic assays have yet to be clinically validated for many common human cancers. Accordingly, new approaches are being investigated that will likely complement or improve on current strategies. In particular, microRNAs (miRNAs) have gained considerable attention as potentially predictive biomarkers for a number of disorders. This Phase I research project will evaluate the feasibility of rapid, label-free identification and quantification of miRNAs from blood samples using a novel ultra-sensitive detection technology known as Surface Plasmon Enhanced Common Path Interferometry (SPE-CPI). SPE-CPI differs from standard Surface Plasmon Resonance (SPR) detection methods, such as Biacore, in that it combines the high sensitivity of SPR with the higher stability and lower noise of a CPI single-beam path. SPE- CPI also allows for the simultaneous monitoring of multiple species of miRNA in a single sample. During Phase I, SPE-CPI based protocols for measuring cancer-related miRNAs in the presence of serum will be identified and qualified. Specificity and limit of detection will be critical parameters for this proof-of-feasibility study. Further, using the optimized SPE-CPI methods, we will evaluate the potential of SPE-CPI as a diagnostic tool for the detection of miRNAs using serum samples from patients with lung cancer versus healthy individuals. If successful, this research will be a major step forward in new diagnostic strategies for cancer and possibly other diseases that may be modulated by miRNA. Advancements in label-free sensing technologies will also open broader applications for the measurement of low abundance proteins, protein- protein interaction studies, infectious disease detection, biowarfare pathogen detection, protein- drug interactions, food safety, detection of chemical pollutants, and the like. The SPE-CPI instrument that will be evaluated in these studies is small, inexpensive, and requires minimal sample manipulation for analysis. Affordable, easy-to use detectors for rapid screening at point of care facilities, i.e. doctors'offices, would be a significant breakthrough in the health care industry. , ,

Public Health Relevance:
This Small Business Innovation Research (SBIR) Phase I project will evaluate an ultra-sensitive detection technology for the non-invasive multiplex quantification of lung cancer biomarkers in serum samples. If successful, this research will be a major step forward in a new strategy for point of care diagnosis of cancer and other diseases. Advancements in biosensor technologies will also open broader applications for the measurement of low abundance proteins, protein-protein interaction studies, infectious disease detection, biowarfare pathogen detection, protein-drug interactions, vaccine development, food safety, detection of chemical pollutants, and the like.

Thesaurus Terms:
Assay;Attention;Binding;Binding (Molecular Function);Bioassay;Biologic Assays;Biologic Warfare;Biological Assay;Biological Warfare;Biosensor;Blood;Blood Sample;Blood Serum;Blood Specimen;Cancer Cause;Cancer Etiology;Cancer Patient;Cancer Of Lung;Cancers;Chemicals;Chemistry;Clinical;Colorado;Communicable Diseases;Complement;Complement Proteins;Detection;Diagnostic;Disease;Disorder;Drug Interactions;Feasibility Studies;Food Safety;Gene Products, Rna;Glass;Goals;Health Care Industry;Healthcare Industry;Human;Human, General;Individual;Industry, Healthcare;Infectious Disease Pathway;Infectious Diseases;Infectious Diseases And Manifestations;Infectious Disorder;Interferometry;Lna (Nucleic Acid);Label;Malignant Neoplasms;Malignant Tumor;Malignant Tumor Of The Lung;Malignant Neoplasm Of Lung;Man (Taxonomy);Man, Modern;Measurement;Measures;Methods;Micro Rna;Micrornas;Modeling;Modification;Molecular Interaction;Monitor;Morbidity;Morbidity - Disease Rate;Mortality;Mortality Vital Statistics;Noise;Oligo;Oligonucleotide Probes;Oligonucleotides;Oligoribonucleotides;Pathogen Detection;Patients;Performance;Phase;Preparation;Proteins;Protocol;Protocols Documentation;Pulmonary Cancer;Pulmonary Malignant Neoplasm;Qualifying;R01 Mechanism;R01 Program;Rna;Rna, Non-Polyadenylated;Rpg;Research;Research Grants;Research Project Grants;Research Projects;Research Projects, R-Series;Reticuloendothelial System, Blood;Ribonucleic Acid;Sbir;Sbirs (R43/44);Sampling;Science Of Chemistry;Screening Procedure;Sensitivity And Specificity;Serum;Small Business Innovation Research;Small Business Innovation Research Grant;Specificity;Surface;Surface Plasmon Resonance;Technology;Testing;Universities;Work;Assay Development;Base;Biomarker;Biowarfare;Cancer Diagnosis;Clinical Relevance;Clinically Relevant;Detector;Disease/Disorder;Gene Product;Improved;Instrument;Locked Nucleic Acid;Lung Cancer;Malignancy;Meetings;Mirna;Minimally Invasive;Multiplex Detection;Neoplasm/Cancer;New Approaches;New Diagnostics;Next Generation;Next Generation Diagnostics;Novel;Novel Approaches;Novel Diagnostics;Novel Strategies;Novel Strategy;Point Of Care;Pollutant;Protein Protein Interaction;Prototype;Public Health Relevance;Screening;Screenings;Sensor (Biological);Tool;Vaccine Development

Phase II

Contract Number: ----------
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
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Phase II Amount
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