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首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Development of Ga-68 labeled, biotinylated thiosemicarbazone dextran-coated iron oxide nanoparticles as multimodal PET/MRI probe
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Development of Ga-68 labeled, biotinylated thiosemicarbazone dextran-coated iron oxide nanoparticles as multimodal PET/MRI probe

机译:Ga-68的研制标记为生物素化硫代术毒酮的葡聚糖涂层氧化铁纳米粒子作为多模式PET / MRI探针

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Bifunctional biotinylated thiosemicarbazone dextran-coated iron oxide Nanoparticles (NPs) were fabricated. Aldehyde groups of the oxidized dextran-coating layer were utilized to conjugate biotin as a tumor-targeting agent and thiosemicarbazide as a cation chelator on the surface of NPs. The final product was characterized for physicochemical and biological properties. It was compatible with red blood cells and did not change the blood coagulation time. It also showed a significantly enhanced affinity to biotin receptor-positive 4T1 cells compared to non-biotinylated ones. The r2 relaxivity coefficient value of the final product was 110.2 mM(-1) s(-1). Although biotinylated NPs were easily radiolabeled with Ga-68 at room temperature, the stable radiolabeled NPs were achieved at a higher temperature (60 degrees C). The radiolabeled NPs were majorly accumulated in the liver and spleen. However, about 5.4% ID/g of the radiolabeled NPs was accumulated within the 4T1 tumor site. Blocking studies was performed by the biotin molecules pre-injection showed uptake reduction in the 4T1 tumor (about 1.1% ID/g). The radiolabeled NPs could be used for the early detection of biotin receptor-positive tumors via PET-MRI. (C) 2020 Elsevier B.V. All rights reserved.
机译:制造双官能生物素化的硫代吡啶脱氧化铁涂层氧化铁纳米颗粒(NPS)。将氧化葡聚糖涂层层的醛基用于将生物素缀合物作为肿瘤靶向剂和硫代氧化氮杂物作为NPS表面的阳离子螯合剂。最终产物的特征在于物理化学和生物学性质。它与红细胞相容,并没有改变血液凝固时间。与非生物素化的含量相比,它还显示出对生物素受体阳性4T1细胞的显着增强的亲和力。最终产品的R2松弛率系数值为110.2mm(-1)s(-1)。尽管在室温下,生物素化的NPS在Ga-68中易于放射起来,但在较高的温度(60℃)下达到稳定的放射性标记的NP。放射性标记的NPS在肝脏和脾脏中主要积累。然而,在4T1肿瘤部位内积累了约5.4%的放射性标记NPS。通过生物素分子预注射进行阻断研究显示4T1肿瘤的摄取降低(约1.1%ID / g)。放射性标记的NPS可用于通过PET-MRI早期检测生物素受体阳性肿瘤。 (c)2020 Elsevier B.v.保留所有权利。

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