SBIR/STTR Research Award

Fluorescence Lifetime Dynamics to Understand Brain Neural Activities and Behavior

Award identifier 768889cab2eb11b20b9ea2a6e465bb13343754acc8ca2ede2c6b23edd2bdfffeAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$679,678

Program and phase

SBIR · Phase I

Award year

2014

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
CHISQUARE BIOIMAGING LLC
Proposal award date
2014-09-20
Contract end date
2016-08-31
UEI
NVLJCFLWHA36
Solicitation number
PA11-134
Topic code
500

Research abstract

DESCRIPTION provided by applicant The overall objective of the proposed project is to create a compact robust and easy to use device that is capable of sensitive and quantitative detection of fluorescence lifetime indicators of physiological and biochemical dynamics deep in the brain of a freely moving mouse In contrast to fluorescence intensity based methods fluorescence lifetime can delineate spectrally overlapping fluorescent signals Our focus is on measurements related to alcohol addiction and behavior in the striatum and other structures deep inside the brain Most in vivo mouse brain studies are based on the fluorescence intensity measurements However for measurements of more than one fluorophore we face challenges of mixed or overlapping emission spectra which complicates the quantitative interpretation of the results In Cui et al Nature was the first to introduce fluorescence lifetime asa measurement parameter in examining the relationship between neural activities in a freely moving mouse and behavior deep in the brain area of the striatum It has provided the first definitive evidence that direct and indirect pathway striatal neurons are co activated during movement initiation and are inactive when the animal is not moving Inspired by the success of their device we will collaborate with the original authors to develop this instrument to a device for general applicability in neuroscience labs to investigate alcohol addiction Aim is to develo a prototype instrument and in house testing This includes constructing main body of the device by integrating the time correlated single photon counting TCSPC electronics the pulse laser source and single photon detector incorporating innovative in vivo probe designs and fiber coupling technology and to perform rigorous testing and calibration to validate the new design Aim is to have the device tested at neuroscience labs for the iterative process of testing and modification Months Three aspects make our device truly innovative and the first of its kind Firstly fluorescence lifetime detection makes it possible to distinguish the source of fluorescent signals despite their mixed or overlapping emission spectra Secondly our fiber optics based in vivo probes will be designed to shape the excitation and detection volume for efficient signal throughput and be combined with the latest technology in highest efficiency coupling to offer a flexible on off connection to the implantable in vivo probe Thirdly our desig will result in a compact robust and easy to use device with versatile interchangeable in vivo probes We anticipate that this device will make fluorescence lifetime detection technology the method of choice for investigations where it can add a definitive contrasting mechanism and specificity We envision that the combination of fluorescence lifetime detection with fluorescent proteins allows for a wide range of applications and will be used for studies involving photoactivation voltage sensing redox sensing and calcium sensing and release and to examine protein protein interactions using fluorescence lifetime and Firster resonance energy transfer FLIM FRET PUBLIC HEALTH RELEVANCE We propose to develop a compact robust easy to use device that is capable of measuring dynamic biochemical and electrical signals in the brain of a freely moving rodent Understanding the relationship between neural activities in the brain of an experimental model system and its behavior will be a step forward in understanding how that relationship might work in human The device that we have proposed in this application will implement fluorescence lifetime detection using time correlated single photon counting as its core technology This method has a distinct advantage in resolving complex fluorescence signals from more than one source and will lead to more accurate interpretation of biological signals in the brain The immediate application of this device is in understanding the signaling pathways that control behavior related to drug seeking and their roles in alcohol addiction However the device will find a broad range of applications in the studies related to Parkinsonandapos s disease Alzheimerandapos s disease and other neurological based diseases

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

2 SBIR/STTR records share this UEI (2014–2019). Reported award amounts total $904,360. Reported amounts are not federal obligations.

Phases: Phase I

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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