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  • 1
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 72, No. 8_Supplement ( 2012-04-15), p. 4235-4235
    Abstract: The development of novel cancer therapies could benefit significantly from the introduction of new functional imaging methods that allow non-invasive longitudinal assessment of tumor response to therapy. We have developed and tested a new instrument in which photoacoustic (PA) imaging is combined with co-registered micro-ultrasound (µUS). The new system allows tumor oxygenation and hemoglobin data derived from PA imaging to be combined with blood volume and perfusion data derived from contrast µUS and be observed during the course of therapy. Using this system, we assessed changes in the tumor microenvironment following treatment with an anti-angiogenic drug, sunitinib (Pfizer, USA). Human metastatic breast cancer cells (231/LM2-4) were surgically implanted in the mammary fat pads of 4 control and 7 treated female nude SCID mice and were allowed to grow for 10 days prior to initiation of experimental treatment, which consisted of either 4 consecutive daily gavage doses of 120mg/kg sunitinib, or control vehicle. Imaging was performed, using the VevoLAZR (VisualSonics, Canada) integrated µUS/PA system, prior to and following treatment. Tumor volume was quantified with 3D ultrasound imaging using a 40MHz frequency probe. Indices of relative blood volume and perfusion were quantified with non-linear contrast imaging using a 21MHz probe during a 50uL (2x109/mL) intravenous bolus injection of microbubbles (MicroMarker, VisualSonics). Blood oxygen saturation, relative tissue oxygen saturation, and hemoglobin concentration were measured with photoacoustic imaging using an integrated photoacoustic probe with 21MHz ultrasound frequency and tuneable 680-970nm laser optics. Following treatment, we observed significant (p & lt;.05) suppression in tumor growth (-35%) decrease in blood volume (-91%), perfusion (-86%), relative tissue oxygen saturation (-60%), and hemoglobin concentration (-40%) in the sunitinib- relative to control-treated mice. When comparing pre- and post-treatment within the control group, there were increases in tumor volume (+120%), however, interestingly, there were also decreases in perfusion (-52%), blood volume (-22%) and relative tissue oxygen saturation (-31%). When comparing contrast µUS and PA data, there was a strong, moderate, and weaker correlations between relative tissue oxygen saturation and perfusion (R2 = 0.722), relative tissue oxygenation and blood volume (R2 = 0.576), and blood volume and hemoglobin concentration (R2 = 0.294) respectively. This study demonstrates the ability of an integrated PA and µUS imaging system to provide quantitative functional assessment of a preclinical breast cancer model following treatment with sunitinib. The degree to which quantitative correlates such as these are indicative of useful therapeutic response and of prognostic value remain to be investigated. Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 103rd Annual Meeting of the American Association for Cancer Research; 2012 Mar 31-Apr 4; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2012;72(8 Suppl):Abstract nr 4235. doi:1538-7445.AM2012-4235
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
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    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2012
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  • 2
    Online Resource
    Online Resource
    American Psychological Association (APA) ; 2009
    In:  Behavioral Neuroscience Vol. 123, No. 1 ( 2009), p. 145-155
    In: Behavioral Neuroscience, American Psychological Association (APA), Vol. 123, No. 1 ( 2009), p. 145-155
    Type of Medium: Online Resource
    ISSN: 1939-0084 , 0735-7044
    Language: English
    Publisher: American Psychological Association (APA)
    Publication Date: 2009
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  • 3
    In: The FASEB Journal, Wiley, Vol. 26, No. S1 ( 2012-04)
    Type of Medium: Online Resource
    ISSN: 0892-6638 , 1530-6860
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2012
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    SSG: 12
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  • 4
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2013
    In:  Cancer Research Vol. 73, No. 8_Supplement ( 2013-04-15), p. 3920-3920
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 73, No. 8_Supplement ( 2013-04-15), p. 3920-3920
