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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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    Wrapping of nanoparticles by the cell membrane: the role of interactions between the nanoparticles

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    论文类型:期刊论文

    发表时间:2015-11-28

    发表刊物:SOFT MATTER

    收录刊物:SCIE、EI、PubMed、Scopus

    卷号:11

    期号:44

    页面范围:8674-8683

    ISSN号:1744-683X

    摘要:A fundamental understanding of the interactions between nanoparticles (NPs) and the cell membrane is essential to improve the performance of the NP-based biomedical applications and assess the potential toxicity of NPs. Despite the great progress in understanding the interaction between individual NP and the membrane, little is known about the interaction between multiple NPs and the membrane. In this work, we investigate the wrapping of two parallel elongated NPs by the membrane, taking the NP-NP electrostatic interaction and van der Waals (vdW) interaction into consideration. Three types of NPs, namely the rigid NPs with circular and elliptic cross-sections and the deformable NPs, are systematically investigated. The results show that the electrostatic interaction would enhance the tendency of the independent wrapping and inhibit the rotation of the elongated and equally charged NPs with elliptic cross-sections. Under the vdW interaction, the competition of the NP-NP adhesion and the membrane elastic energies with the NP-membrane adhesion energy leads the NPs to be wrapped cooperatively or independently. For the system with elongated NPs with elliptic cross-sections, the NPs are more likely to be wrapped independently as the shapes become more anisotropic and the NPs would rotate to contact each other with the flat sides in the cooperative wrapping configuration. Moreover, the soft NPs are more likely to be wrapped cooperatively compared with the stiff NPs. These results may provide guidelines to control the internalization pathway of NPs and improve the efficiency of NP-based drug delivery systems.