Grant: Discovery Grants Program - Individual
Ryerson University
$51,000.00
Static and dynamic light and ultrasound measurements for the elucidation of biological and biomaterial structure and function
EF 2014-15
Résumé
The objective of the proposal is to develop optical and ultrasound techniques to characterise the functional state of cells and tissues using optical, ultrasound and photoacoustic techniques. My work to date has been focused on using static optical and ultrasound scattering. In the proposed work these static techniques will be refined based on new knowledge generated from recent theoretical and experimental findings. The main novelty of the new work proposed will be a) to extend the techniques developed to include photoacoustic tissue characterization and b) to extended the static ultrasound and optical scattering measurements to include dynamic scattering measurements (fluctuations of scattering intensity as a function of time) to infer the states of cells and tissues. Whereas the field of photoacoustic imaging has recently gained a lot of attention, fundamental questions as to the origin of the photoacoustic signal and how to characterize the signal when blood vessels (the main generator of photoacoustic signals) are unresolved remain unanswered. As for most clinically relevant ultrasound frequencies blood vessels of interest cannot be resolved, a new technique is required to analyze the photoacoustic signals. New techniques based on modeling the photoacoustic signals generated by individual blood vessels will be used to develop methods for photoacoustic tissue characterization. In parallel, techniques will be also developed based on the fluctuations of (optical / ultrasound) scattering intensity as a function of time. We recently discovered that dying cells exhibit significantly shorter optical coherence tomography speckle decorrelation times (faster fluctuations of scattering intensity as a function of time), and that the speckle decorrelation time can be used to assess intracellular motion of the main scattering sources within cells / tissues. While the most common application relates to blood flow measurements, in these new techniques signals from blood are supressed so as to assess motion in tissues and cells alone. The optical and ultrasound techniques developed will aid in the non-invasive monitoring of the functional states of cells and tissues.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
216986-2012
Name nom
Kolios, Michael
Department département
Physics
Organization id
43
Institution établissement
Ryerson University
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2014
Competition year année de concours
2012
Award amount
51000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1505
Committee name en
Physics
Committee name fr
Physique
Area of application code
1211
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Medical and health sciences
Area of application fr
Sciences médicales et de la santé
Research subject code
3114
Research subject group en
Physics
Research subject group fr
Physique
Research subject en
Biological and Medical Physics
Research subject fr
Physique biologique et médicale
Partie
3
Nb partie
5
Application title
Static and dynamic light and ultrasound measurements for the elucidation of biological and biomaterial structure and function
Keyword
NSERC
Application summary
The objective of the proposal is to develop optical and ultrasound techniques to characterise the functional state of cells and tissues using optical, ultrasound and photoacoustic techniques. My work to date has been focused on using static optical and ultrasound scattering. In the proposed work these static techniques will be refined based on new knowledge generated from recent theoretical and experimental findings. The main novelty of the new work proposed will be a) to extend the techniques developed to include photoacoustic tissue characterization and b) to extended the static ultrasound and optical scattering measurements to include dynamic scattering measurements (fluctuations of scattering intensity as a function of time) to infer the states of cells and tissues. Whereas the field of photoacoustic imaging has recently gained a lot of attention, fundamental questions as to the origin of the photoacoustic signal and how to characterize the signal when blood vessels (the main generator of photoacoustic signals) are unresolved remain unanswered. As for most clinically relevant ultrasound frequencies blood vessels of interest cannot be resolved, a new technique is required to analyze the photoacoustic signals. New techniques based on modeling the photoacoustic signals generated by individual blood vessels will be used to develop methods for photoacoustic tissue characterization. In parallel, techniques will be also developed based on the fluctuations of (optical / ultrasound) scattering intensity as a function of time. We recently discovered that dying cells exhibit significantly shorter optical coherence tomography speckle decorrelation times (faster fluctuations of scattering intensity as a function of time), and that the speckle decorrelation time can be used to assess intracellular motion of the main scattering sources within cells / tissues. While the most common application relates to blood flow measurements, in these new techniques signals from blood are supressed so as to assess motion in tissues and cells alone. The optical and ultrasound techniques developed will aid in the non-invasive monitoring of the functional states of cells and tissues.