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Cytotoxicity of Surface-functionalized Silicon and Germanium Nanoparticles: The Dominant Role of Surface Charges

机译:表面功能化的硅和锗纳米粒子的细胞毒性:表面电荷的主导作用。

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摘要

Although it is hypothesized that surface (like surface charge) and physical characteristics (like particle size) play important roles in cellular interactions of nanoparticles (NPs), a systematic study probing this issue is missing. Hence, a comparative cytotoxicity study quantifying nine different cellular endpoints, was performed with a broad series of monodisperse, well characterized silicon (Si) and germanium (Ge) NPs with various surface functionalizations. Human colonic adenocarcinoma Caco-2 and rat alveolar macrophage NR8383 cells were used, to clarify the toxicity of this series of NPs. The surface coatings on the NPs appeared to dominate the cytotoxicity: the cationic NPs exhibited cytotoxicity, whereas the carboxylic acid-terminated and hydrophilic PEG- or dextran-terminated NPs did not. Within the cationic Si NPs, smaller Si NPs were more toxic than bigger ones. Manganese-doped (1 % Mn) Si NPs did not show any added toxicity, which favors their further development for bioimaging. Iron-doped (1 % Fe) Si NPs showed some added toxicity, which may be due to the leaching of Fe3+ ions from the core. A silica coating seemed to impart toxicity, in line with the reported toxicity of silica. Intracellular mitochondria seem to be a target organ for the toxic NPs since a dose-, surface charge- and size-dependent imbalance of the mitochondrial membrane potential was observed. Such imbalance led to a series of other cellular events for cationic NPs, like decreased mitochondrial membrane potential (ΔΨm) and ATP production, induction of ROS generation, increased cytoplasmic Ca2+ content, production of TNF-α and enhanced caspase-3 activity. Taken together, the results explain the toxicity of Si NPs/Ge NPs largely by their surface characteristics, provide insight in the mode of action underlying the observed cytotoxicity, and give directions on synthesizing biocompatible Si and Ge NPs, as this is crucial for bioimaging and other applications in for example the field of medicine.
机译:尽管假设表面(如表面电荷)和物理特性(如粒度)在纳米颗粒(NP)的细胞相互作用中起重要作用,但仍缺乏系统的研究来探讨这一问题。因此,对一系列具有多种表面功能化的单分散,特征明确的硅(Si)和锗(Ge)NP进行了一系列比较细胞毒性研究,量化了九种不同的细胞终点。使用人类结肠腺癌Caco-2和大鼠肺泡巨噬细胞NR8383细胞来阐明该系列NP的毒性。 NP上的表面涂层似乎是主要的细胞毒性:阳离子NP表现出细胞毒性,而羧酸封端的和亲水性PEG或葡聚糖封端的NP则没有。在阳离子Si NP中,较小的Si NPs的毒性要大于较大的Si NPs。锰掺杂(1%Mn)Si NPs没有表现出任何增加的毒性,这有利于其进一步用于生物成像。铁掺杂的(1%Fe)Si NPs表现出一定的附加毒性,这可能是由于Fe 3 + 离子从芯中浸出所致。二氧化硅涂层似乎具有毒性,与所报道的二氧化硅毒性相符。由于观察到线粒体膜电位的剂量,表面电荷和尺寸依赖性失衡,细胞内线粒体似乎是有毒NP的靶器官。这种失衡导致阳离子NPs发生一系列其他细胞事件,例如线粒体膜电位(ΔΨm)和ATP降低,诱导ROS产生,细胞质Ca 2 + 含量增加,TNF-α产生和增强的caspase-3活性。综上所述,结果主要通过表面特征来解释Si NPs / Ge NPs的毒性,提供了对观察到的细胞毒性的作用方式的见解,并为合成生物相容的Si和Ge NPs提供了指导,因为这对生物成像和成像至关重要其他应用,例如医学领域。

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