    Abstract: Photoacoustic imaging is a powerful tool for assessing tumor vasculature and oxygen saturation as well as detecting contrast agents for molecular imaging. Another exciting possibility is to visualize gene expression by using a reporter which produces a photoacoustic contrast agent. Tyrosinase is such a reporter in that its expression results in the production of melanin, which gives a strong photoacoustic signal. Here we describe the use of a commercially available photoacoustic (PA) imaging system (Vevo LAZR, VisualSonics, Toronto) to image inducible gene expression in subcutaneous xenograft tumors using tyrosinase as a reporter gene. The photoacoustic imaging system generated light from a tunable laser (680 - 970 nm) which was delivered through fiber optic bundles integrated into a linear array transducer (LZ-250, fc = 21 MHz), mounted to a linear stepper motor for 3D imaging. Animals (n=3) having MCF-7 xenograft tumors on either flank transfected with (+TYR) or without (-TYR) doxycycline-regulated tyrosinase were imaged before and one week after the induction of tyrosinase expression. 3D images of the tumors were acquired using multiple wavelengths (680, 750, 800, 850, 900 and 950nm) and 2D images were acquired across the entire wavelength range of the laser to generate absorption curves for blood and melanin. To confirm the presence of melanin and distinguish it from the endogenous blood signal, one animal was exsanguinated and the tumor was imaged again. Approximately 1mm-thick slices of the tumors were taken and photographed for visual confirmation of the presence of melanin. Comparison of pre- and post-doxycycline images of +TYR tumors clearly showed enhanced contrast in the tumor which closely matched the absorption spectrum of melanin. This signal persisted upon exsanguination. -TYR tumors showed signal which corresponded with the spectra of oxy and deoxy hemoglobin and changed little over the course of the experiment. Visual inspection of the excised sliced tumors revealed pigmentation in the +TYR tumors which was absent in the -TYR tumors. Here we have shown the ability of the Vevo LAZR photoacoustic imaging system to visualize inducible reporter gene expression in vivo. This has implications for assessing genetically controlled cellular processes and their response to anti-cancer drugs but also for monitoring gene therapy for cancer treatment non-invasively. Citation Format: Andrew Heinmiller, Minalini Lakshman, Dave Bates, Andrew Needles, Catherine Theodoropoulos, Robert J. Paproski, Roger J. Zemp. In vivo tyrosinase reporter gene imaging with multispectral photoacoustic technology. [abstract]. In: Proceedings of the 104th Annual Meeting of the American Association for Cancer Research; 2013 Apr 6-10; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2013;73(8 Suppl):Abstract nr 3920. doi:10.1158/1538-7445.AM2013-3920
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
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    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2013
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  • 5
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 71, No. 8_Supplement ( 2011-04-15), p. 4285-4285
    Abstract: We have developed a photoacoustic (PA) micro-ultrasound imaging system which can be used to image tumour vasculature and derive oxygen saturation measurements from within those vessels. Additionally, the system can be used to detect contrast agents such as methylene blue (MB), which is already used in the clinic to aid in sentinel lymph node detection. Here we describe the assessment of the sensitivity of the system with respect to MB detection and compare oxygen saturation (sO2) measurements derived from our system to expected values. A modified μUS system (Vevo 2100, VisualSonics) was operated with a linear array transducer (MS-250, fc = 21 MHz), retrofitted with a housing that held rectangular fiber optic bundles (25.4 × 1.25 mm) to either side. The rectangular bundles were bifurcated ends of a single bundle that was coupled to a tuneable laser (Rainbow NIR, OPOTEK Inc., Carlsbad CA, 680-970 nm). The μUS system was synchronized with the laser and PA signals were acquired with a fluence & lt; 20 mJ/cm2, beamformed in software, and displayed at 5 Hz. For determination of the sensitivity of the system to MB, serial dilutions of MB were performed (from 3.13E-02 mol/L to 3.13E-08 mol/L) and each dilution was imaged by drawing the solution into a 500 um diameter polyethylene tube. Signal intensity was measured at 680 nm since MB has a peak absorbance around this wavelength, and the minimum detectable concentration was determined. For determination of the presence of MB signal in vivo, PA images of the axillary lymph node were collected at 680 and 760 nm both pre- and post-infusion of MB into the forepaw of an adult CD1 mouse and a subtracted image was generated. Axillary and brachial lymph nodes were excised and imaged to verify the source of the MB signal. sO2 measurements were assessed by imaging the jugular vein of a rat and altering breathed oxygen concentration while simultaneously measuring the oxygen