SBIR-STTR Award

Handheld Gene Analyzer based on dye-doped nanoparticles
Award last edited on: 11/18/05

Sponsored Program
STTR
Awarding Agency
NIH : NIAID
Total Award Amount
$620,222
Award Phase
2
Solicitation Topic Code
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Principal Investigator
Monde T Qhobosheane

Company Information

Life Sciences Inc (AKA: Foshan Life Sciences)

2900 72nd Street North
St Petersburg, FL 33710
   (727) 345-9371
   lsi1@gte.net
   www.lifesci.com

Research Institution

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Phase I

Contract Number: 1R43AI060321-01
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
2004
Phase I Amount
$242,880
Life Sciences proposes the development of a novel pathogen detection system based on dye-doped nanoparticles (NPs) and supported by low cost, field portable instrumentation to facilitate the rapid detection of nucleic acid sequences present in low copy number; with or without amplification. Silica, dye-doped NPs to be used in this effort have been demonstrated to produce 10,000 to 100,000 fold increases in detectable signal from a single hybridization event with a DNA target when compared to commonly used fluorescent reporters. This high level of signal enhancement is expected to permit the use, with optimization, of an existing low cost, field portable fluorometer to support the application of the pathogen detection in products for rapid (10 minutes) low cost ($ 5-10 per test) for point-of collection diagnosis of infectious disease. The system may also be deployed for field detection and identification of environmental pathogens in food and water, to include agents that maybe employed as biological weapons. To achieve this goal there are two aims in this proposal. First, we will develop a novel DNA/RNA bioassay based on dye-doped NP. This assay will be performed on glass substrate and detected by a traditional spectrofluorometer. NP optimization will be completed and will emphasize smaller size, higher signal intensity, and ease of bioconjugation. Secondly, we intend to optimize an existing low-cost fluorometer such that it can be employed as a handheld gene detection analyzer. This part will be performed on magnetic beads and detected by the hand-held fluorometer. We will focus the immobilization of DNA on the surface of magnetic beads, optimization of the assay to detect DNA down to picomole range. More importantly, we will emphasize the combination of the hand-held fluorometer to the assay. Our project is an integrated one in which better NPs will be prepared, ultrasensitive optical detection systems will be optimized, NP bioconjugation and surface chemistry will be better understood and improved, new insights into NP's bioanalytical applications will be obtained, and portable protocols for ultrasensitive bioanalysis will be developed and utilized.

Thesaurus Terms:
biohazard detection, biomedical equipment development, communicable disease diagnosis, miniature biomedical equipment, nanotechnology, portable biomedical equipment, rapid diagnosis bioassay, diagnosis design /evaluation, nucleic acid quantitation /detection, silicate biotechnology, bioterrorism /chemical warfare, fluorimetry, nucleic acid hybridization

Phase II

Contract Number: 5R41AI060321-02
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
2005
Phase II Amount
$377,342
Life Sciences proposes the development of a novel pathogen detection system based on dye-doped nanoparticles (NPs) and supported by low cost, field portable instrumentation to facilitate the rapid detection of nucleic acid sequences present in low copy number; with or without amplification. Silica, dye-doped NPs to be used in this effort have been demonstrated to produce 10,000 to 100,000 fold increases in detectable signal from a single hybridization event with a DNA target when compared to commonly used fluorescent reporters. This high level of signal enhancement is expected to permit the use, with optimization, of an existing low cost, field portable fluorometer to support the application of the pathogen detection in products for rapid (10 minutes) low cost ($ 5-10 per test) for point-of collection diagnosis of infectious disease. The system may also be deployed for field detection and identification of environmental pathogens in food and water, to include agents that maybe employed as biological weapons. To achieve this goal there are two aims in this proposal. First, we will develop a novel DNA/RNA bioassay based on dye-doped NP. This assay will be performed on glass substrate and detected by a traditional spectrofluorometer. NP optimization will be completed and will emphasize smaller size, higher signal intensity, and ease of bioconjugation. Secondly, we intend to optimize an existing low-cost fluorometer such that it can be employed as a handheld gene detection analyzer. This part will be performed on magnetic beads and detected by the hand-held fluorometer. We will focus the immobilization of DNA on the surface of magnetic beads, optimization of the assay to detect DNA down to picomole range. More importantly, we will emphasize the combination of the hand-held fluorometer to the assay. Our project is an integrated one in which better NPs will be prepared, ultrasensitive optical detection systems will be optimized, NP bioconjugation and surface chemistry will be better understood and improved, new insights into NP's bioanalytical applications will be obtained, and portable protocols for ultrasensitive bioanalysis will be developed and utilized.

Thesaurus Terms:
biohazard detection, biomedical equipment development, communicable disease diagnosis, miniature biomedical equipment, nanotechnology, portable biomedical equipment, rapid diagnosis bioassay, diagnosis design /evaluation, nucleic acid quantitation /detection, silicate biotechnology, bioterrorism /chemical warfare, fluorimetry, nucleic acid hybridization