Fabio Pieretti, Alessandro Moretto, Emanuele Papini, R. Tavano
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引用次数: 0
Abstract
Graphene oxide (GO) nanoparticles, due to their favorable water solubility, compared to graphene (GA), are a hot research topic in biomedical and pharmaceutical research. However, GO clinical translation may be complicated by its high surface/volume ratio enhancing the interaction with human blood components. In fact, GO’s bi-dimensional nature and strong negative charge may lead to severe biological effects, such as thrombogenicity and immune cell activation. This study explores the impact of further GO surface chemical modulation on major adverse effects: blood plasma coagulation and hemolysis. To this aim, we refined GO nanoparticles by fine-tuned reduction chemistry, esterification and introduction of negative or positive charges. With this approach, we were able to mitigate plasma coagulation and hemolysis at variable degrees and to identify GO derivatives with improved biocompatibility. This opens the door to the progress of graphene-based nanotheranostic applications.
与石墨烯(GA)相比,氧化石墨烯(GO)纳米粒子具有良好的水溶性,是生物医学和制药研究领域的热门研究课题。然而,GO 的高表面/体积比会增强与人体血液成分的相互作用,这可能会使其临床转化变得复杂。事实上,GO 的二维性质和强负电荷可能会导致严重的生物效应,如血栓形成和免疫细胞激活。本研究探讨了进一步调节 GO 表面化学性质对血浆凝固和溶血等主要不良反应的影响。为此,我们通过微调还原化学、酯化和引入负电荷或正电荷来改进 GO 纳米粒子。通过这种方法,我们能够在不同程度上缓解血浆凝固和溶血,并确定了具有更好生物相容性的 GO 衍生物。这为基于石墨烯的纳米otheranostic应用的发展打开了大门。