10 results match your criteria: "CanadabUniversity of Toronto[Affiliation]"

Can photoacoustic imaging quantify surface-localized J-aggregating nanoparticles?

J Biomed Opt

July 2017

University Health Network, Princess Margaret Cancer Centre, Toronto, Ontario, CanadabUniversity of Toronto, Department of Medical Biophysics, Toronto, Ontario, Canada.

We investigate the feasibility of photoacoustic (PA) imaging to quantify the concentration of surface-localized nanoparticles, using tissue-mimicking phantoms and imaging with a commercial PA instrument at 815 nm and a linear-array transducer at a center frequency of 40 MHz. The nanoparticles were J-aggregating porphysomes (JNP) comprising self-assembling, all-organic porphyrin-lipid micelles with a molar absorption coefficient of 8.7×108  cm−1 M−1 at this wavelength.

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Shape-based reconstruction for transrectal diffuse optical tomography monitoring of photothermal focal therapy of prostate cancer: simulation studies.

J Biomed Opt

April 2017

University Health Network, Techna Institute, Toronto, Ontario, CanadaeUniversity of Toronto, Department of Medical Biophysics, Toronto, Ontario, CanadafUniversity Health Network, Ontario Cancer Institute, Toronto, Ontario, Canada.

We develop and demonstrate a simple shape-based approach for diffuse optical tomographic reconstruction of coagulative lesions generated during interstitial photothermal therapy (PTT) of the prostate. The shape-based reconstruction assumes a simple ellipsoid shape, matching the general dimensions of a cylindrical diffusing fiber used for light delivery in current clinical studies of PTT in focal prostate cancer. The specific requirement is to accurately define the border between the photothermal lesion and native tissue as the photothermal lesion grows, with an accuracy of ? 1 ?? mm , so treatment can be terminated before there is damage to the rectal wall.

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Porphysome nanoparticles for enhanced photothermal therapy in a patient-derived orthotopic pancreas xenograft cancer model: a pilot study.

J Biomed Opt

August 2016

University Health Network, Princess Margaret Cancer Center, 101 College Street, Toronto, Ontario M5G 1L7, CanadabUniversity of Toronto, Department of Medical Biophysics, 101 College Street, Toronto, Ontario M5G 1L7, CanadacPrincess Margaret Hospital, Department of Medical Oncology and Hematology, 610 University Avenue, Toronto, Ontario M5T 2M9, Canada.

Local disease control is a major challenge in pancreatic cancer treatment, because surgical resection of the primary tumor is only possible in a minority of patients and radiotherapy cannot be delivered in curative doses. Despite the promise of photothermal therapy (PTT) for focal ablation of pancreatic tumors, this approach remains underinvestigated. Using photothermal sensitizers in combination with laser light irradiation for PTT can result in more efficient conversion of light energy to heat and improved spatial confinement of thermal destruction to the tumor.

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Polyacrylamide gel substrates that simulate the mechanical stiffness of normal and malignant neuronal tissues increase protoporphyin IX synthesis in glioma cells.

J Biomed Opt

September 2015

Princess Margaret Cancer Centre, 101 College Street, Toronto, Ontario M5G1L7, CanadabUniversity of Toronto, Department of Medical Biophysics, 101 College Street, Toronto, Ontario M5G1L7, Canada.

Protoporphyrin IX (PPIX) produced following the administration of exogenous 5d-aminolevulinic acid is clinically approved for photodynamic therapy and fluorescence-guided resection in various jurisdictions around the world. For both applications, quantification of PPIX forms the basis for accurate therapeutic dose calculation and identification of malignant tissues for resection. While it is well established that the PPIX synthesis and accumulation rates are subject to the cell’s biochemical microenvironment, the effect of the physical microenvironment, such as matrix stiffness, has received little attention to date.

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This study compares fluorescence and photoacoustic (PA) imaging of ex vivo tumors and organs from tumor-bearing mice injected intravenously with ultrasmall (<3  nm ) tiopronin-capped Au nanoparticles and compares the data with inductively coupled plasma mass spectrometry (ICP-MS). Good agreement is seen in particle distributions and concentrations at the organ level. The spatial resolution from the imaging techniques allows for localization of the particles within organ structures.