partial pressure (pO2) within the same jugular vein. A real-time parametric sO2 map was generated on the system with a dual wavelength measurement of 750 and 850 nm and sO2 measurements were calculated based on a selected region of interest. Sub-cutaneous tumors were also imaged in 2D and 3D and total haemoglobin and sO2 maps were generated. The minimum detectable concentration of MB was observed to be approximately 520 nM. We were able to see photoacoustic signal generated by MB in the mouse axial lymph node, as well as its afferent lymph vessel, and verify it through excision of the node and subsequent imaging. In vivo contrast enhancement was 16dB at 680 nm. Subtraction of 760 nm from 680 nm data yielded a contrast enhancement improvement of 8-10 dB. In the rat jugular vein, measured sO2 correlated well with expected sO2 values (R2 = 0.832). Within a tumor, PA signal from the vasculature was detected at depths of up to 10mm and total haemoglobin and sO2 measurements were made on these signals. Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 102nd Annual Meeting of the American Association for Cancer Research; 2011 Apr 2-6; Orlando, FL. Philadelphia (PA): AACR; Cancer Res 2011;71(8 Suppl):Abstract nr 4285. doi:10.1158/1538-7445.AM2011-4285
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
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    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2011
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  • 6
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 72, No. 8_Supplement ( 2012-04-15), p. 4338-4338
    Abstract: VisualSonics has recently developed a preclinical photoacoustic (PA) imaging system called the VevoLAZR that combines the sensitivity of optical imaging and the high resolution of micro-ultrasound. The system incorporates a 40 MHz (centre frequency) ultrasound transducer linear array probe (LZ550) and a tuneable 680-970 nm nanosecond pulsed-laser. We used this system to study in vivo changes in tumor oxygen saturation and haemoglobin density caused by exposure to radiation therapy (RT). For this, DsRed-Me180 human cervical tumors were grown in a nude mouse dorsal skinfold window chamber model until they reached 2.5 mm in diameter. Specifically, we investigated the system's sensitivity and dynamic range to measure relative changes in oxygen saturation in tumor and surrounding healthy tissues 10 days after treatment. Tumors (∼2.5 mm diameter) were focally irradiated with a single dose of 30 Gy using a small animal microirradiator (XRAD225, Precision XRay Inc., North Branford, CT). To measure the dynamic range and stability of our setup for measuring oxygen saturation in vivo, we altered the anesthetised animal's inhaled oxygen from 100% to 7% for 1 min during PA imaging. This test showed that blood oxygen saturation in the healthy dorsal skinfold tissue decreased from 82% to 8% and confirmed the linearity of the measurement technique. Furthermore, we compared vascular morphology obtained by photoacoustic imaging and intravital fluorescent microscopy using FITC-Dextran (2 MDa, injected 20 mins prior). This comparison showed good correlation and confirms that PA imaging can provide important structural information of vascularity. Photoacoustic imaging was performed before and 10 days after irradiation to assess changes in tumour volume, relative blood oxygen saturation, relative tissue oxygen saturation, and relative hemoglobin density. Ten days after irradiation, PA imaging showed that the tumour volume increased from 5.7 to 14.2 mm3, relative blood oxygen saturation decreased from 75.3 to 48.2%, relative tissue oxygen saturation decreased from 40.7 to 0.1%, and hemoglobin density decreased from 18457 to 3253 a.u. These data illustrate the capability of PA imaging to simultaneously measure multiple radiobiological response metrics from a single imaging scan. Pilot results demonstrate: i) the compatibility of the VisualSonics small animal VevoLAZR photoacoustic imaging system with intravital murine tumor models, ii) the sensitivity of the system to detect RT-induced changes in tumor vascular oxygen saturation non-invasively, in real time and in vivo, and iii) a new preclinical application of PA imaging for longitudinal monitoring of tumor response to RT in vivo. Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 103rd Annual Meeting of the American Association for Cancer Research; 2012 Mar 31-Apr 4; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2012;72(8 Suppl):Abstract nr 4338. doi:1538-7445.AM2012-4338
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
    RVK:
    RVK:
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2012
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  • 7
    In: The FASEB Journal, Wiley, Vol. 27, No. S1 ( 2013-04)
    Type of Medium: Online Resource
