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Nanomedicine ; 32: 102330, 2021 02.
Artigo em Inglês | MEDLINE | ID: mdl-33171287

RESUMO

Active foamy macrophage enrichment drives atherosclerotic plaque initiation and evolution, and is the prominent target for precisely identifying vulnerable plaque. Precise imaging of high-risk plaque allows promotion of treatment and prevention of vascular pathema. However, current iron oxide (IO) nanoparticles-based magnetic resonance (MR) imaging of plaque is often limited by insufficient perfusion and nonspecific accumulation of peri-aortic lymph nodes. Besides that, intrinsic defects of MR also impede its use for accurately identifying plaque details. Herein, by conjugating with PP1 peptide, a novel magnetic mesoporous silica nanoparticle (PIMI) loaded with near-infrared fluorescence (NIRF) dye (IR820) was fabricated to specifically target and quantify macrophage enrichment of atherosclerotic plaque in ApoE-/- mice using dual MR/NIRF imaging. Biocompatibility experiments ulteriorly confirmed the high safety of PIMI nanoparticles in vivo, which lays the foundation of next-generation contrast agent for recognizing macrophage-rich plaque in the near future.


Assuntos
Macrófagos/metabolismo , Imageamento por Ressonância Magnética , Nanopartículas de Magnetita/química , Placa Aterosclerótica/patologia , Dióxido de Silício/química , Animais , Aorta/patologia , Materiais Biocompatíveis/química , Morte Celular , Sobrevivência Celular , Fluorescência , Nanopartículas de Magnetita/ultraestrutura , Camundongos , Células RAW 264.7 , Receptores Depuradores Classe A/metabolismo
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