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1.
Bioconjug Chem ; 23(3): 372-81, 2012 Mar 21.
Article in English | MEDLINE | ID: mdl-22304718

ABSTRACT

Combining various imaging modalities often leads to complementary information and synergistic advantages. A trimodal long-circulating imaging agent tagged with radioactive, magnetic resonance, and fluorescence markers is able to combine the high sensitivity of SPECT with the high resolution of MRI over hours and days. The fluorescence marker helps to confirm the in vivo imaging information at the microscopic level, in the context of the tumor microenvironment. To make a trimodal long-circulating probe, high-molecular-weight hyperbranched polyglycerols (HPG) were modified with a suitable ligand for (111)In radiolabeling and Gd coordination, and additionally tagged with a fluorescent dye. The resulting radiopharmaceutical and contrast agent was nontoxic and hemocompatible. Measured radioactively, its total tumor uptake increased from 2.6% at 24 h to 7.3% at 72 h, which is twice the increase expected due to tumor growth in this time period. Both in vivo MRI and subsequent histological analyses of the same tumors confirmed maximum HPG accumulation at 3 days post injection. Furthermore, Gd-derivatized HPG has an excellent contrast enhancement on T1-weighted MRI at 10× lower molar concentrations than commercially available Galbumin. HPG derivatized with gadolinium, radioactivity, and fluorescence are thus long-circulating macromolecules with great potential for imaging of healthy and leaky blood vessels using overlapping multimodal approaches and for the passive targeting of tumors.


Subject(s)
Biocompatible Materials , Glycerol/metabolism , Neoplasms/metabolism , Polymers/metabolism , Cells, Cultured , Complement Activation , Erythrocytes/cytology , Glycerol/pharmacokinetics , Humans , Polymers/pharmacokinetics , Thrombelastography , Tissue Distribution , Tomography, Emission-Computed, Single-Photon
2.
Int J Pharm ; 422(1-2): 418-27, 2012 Jan 17.
Article in English | MEDLINE | ID: mdl-22044540

ABSTRACT

PURPOSE: Currently, in vivo or in vitro(99m)Tc-radiolabelled red blood cells are the standard blood pool imaging agents. Due to risks associated with handling of blood and the problems with the current (99m)Tc shortage, we were interested in a long-circulating biocompatible synthetic macromolecule that would be simple to prepare and could also be used for PET imaging. METHODS: A high molecular weight hyperbranched polyglycerol (HPG) of 500 kDa was derivatized to coordinate radioactive gallium and to establish its labelling efficiency, stability and pharmacokinetics. RESULTS: The resulting radiopharmaceutical in kit form was labelled rapidly within a couple of minutes at room temperature, was stable in transferrin and EDTA challenge tests, and was non-toxic in both cell viability and different hemocompatibility assays. A pharmacokinetic biodistribution study showed that the (67)Ga-HPGN was confined to the blood compartment with a biological half life of 50.7h. CONCLUSION: (67)Ga-HPGN is thus a simple to prepare blood pool imaging agent for applications where a long biological half-life is essential, i.e., the diagnosis of internal bleeding. Since radiolabelling of the same kit with (68)Ga was also confirmed, we plan to evaluate it shortly as a PET blood pool imaging agent for cardiac applications.


Subject(s)
Gallium Radioisotopes/pharmacokinetics , Gated Blood-Pool Imaging/methods , Glycerol/pharmacokinetics , Polymers/pharmacokinetics , Positron-Emission Tomography , Radiopharmaceuticals/pharmacokinetics , Animals , Blood Coagulation/drug effects , Cell Survival , Cells, Cultured , Complement Activation , Erythrocyte Aggregation/drug effects , Gallium Radioisotopes/administration & dosage , Gallium Radioisotopes/blood , Gallium Radioisotopes/chemistry , Gallium Radioisotopes/toxicity , Glycerol/administration & dosage , Glycerol/blood , Glycerol/chemistry , Glycerol/toxicity , Half-Life , Human Umbilical Vein Endothelial Cells/drug effects , Human Umbilical Vein Endothelial Cells/pathology , Humans , Injections, Intravenous , Molecular Structure , Molecular Weight , Partial Thromboplastin Time , Platelet Activation/drug effects , Polymers/administration & dosage , Polymers/chemistry , Polymers/toxicity , Prothrombin Time , Radiopharmaceuticals/administration & dosage , Radiopharmaceuticals/blood , Radiopharmaceuticals/chemistry , Radiopharmaceuticals/toxicity , Rats , Rats, Sprague-Dawley , Thrombelastography , Tissue Distribution
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