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    郑勇刚

    • 教授     博士生导师   硕士生导师
    • 主要任职:力学与航空航天学院副院长
    • 其他任职:工程力学系副主任(分管本科生、研究生培养)
    • 性别:男
    • 毕业院校:大连理工大学
    • 学位:博士
    • 所在单位:力学与航空航天学院
    • 学科:工程力学. 计算力学. 生物与纳米力学
    • 办公地点:一号综合实验楼620B房间
    • 电子邮箱:zhengyg@dlut.edu.cn

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    Penetration of Lipid Membranes by Gold Nanoparticles: Insights into Cellular Uptake, Cytotoxicity, and Their Relationship

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    论文类型:期刊论文

    发表时间:2010-09-01

    发表刊物:ACS NANO

    收录刊物:SCIE、EI、PubMed、ESI高被引论文、Scopus

    卷号:4

    期号:9

    页面范围:5421-5429

    ISSN号:1936-0851

    关键字:AuNPs (gold nanoparticles); lipid bilayer; penetration; membrane disruption; cellular uptake; cytotoxicity

    摘要:Nanoparticle penetration into cell membranes is an interesting phenomenon that may have crucial implications on the nanoparticles' biomedical applications. In this paper, a coarse-grained model for gold nanoparticles (AuNPs) is developed (verified against experimental data available) to simulate their interactions with model lipid membranes. Simulations reveal that AuNPs with different signs and densities of surface charges spontaneously adhere to the bilayer surface or penetrate into the bilayer interior. The potential of mean force calculations show that the energy gains upon adhesion or penetration is significant. In the case of penetration, it is found that defective areas are induced across the entire surface of the upper leaflet of the bilayer and a hydrophilic pore that transports water molecules was formed with its surrounding lipids highly disordered. Penetration and its concomitant membrane disruptions can be a possible mechanism of the two observed phenomena in experiments: AuNPs bypass endocytosis during their internalization into cells and cytotoxicity of AuNPs. It is also found that both the level of penetration and membrane disruption increase as the charge density of the AuNP increases, but in different manners. The findings suggest a way of controlling the AuNP-cell interactions by manipulating surface charge densities of AuNPs to achieve designated goals in their biomedical applications, such as striking a balance between their cellular uptake and cytotoxicity in order to achieve optimal delivery efficiency as delivery agents.