    ISSN: 0892-6638 , 1530-6860
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2013
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    SSG: 12
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  • 8
    In: Ultrasonic Imaging, SAGE Publications, Vol. 41, No. 6 ( 2019-11), p. 319-335
    Abstract: Photoacoustic imaging (PAI) is an emerging biomedical imaging technique that utilizes a combination of light and ultrasound to detect photoabsorbers embedded within tissues. While the clinical utility of PAI has been widely explored for several applications, limitations in light penetration and detector sensitivity have restricted these studies to mostly superficial sites. Given the importance of PA signal generation and detection on light delivery and ultrasound detector frequency, there is an ongoing effort to optimize these parameters to enhance photoabsorber detection at increased depths. With this in mind, in this study we examined performance benchmarks of a commercially available PAI/ultrasound linear array system when using different imaging frequencies and light delivery schemes. A modified light fiber jacket providing focused light delivery (FLD) at the center of the probe was compared with the built-in fiber optics lining the length of the probe. Studies were performed in vitro to compare performance characteristics such as imaging resolution, maximum imaging depth, and sensitivity to varying hematocrit concentration for each frequency and light delivery method. Monte Carlo simulations of each light delivery method revealed increased light penetration with FLD. In tissue-mimicking phantoms, vascular channels used to simulate blood vessels could be visualized at a depth of 2.4 cm when lowering imaging frequency and utilizing FLD. Imaging at lower frequencies with FLD also enabled enhanced detection of varying hematocrit concentration levels at increased depths, although lateral imaging resolution was reduced. Finally, a proof of concept in vivo probe comparison study in a mouse tumor model provided supportive evidence of our in vitro results. Collectively, our findings show that adjusting imaging frequency and applying FLD can be a straightforward approach for improving PAI performance.
    Type of Medium: Online Resource
    ISSN: 0161-7346 , 1096-0910
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2019
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  • 9
    Online Resource
    Online Resource
    SPIE-Intl Soc Optical Eng ; 2017
    In:  Journal of Biomedical Optics Vol. 22, No. 10 ( 2017-10-11), p. 1-
    In: Journal of Biomedical Optics, SPIE-Intl Soc Optical Eng, Vol. 22, No. 10 ( 2017-10-11), p. 1-
    Type of Medium: Online Resource
    ISSN: 1083-3668
    Language: Unknown
    Publisher: SPIE-Intl Soc Optical Eng
    Publication Date: 2017
    detail.hit.zdb_id: 2001934-8
    SSG: 12
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  • 10
    In: Stroke, Ovid Technologies (Wolters Kluwer Health), Vol. 46, No. 7 ( 2015-07), p. 1947-1955
    Abstract: Hypoperfusion-induced thrombosis is an important mechanism for postsurgery stroke and cognitive decline, but there are no perioperative neuroprotectants to date. This study investigated whether prophylactic application of Edaravone, a free radical scavenger already used in treating ischemic stroke in Japan, can prevent infarct and cognitive deficits in a murine model of transient cerebral hypoxia-ischemia. Methods— Adult male C57BL/6 mice were subjected to transient hypoxic-ischemic (tHI) insult that consists of 30-minute occlusion of the unilateral common carotid artery and exposure to 7.5% oxygen. Edaravone or saline was prophylactically applied to compare their effects on cortical oxygen saturation, blood flow, coagulation, oxidative stress, metabolites, and learning-memory using methods that include photoacoustic imaging, laser speckle contrast imaging, solid-state NMR, and Morris water maze. The effects on infarct size by Edaravone application at different time points after tHI were also compared. Results— Prophylactic administration of Edaravone (4.5 mg/kg×2, IP, 1 hour before and 1 hour after tHI) improved vascular reperfusion, oxygen saturation, and the maintenance of brain metabolites, reducing oxidative stress, thrombosis, white-matter injury, and learning impairment after tHI insult. Delayed Edaravone treatment after 3 h post-tHI became unable to reduce infarct size. Conclusions— Acute application of Edaravone may be a useful strategy to prevent postsurgery stroke and cognitive impairment, especially in patients with severe carotid stenosis.
    Type of Medium: Online Resource
    ISSN: 0039-2499 , 1524-4628
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    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2015
    detail.hit.zdb_id: 1467823-8
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