CNRS, Institut de Biologie Moléculaire et Cellulaire, Laboratoire d'Immunopathologie et Chimie Thérapeutique, 67000, Strasbourg, France.
ISIS & icFRC, Université de Strasbourg & CNRS, 8 allée Gaspard Monge, 67000, Strasbourg, France.
Small. 2015 Aug 26;11(32):3985-94. doi: 10.1002/smll.201500038. Epub 2015 May 8.
Understanding human health risk associated with the rapidly emerging graphene-based nanomaterials represents a great challenge because of the diversity of applications and the wide range of possible ways of exposure to this type of materials. Herein, the biodegradation of graphene oxide (GO) sheets is reported by using myeloperoxidase (hMPO) derived from human neutrophils in the presence of a low concentration of hydrogen peroxide. The degradation capability of the enzyme on three different GO samples containing different degree of oxidation on their graphenic lattice, leading to a variable dispersibility in aqueous media is compared. hMPO fails in degrading the most aggregated GO, but succeeds to completely metabolize highly dispersed GO samples. The spectroscopy and microscopy analyses provide unambiguous evidence for the key roles played by hydrophilicity, negative surface charge, and colloidal stability of the aqueous GO in their biodegradation by hMPO catalysis.
理解与快速发展的基于石墨烯的纳米材料相关的人类健康风险是一项巨大的挑战,因为这类材料的应用多样性和可能的暴露方式范围很广。在此,本文报道了在低浓度过氧化氢存在的情况下,利用来源于人中性粒细胞的髓过氧化物酶(hMPO)对氧化石墨烯(GO)片进行生物降解。比较了酶对三种不同 GO 样品的降解能力,这三种 GO 样品在其石墨晶格上具有不同程度的氧化,导致在水介质中的分散性不同。hMPO 不能降解最聚集的 GO,但成功地完全代谢了高度分散的 GO 样品。光谱和显微镜分析为 hMPO 催化作用下水相 GO 的亲水性、负表面电荷和胶体稳定性在其生物降解中所起的关键作用提供了明确的证据。