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Maximizing the Relaxivity of Gd-Complex by Synergistic Effect of HSA and Carboxylfullerene

机译:通过HSA和羧基富勒烯的协同效应使Gd复合物的弛豫度最大化

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Macromolecular magnetic resonance imaging (MRI) contrast agent Gd-DTPA-HSA (DTPA, diethylene triamine pentacetate acid; HSA, human serum albumin) as a model has been successfully conjugated with trimalonic acid modified C_(60) for contrast enhancement at clinically used magnetic field strength. The Gd-DTPA-HSA-C_(60) conjugate exhibit maximal relaxivity (r1 - 86 mM~(-1) s~(-1) at 0.5 T, 300 K) reported so far, which is much superior to that of the control Gd-DTPA-HSA (r1 = 38 mM~(-1) s~(-1)) under the same condition and comparable to the theoretical maximum (r1 = 80-120 mM~(-1) s~(-1), at 20 MHz and 298 K), indicating the synergistic effect of HSA and carboxylfullerene on the increased contrast enhancement. TEM characterization reveals that both Gd-DTPA-HSA-C_(60) and Gd-DTPA-HSA can penetrate the cells via endocytosis and transmembrane, respectively, suggesting the potential to sensitively image the events at the cellular and subcellular levels. In addition, the fusion of fullerene with Gd-DTPA-HSA will further endow the resulting complex with photodynamic therapy (PDT) property and thus combine the modalities of therapy (PDT) and diagnostic imaging (MRI) into one entity. More importantly, the payloaded Gd-DTPA may substitute for other more stable Gd-DOTA and HSA as a theranostic package can further work as a drug delivery carrier and effectively control drug release through proteolysis.
机译:大分子磁共振成像(MRI)造影剂Gd-DTPA-HSA(DTPA,二亚乙基三胺五乙酸; HSA,人血清白蛋白)作为模型已成功地与均苯三酸修饰的C_(60)结合,以增强临床使用的磁性对比场强。迄今为止报道的Gd-DTPA-HSA-C_(60)共轭物表现出最大的弛豫性(在0.5 T,300 K时r1-86 mM〜(-1)s〜(-1)),远远优于在相同条件下并与理论最大值相当(r1 = 80-120 mM〜(-1)s〜(-1)时,控制Gd-DTPA-HSA(r1 = 38 mM〜(-1)s〜(-1)) ),在20 MHz和298 K),表明HSA和羧基富勒烯对增强的对比度增强具有协同作用。 TEM表征显示,Gd-DTPA-HSA-C_(60)和Gd-DTPA-HSA均可分别通过内吞作用和跨膜穿透细胞,这表明在细胞和亚细胞水平上敏感地成像事件的潜力。此外,富勒烯与Gd-DTPA-HSA的融合将进一步使所得复合物具有光动力疗法(PDT)的特性,从而将疗法(PDT)和诊断成像(MRI)的方式结合在一起。更重要的是,有效载荷的Gd-DTPA可以替代其他更稳定的Gd-DOTA和HSA,因为治疗试剂盒可以进一步充当药物输送载体,并通过蛋白水解有效地控制药物释放。

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