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In Vivo Biodistribution and Toxicity of Highly Soluble PEG-Coated Boron Nitride in Mice

机译:小鼠体内高可溶性PEG包覆的氮化硼的体内生物分布和毒性

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The boron nitride (BN) nanoparticles, as the structural analogues of graphene, are the potential biomedicine materials because of the excellent biocompatibility, but their solubility and biosafety are the biggest obstacle for the clinic application. Here, we first synthesized the highly soluble BN nanoparticles coated by PEG (BN-PEG) with smaller size (~10?nm), then studied their biodistribution in vivo through radioisotope (Tc_(99m)O~(4) _(?)) labeling, and the results showed that BN-PEG nanoparticles mainly accumulated in the liver, lung, and spleen with the less uptake by the brain. Moreover, the pathological changes induced by BN-PEG could be significantly observed in the sections of the liver, lung, spleen, and heart, which can be also supported by the test of biochemical indexes in serum. More importantly, we first observed the biodistribution of BN-PEG in the heart tissues with high toxicity, which would give a warning about the cardiovascular disease, and provide some opportunities for the drug delivery and treatment.
机译:氮化硼(BN)纳米粒子作为石墨烯的结构类似物,由于其优异的生物相容性而成为潜在的生物医学材料,但其溶解性和生物安全性是临床应用的最大障碍。在这里,我们首先合成了尺寸较小(〜10?nm)的被PEG包覆的高可溶性BN纳米颗粒(BN-PEG),然后通过放射性同位素(Tc_(99m)O〜(4)_(?)标记),结果表明BN-PEG纳米颗粒主要聚集在肝,肺和脾脏中,而大脑吸收较少。此外,BN-PEG诱导的病理变化可以在肝,肺,脾和心脏的切片中明显观察到,这也可以通过检测血清中的生化指标来支持。更重要的是,我们首先观察到BN-PEG在高毒性心脏组织中的生物分布,这将对心血管疾病发出警告,并为药物的输送和治疗提供一些机会。

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