5 results match your criteria: "United StatesbWashington University in St. Louis[Affiliation]"

Multimodal fluorescence molecular imaging for in vivo characterization of skin cancer using endogenous and exogenous fluorophores.

J Biomed Opt

June 2017

Washington University School of Medicine, Mallinckrodt Institute of Radiology, Optical Radiology Laboratory, St. Louis, Missouri, United StatesbWashington University in St. Louis, Biomedical Engineering, St. Louis, Missouri, United States.

Similarity of skin cancer with many benign skin pathologies requires reliable methods to detect and differentiate the different types of these lesions. Previous studies have explored the use of disparate optical techniques to identify and estimate the invasive nature of melanoma and basal cell carcinoma with varying outcomes. Here, we used a concerted approach that provides complementary information for rapid screening and characterization of tumors, focusing on squamous cell carcinoma (SCC) of the skin.

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Generation of anatomically realistic numerical phantoms for photoacoustic and ultrasonic breast imaging.

J Biomed Opt

April 2017

Washington University in St. Louis, Department of Biomedical Engineering, 1 Brookings Drive, St. Louis, Missouri 63130, United StatesbWashington University in St. Louis, Department of Electrical and Systems Engineering, 1 Brookings Drive, St. Louis, Missouri 63130, United StatescWashington University in St. Louis, Mallinckrodt Institute of Radiology, 1 Brookings Drive, St. Louis, Missouri 63130, United States.

Photoacoustic computed tomography (PACT) and ultrasound computed tomography (USCT) are emerging modalities for breast imaging. As in all emerging imaging technologies, computer-simulation studies play a critically important role in developing and optimizing the designs of hardware and image reconstruction methods for PACT and USCT. Using computer-simulations, the parameters of an imaging system can be systematically and comprehensively explored in a way that is generally not possible through experimentation.

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Photoacoustic microscopy of arteriovenous shunts and blood diffusion in early-stage tumors.

J Biomed Opt

February 2016

Washington University in St. Louis, Department of Electrical and Systems Engineering, One Brookings Drive, St. Louis, Missouri 63130, United StatesbWashington University in St. Louis, Department of Biomedical Engineering, One Brookings Drive, St. Louis, M.

Angiogenesis in a tumor region creates arteriovenous (AV) shunts that cause an abnormal venous blood oxygen saturation ( sO2 ) distribution. Here, we applied optical-resolution photoacoustic microscopy to study the AV shunting in vivo. First, we built a phantom to image sO2 distribution in a vessel containing converged flows from two upstream blood vessels with different sO2 values.

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Experimental validation of a high-resolution diffuse optical imaging modality: photomagnetic imaging.

J Biomed Opt

January 2016

University of California, Tu and Yuen Center for Functional Onco-Imaging, Department of Radiological Sciences, 164 Irvine Hall, Irvine, California, United States.

We present experimental results that validate our imaging technique termed photomagnetic imaging (PMI). PMI illuminates the medium under investigation with a near-infrared light and measures the induced temperature increase using magnetic resonance imaging. A multiphysics solver combining light and heat propagation is used to model spatiotemporal distribution of temperature increase.

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Trimodal color-fluorescence-polarization endoscopy aided by a tumor selective molecular probe accurately detects flat lesions in colitis-associated cancer.

J Biomed Opt

December 2014

Washington University in St. Louis, Department of Radiology, 4525 Scott Avenue, East Building, St. Louis, Missouri 63110, United StatesbWashington University in St. Louis, Department of Biomedical Engineering, 1 Brookings Drive, St. Louis, Missouri 63110.

Colitis-associated cancer (CAC) arises from premalignant flat lesions of the colon, which are difficult to detect with current endoscopic screening approaches. We have developed a complementary fluorescence and polarization reporting strategy that combines the unique biochemical and physical properties of dysplasia and cancer for real-time detection of these lesions. Using azoxymethane-dextran sodium sulfate (AOM-DSS) treated mice, which recapitulates human CAC and dysplasia, we show that an octapeptide labeled with a near-infrared (NIR) fluorescent dye selectively identified all precancerous and cancerous lesions.

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