Methods using fluorescent probes to identify cancer signatures and biological activities of cancer cells hold great promise. Probes based on fluorescence resonance energy transfer (FRET) and techniques such as fluorescence correlation spectroscopy (FCS) and other similar technologies offer the ability to identify specific RNA or protein molecules that can identify a cancer and provide information on oncogenic pathways used by the tumor cells. Other probes can give insight into drug response by measuring apoptosis induction by chemotherapies and radiation. However, fluorescent analysis has several limitations. Most ex vivo analyses use a flow cytometer or complex, confocal microscope to perform analyses, and this requires that tissue be removed from the body and often disrupted into cells, then fixed and analyzed in a static manner. The problems with in vivo fluorescent analysis are even greater since background fluorescence and tissue scattering, even in the near-infrared range, limit signal acquisition to the skin. Two-photon excitation has been a critical advance in optics, facilitating FRET, FCS and CARS techniques in vitro. However, these applications are limited by the complex technology (confocal microscopy) necessary to employ these techniques. We have demonstrated the use of two-photon fluorescence analysis through optical fibers for analysis of cancer cells in vitro and human tumors in vivo in SCID mice. This prior work constitutes the equivalent of an R21 proposal, as we achieved our major objectives: to develop sensing system optics and electronics and to document the ability of this system to obtain and analyze fluorescence signals in vitro and in vivo. The primary goal of this R33 application is to develop a more sensitive prototype device based on a novel dual-clad photonic crystal fiber (DCPCF) that we hypothesize will provide the sensitivity and redundancy necessary for the clinical evaluation of fluorescence signals in vivo using several fluorescence techniques. We plan to carry out our studies in three Specific Aims: ? ? 1: Develop DCPCF for use in a two-photon optical fiber fluorescence probe (D-TPOFF). ? 2: Utilize the D-TPOFF to quantify cancer signatures in vitro and monitor drug effects in tumor cells using targeted nanoparticles ex vivo and in vivo. ? 3: Utilize D-TPOFF to adapt other fluorescent techniques to examine events in tumors in vivo. ? ? At the end of these studies, this technology will be at a point where it is ready for commercialization. ? ?

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Exploratory/Developmental Grants Phase II (R33)
Project #
5R33CA112141-02
Application #
7123836
Study Section
Special Emphasis Panel (ZCA1-SRRB-C (M1))
Program Officer
Baker, Houston
Project Start
2005-09-30
Project End
2008-08-31
Budget Start
2006-09-01
Budget End
2007-08-31
Support Year
2
Fiscal Year
2006
Total Cost
$379,800
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Thomas, Thommey P; Chang, Yu-Chung; Ye, Jing Yong et al. (2012) Optical fiber-based in vivo quantification of growth factor receptors. Cancer 118:2148-56
Thomas, Thommey P; Goonewardena, Sascha N; Majoros, Istvan J et al. (2011) Folate-targeted nanoparticles show efficacy in the treatment of inflammatory arthritis. Arthritis Rheum 63:2671-80
Chang, Yu-Chung; Ye, Jing Yong; Thomas, Thommey P et al. (2010) Fiber-optic multiphoton flow cytometry in whole blood and in vivo. J Biomed Opt 15:047004
Thomas, Thommey P; Shukla, Rameshwer; Kotlyar, Alina et al. (2010) Dendrimer-based tumor cell targeting of fibroblast growth factor-1. Bioorg Med Chem Lett 20:700-3
Chang, Yu-Chung; Ye, Jing Yong; Thomas, Thommey P et al. (2009) Two-photon in vivo flow cytometry using a fiber probe. Proc SPIE Int Soc Opt Eng 7173:71730I1-71730I10
Thomas, Thommey P; Majoros, Istvan; Kotlyar, Alina et al. (2009) Cationic poly(amidoamine) dendrimer induces lysosomal apoptotic pathway at therapeutically relevant concentrations. Biomacromolecules 10:3207-14
Thomas, Thommey P; Ye, Jing Yong; Chang, Yu-Chung et al. (2008) Investigation of tumor cell targeting of a dendrimer nanoparticle using a double-clad optical fiber probe. J Biomed Opt 13:014024
Tkaczyk, Eric R; Mauring, Koit; Tkaczyk, Alan H et al. (2008) Control of the blue fluorescent protein with advanced evolutionary pulse shaping. Biochem Biophys Res Commun 376:733-7
Tkaczyk, Eric R; Zhong, Cheng Frank; Ye, Jing Yong et al. (2008) In Vivo Monitoring of Multiple Circulating Cell Populations Using Two-photon Flow Cytometry. Opt Commun 281:888-894
Chang, Yu-Chung; Ye, Jing Yong; Thomas, Thommey et al. (2008) Two-photon fluorescence correlation spectroscopy through a dual-clad optical fiber. Opt Express 16:12640-9

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