Literature DB >> 17910693

Dual-mode reflectance and fluorescence near-video-rate confocal microscope for architectural, morphological and molecular imaging of tissue.

Alicia L Carlson1, Lezlee G Coghlan, Ann M Gillenwater, Rebecca R Richards-Kortum.   

Abstract

We have developed a near-video-rate dual-mode reflectance and fluorescence confocal microscope for the purpose of imaging ex vivo human specimens and in vivo animal models. The dual-mode confocal microscope (DCM) has light sources at 488, 664 and 784 nm, a frame rate of 15 frames per second, a maximum field of view of 300 x 250 mum and a resolution limit of 0.31 mum laterally and 1.37 mum axially. The DCM can image tissue architecture and cellular morphology, as well as molecular properties of tissue, using reflective and fluorescent molecular-specific optical contrast agents. Images acquired with the DCM demonstrate that the system has the sub-cellular resolution needed to visualize the morphological and molecular changes associated with cancer progression and has the capability to image animal models of disease in vivo. In the hamster cheek pouch model of oral carcinogenesis, the DCM was used to image the epithelium and stroma of the cheek pouch; blood flow was visible and areas of dysplasia could be distinguished from normal epithelium using 6% acetic acid contrast. In human oral cavity tissue slices, DCM reflectance images showed an increase in the nuclear-to-cytoplasmic ratio and density of nuclei in neoplastic tissues as compared to normal tissue. After labelling tissue slices with fluorescent contrast agents targeting the epidermal growth factor receptor, an increase in epidermal growth factor receptor expression was detected in cancerous tissue as compared to normal tissue. The combination of reflectance and fluorescence imaging in a single system allowed imaging of two different parameters involved in neoplastic progression, providing information about both the morphological and molecular expression changes that occur with cancer progression. The dual-mode imaging capabilities of the DCM allow investigation of both morphological changes as well as molecular changes that occur in disease processes. Analyzing both factors simultaneously may be advantageous when trying to detect and diagnose disease. The DCM's high resolution and near-video-rate image acquisition and the growing inventory of molecular-specific contrast agents and disease-specific molecular markers holds significant promise for in vivo studies of disease processes such as carcinogenesis.

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Year:  2007        PMID: 17910693     DOI: 10.1111/j.1365-2818.2007.01818.x

Source DB:  PubMed          Journal:  J Microsc        ISSN: 0022-2720            Impact factor:   1.758


  11 in total

1.  Low-cost, portable optical imaging systems for cancer diagnosis.

Authors:  Mark C Pierce; Rebecca Richards-Kortum
Journal:  Annu Int Conf IEEE Eng Med Biol Soc       Date:  2010

Review 2.  Optical contrast agents and imaging systems for detection and diagnosis of cancer.

Authors:  Mark C Pierce; David J Javier; Rebecca Richards-Kortum
Journal:  Int J Cancer       Date:  2008-11-01       Impact factor: 7.396

3.  Rapid imaging of large tissues using high-resolution stage-scanning microscopy.

Authors:  Tao Yang; Ting Zheng; Zhenhua Shang; Xiaojun Wang; Xiaohua Lv; Jing Yuan; Shaoqun Zeng
Journal:  Biomed Opt Express       Date:  2015-04-23       Impact factor: 3.732

Review 4.  Advances in fluorescence imaging techniques to detect oral cancer and its precursors.

Authors:  Dongsuk Shin; Nadarajah Vigneswaran; Ann Gillenwater; Rebecca Richards-Kortum
Journal:  Future Oncol       Date:  2010-07       Impact factor: 3.404

5.  Imaging inflammation in mouse colon using a rapid stage-scanning confocal fluorescence microscope.

Authors:  Meagan A Saldua; Cory A Olsovsky; Evelyn S Callaway; Robert S Chapkin; Kristen C Maitland
Journal:  J Biomed Opt       Date:  2012-01       Impact factor: 3.170

6.  Molecular imaging of glucose uptake in oral neoplasia following topical application of fluorescently labeled deoxy-glucose.

Authors:  Nitin Nitin; Alicia L Carlson; Tim Muldoon; Adel K El-Naggar; Ann Gillenwater; Rebecca Richards-Kortum
Journal:  Int J Cancer       Date:  2009-06-01       Impact factor: 7.396

7.  Confocal microscopy and molecular-specific optical contrast agents for the detection of oral neoplasia.

Authors:  Alicia L Carlson; Ann M Gillenwater; Michelle D Williams; Adel K El-Naggar; R R Richards-Kortum
Journal:  Technol Cancer Res Treat       Date:  2007-10

8.  High-speed combined reflectance confocal and moxifloxacin based two-photon microscopy.

Authors:  Bumju Kim; Hoan Le; Byung-Ho Oh; Ki Hean Kim
Journal:  Biomed Opt Express       Date:  2020-02-21       Impact factor: 3.732

9.  Quantification of confocal fluorescence microscopy for the detection of cervical intraepithelial neoplasia.

Authors:  Fahime Sheikhzadeh; Rabab K Ward; Anita Carraro; Zhao Yang Chen; Dirk van Niekerk; Dianne Miller; Tom Ehlen; Calum E MacAulay; Michele Follen; Pierre M Lane; Martial Guillaud
Journal:  Biomed Eng Online       Date:  2015-10-24       Impact factor: 2.819

10.  Comparison of Confocal and Super-Resolution Reflectance Imaging of Metal Oxide Nanoparticles.

Authors:  Emily J Guggenheim; Abdullah Khan; Jeremy Pike; Lynne Chang; Iseult Lynch; Joshua Z Rappoport
Journal:  PLoS One       Date:  2016-10-03       Impact factor: 3.240

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