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1.
Bioconjug Chem ; 23(3): 372-81, 2012 Mar 21.
Artigo em Inglês | MEDLINE | ID: mdl-22304718

RESUMO

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.


Assuntos
Materiais Biocompatíveis , Glicerol/metabolismo , Neoplasias/metabolismo , Polímeros/metabolismo , Células Cultivadas , Ativação do Complemento , Eritrócitos/citologia , Glicerol/farmacocinética , Humanos , Polímeros/farmacocinética , Tromboelastografia , Distribuição Tecidual , Tomografia Computadorizada de Emissão de Fóton Único
2.
Int J Pharm ; 422(1-2): 418-27, 2012 Jan 17.
Artigo em Inglês | MEDLINE | ID: mdl-22044540

RESUMO

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.


Assuntos
Radioisótopos de Gálio/farmacocinética , Imagem do Acúmulo Cardíaco de Comporta/métodos , Glicerol/farmacocinética , Polímeros/farmacocinética , Tomografia por Emissão de Pósitrons , Compostos Radiofarmacêuticos/farmacocinética , Animais , Coagulação Sanguínea/efeitos dos fármacos , Sobrevivência Celular , Células Cultivadas , Ativação do Complemento , Agregação Eritrocítica/efeitos dos fármacos , Radioisótopos de Gálio/administração & dosagem , Radioisótopos de Gálio/sangue , Radioisótopos de Gálio/química , Radioisótopos de Gálio/toxicidade , Glicerol/administração & dosagem , Glicerol/sangue , Glicerol/química , Glicerol/toxicidade , Meia-Vida , Células Endoteliais da Veia Umbilical Humana/efeitos dos fármacos , Células Endoteliais da Veia Umbilical Humana/patologia , Humanos , Injeções Intravenosas , Estrutura Molecular , Peso Molecular , Tempo de Tromboplastina Parcial , Ativação Plaquetária/efeitos dos fármacos , Polímeros/administração & dosagem , Polímeros/química , Polímeros/toxicidade , Tempo de Protrombina , Compostos Radiofarmacêuticos/administração & dosagem , Compostos Radiofarmacêuticos/sangue , Compostos Radiofarmacêuticos/química , Compostos Radiofarmacêuticos/toxicidade , Ratos , Ratos Sprague-Dawley , Tromboelastografia , Distribuição Tecidual
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