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Polarized light imaging in biomedicine: emerging Mueller matrix methodologies for bulk tissue assessment.

J Biomed Opt

June 2015

University of Toronto, Division of Biophysics and Bioimaging, Ontario Cancer Institute/University Health Network and Department of Medical Biophysics, 101 College Street, Toronto, Ontario MG 1L7, CanadabUniversity of Toronto, Department of Radiation Oncol.

Polarized light point measurements and wide-field imaging have been studied for many years in an effort to develop accurate and information-rich tissue diagnostic methods. However, the extensive depolarization of polarized light in thick biological tissues has limited the success of these investigations. Recently, advances in technology and conceptual understanding have led to a significant resurgence of research activity in the promising field of bulk tissue polarimetry.

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Dynamic light scattering arising from flowing Brownian particles: analytical model in optical coherence tomography conditions.

J Biomed Opt

December 2014

University of Toronto, Department of Medical Biophysics, Room 15-301M, Toronto Medical Discovery Tower, 101 College Street, Toronto, Ontario M5G 1L7, CanadabUniversity of Toronto, Department of Radiation Oncology, 610 University Avenue, Toronto, Ontario M.

The statistical model of scattered by flowing Brownian particles coherent radiation is suggested. The model includes the random Doppler shifts caused by particle Brownian motion and the speckle fluctuations caused primarily by the flow motion of particles. Analytical expressions are obtained for the correlation function, power spectrum, and spectral width of scattered radiation in the imaging geometry typically used in optical coherence tomography (OCT).

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Autofluorescence imaging device for real-time detection and tracking of pathogenic bacteria in a mouse skin wound model: preclinical feasibility studies.

J Biomed Opt

August 2014

University Health Network, Princess Margaret Cancer Centre, 610 University Avenue, Toronto, Ontario M5G 2M9, CanadabUniversity of Toronto, Department of Medical Biophysics, Faculty of Medicine, 1 King's College Circle, Toronto, Ontario M5S 1A8, CanadaeUni.

Bacterial infection significantly impedes wound healing. Clinical diagnosis of wound infections is subjective and suboptimal, in part because bacteria are invisible to the naked eye during clinical examination. Moreover, bacterial infection can be present in asymptomatic patients, leading to missed opportunities for diagnosis and treatment.

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Delayed near-infrared analysis permits visualization of rodent retinal pigment epithelium layer in vivo.

J Biomed Opt

February 2015

University of Toronto, Department of Laboratory Medicine and Pathobiology, 1 King's College Circle, Toronto, Ontario M5S 1A8, CanadabUniversity of Toronto, Department of Ophthalmology and Vision Sciences, 340 College Street, Toronto, Ontario M5T 3A9, Cana.

Patches of atrophy of the retinal pigment epithelium (RPE) have not been described in rodent models of retinal degeneration, as they have the clinical setting using fundus autofluorescence. We hypothesize that prelabeling the RPE would increase contrast and allow for improved visualization of RPE loss in vivo. Here, we demonstrate a new technique termed “delayed near-infrared analysis (DNIRA)” that permits ready detection of rat RPE, using optical imaging in the near-infrared (IR) spectrum with aid of indocyanine green (ICG) dye.

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Second harmonic generation polarization properties of myofilaments.

J Biomed Opt

May 2014

University of Toronto, Department of Physics and Institute for Optical Sciences, 60 Saint George Street, Toronto, Ontario M5S1A7, CanadabUniversity of Toronto Mississauga, Department of Chemical and Physical Sciences, 3359 Mississauga Road North, Mississa.

Second harmonic generation (SHG) polarization microscopy was used to investigate the organization of myosin nanomotors in myofilaments of muscle cells. The distribution of the second-order nonlinear susceptibility component ratio χzzz(2)/χzxx(2) along anisotropic bands of sarcomeres revealed differences between the headless and head-containing regions of myofilaments. The polarization-in polarization-out SHG measurements of headless myosin mutants of indirect flight muscle in Drosophila melanogaster confirmed a lower susceptibility component ratio compared to the head-containing myocytes with wild-type myosins.

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