Journal of Labelled Compounds and Radiopharmaceuticals · 1997 · 36 citations · 12 references
MedicineNuclear MedicineOncologyMolecular ImagingOncologic Nuclear MedicineRadiobiologyCellular Responses To HypoxiaOncologic Nuclear ImagingPharmacokinetics Of Anticancer DrugsRadiopharmaceutical DesignRadiotracer DevelopmentTumor ImagingAnimal Disease ModelsHypoxiaHypoxia-induced RadioresistanceHypoxia-mediated RadioresistanceTissue Hypoxia AssessmentTumor Hypoxia ImagingTumor Microenvironment HypoxiaTumor Radiotracer Imaging
Seven second-generation hypoxic markers of the iodinated azomycin nucleoside class have been synthesized and tested for hypoxia marking activity with tumor cells in vitro and in vivo. β-D-lodoazomycin galactoside (IAZG) and β-D-iodoazomycin xylopyranoside (IAZXP) demonstrated superior hypoxia marking properties relative to IAZA because of their higher water solubilities, rapid plasma clearance rates from tumor-bearing mice and maximum tumor/blood (T/B) and tumor/muscle (T/M) ratios. Our studies with animal tumor models show that T/B or T/M ratios of these markers determined by scintigraphy or planar imaging can predict for the relative degree of tumor hypoxia and for tumor radioresistance. © 1997 John Wiley & Sons, Ltd.
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Spectrometric Identification of Organic Compounds
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