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Multimodality Photoacoustic and Raman Imaging

  • Author / Creator
    Shi, Wei
  • Tumor metastasis is referred to the spread of cancer from one to another unadjacent part of the body, which results in more than 90% of tumor deaths, and however is still poorly understood. Circulating tumor cells (CTCs) have been proposed as an important biomarker of tumor metastasis. Many approaches have been developed for detection of CTCs, but each has its own advantages and disadvantages. With the aid of nanoparticles (NPs), photoacoustic detection along with efficient magnetic enrichment of CTCs demonstrated high sensitivity. However, differentiation of photoacoustic signals is non-trivial hence specificity can be poor. Surface-enhanced-Raman-scattering (SERS) NPs were used for detection of CTCs with high multiplexing capability. However, the lack of enrichment of CTCs limits its application for in vivo detection. High sensitivity and high specificity in vivo methods of detecting CTCs are in urgent need. A hallmark signature of metastasis is angiogenesis, the proliferation of vessel networks growing from pre-existing vasculature. Imaging angiogenesis is important for cancer research since angiogenesis is regarded as a necessity for tumor growth and tumor metastasis. Photoacoustic imaging (PAM) is a promising technique for imaging angiogenesis due to intrinsic high optical contrast between blood and tissues, and high spatial resolution at adequate penetration depth. Optical-resolution photoacoustic imaging (OR-PAM) pushed the lateral resolution limit of PAM to micron or submicron level, which enables imaging of single capillaries, the finest vasculature elements. However, the low imaging speed of OR-PAM may limit its application in the clinic, and for practical pre-clinical imaging of animal models. A single modality tool for studies on tumor metastasis is unlikely to be able to fullfill these needs. Therefore, the long term goal of this dissertation is to develop a multimodality imaging tool for imaging tumor metastasis and detecting of CTCs with high specificity and high sensitivity. Specially, we focused on the approach of combing PAM with a Raman imaging technology for this purpose. For the task of detecting CTCs, the photoacoustic subsystem could aid in placement of a magnet for trapping of such CTCs and gaging the flow rate for optimal optical and multiplexed detection with the Raman sub-system. The photoacoustic sub-system could also be used for detecting absorption signatures from nanoparticles on tumor cells. For detecting metastases, the Raman imaging subsystem could be used to detect multiple flavors of nanoparticles targeted to (non-circulating) tumor cells and the photoacoustic sub-system could be used to detect neoplasm angiogenesis. We aimed to push limits of OR-PAM imaging frame-rate, to develop a novel CTC detection technique with high sensitivity and high specificity, and to further build a multimodality photoacoustic-Raman imaging tool for high sensitivity and high specificity molecular imaging. Our work presented in this dissertation can be divided into three parts. First, we worked on developing realtime OR-PAM using various high pulse repetition rate lasers and combined with a fast optical scanning galvanometer mirror systems. We reported the first near realtime volumetric OR-PAM with 4 frames per second (fps) imaging speed and ~ 6 m lateral resolution by employing a fiber laser with up to 600 kHz pulse repetition rate. Further, we demonstrated in vivo near realtime sustained OR-PAM imaging of dynamic process and 30 fps realtime imaging of cardiac-induced mircrohemodynamics in murine microvasculature. In addition, we studied the scanning speed dependence of photoacoustic signals which may lead to a super-resolution technique in the future. Second, we demonstrated for the first time the magnetic enrichment and detection of CTCs in circulating PBS or rat blood with high specificity and high sensitivity by targeting tumor cells with both SERS NPs and magnetic NPs (MNPs). Third, we presented a multimodality imaging system consisting of PAM and SERS imaging which may advance the research of tumor metastasis in the future.

  • Subjects / Keywords
  • Graduation date
    2014-11
  • Type of Item
    Thesis
  • Degree
    Doctor of Philosophy
  • DOI
    https://doi.org/10.7939/R3P55DN81
  • License
    This thesis is made available by the University of Alberta Libraries with permission of the copyright owner solely for non-commercial purposes. This thesis, or any portion thereof, may not otherwise be copied or reproduced without the written consent of the copyright owner, except to the extent permitted by Canadian copyright law.
  • Language
    English
  • Institution
    University of Alberta
  • Degree level
    Doctoral
  • Department
    • Department of Electrical and Computer Engineering
  • Specialization
    • Biomedical Engineering
  • Supervisor / co-supervisor and their department(s)
    • Zemp, Roger (Electrical and Computer Engineering)
  • Examining committee members and their departments
    • Fedosejevs, Robert ( Electrical and Computer Engineering)
    • Lewis, John (Department of Oncology)
    • Wilson, Brian (Department of Medical Biophysics, University of Toronto/University Health Network)
    • DeCorby, Ray ( Electrical and Computer Engineering)