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1.
J Histochem Cytochem ; 61(1): 19-30, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23092790

ABSTRACT

The ability to visualize myelin is important in the diagnosis of demyelinating disorders and the detection of myelin-containing nerves during surgery. The development of myelin-selective imaging agents requires that a defined target for these agents be identified and that a robust assay against the target be developed to allow for assessment of structure-activity relationships. We describe an immunohistochemical analysis and a fluorescence polarization binding assay using purified myelin basic protein (MBP) that provides quantitative evidence that MBP is the molecular binding partner of previously described myelin-selective fluorescent dyes such as BMB, GE3082, and GE3111.


Subject(s)
Myelin Basic Protein/metabolism , Aniline Compounds , Animals , Corpus Striatum/metabolism , Fluorescence Polarization , Fluorescent Dyes , Immunohistochemistry , Ligands , Mice , Myelin Basic Protein/chemistry , Protein Binding , Stilbenes , Sulfonamides , Trigeminal Nerve/metabolism
2.
Mol Imaging Biol ; 14(6): 708-17, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22488576

ABSTRACT

PURPOSE: Patients suffer from complications as a result of unintentional nerve damage during surgery. We focus on improving intraoperative visualization of nerves through the use of a targeted fluorophore and optical imaging instrumentation. PROCEDURE: A myelin-targeting fluorophore, GE3111, was synthesized, characterized for its optical and myelin-binding properties using purified myelin basic protein, and evaluated in mice. Additionally, a compact instrument was adapted to visualize nerves. RESULTS: GE3111 was synthesized using a versatile methodology. Its optical properties were sensitive to the local environment both in vitro and in vivo. Following intravenous injection, central and peripheral nerves were visualized, with the kinetics of nerve uptake modifiable depending on the formulation. Fluorescence polarization showed specific and strong binding to purified myelin basic protein. Nerves were visualized in vivo using a dedicated compact imaging device requiring less than 2.5 mW/cm(2) of illumination at 405 nm. CONCLUSIONS: Fluorescence imaging of nerves through myelin showed a potential for use in image-guided surgery. Intraoperative nerve imaging is an example where contrast agent and instrument development come together as a result of clinical need.


Subject(s)
Aniline Compounds , Contrast Media , Diagnostic Imaging/methods , Myelin Sheath/pathology , Peripheral Nerves/pathology , Sulfonamides , Administration, Intravenous , Aniline Compounds/chemical synthesis , Aniline Compounds/chemistry , Aniline Compounds/pharmacokinetics , Animals , Cattle , Contrast Media/chemical synthesis , Contrast Media/chemistry , Contrast Media/pharmacokinetics , Dose-Response Relationship, Drug , Intraoperative Period , Male , Mice , Myelin Basic Protein/metabolism , Optical Phenomena , Organ Specificity , Solvents/chemistry , Spectrometry, Fluorescence , Sulfonamides/chemical synthesis , Sulfonamides/chemistry , Sulfonamides/pharmacokinetics , Surgery, Computer-Assisted
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