Department of Engineering Science and Mechanics, Virginia Tech, Blacksburg, VA 24061, USA.
Soft Matter. 2013 Dec 28;9(48):11645-9. doi: 10.1039/c3sm52126e.
The drug delivery admissibility of nanomaterials such as carbon nanotubes and their uncertain interactions with live tissues and organs have sparked ongoing research efforts. To boost the selective diffusivity of single walled carbon nanotubes (SWCNTs), surface functionalization was adopted in several experimental attempts. Numerous studies had identified polyethylene glycol (PEG) as a bio-compatible surfactant to carbon nanotubes. In this study, a large scale, atomistic molecular dynamic simulation was utilized to disclose the cellular exposure and uptake mechanisms of PEG-functionalized single walled carbon nanotubes (f-SWCNTs) into a lipid bilayer cell membrane. Results showed that with PEGs attached to a SWCNT, the penetration depth and speed can be controlled. Also, the simulations revealed that the adhesion energy between the nanotube and the lipid membrane is affected considerably, in the presence of PEGs, by the chirality of the SWCNTs.
纳米材料(如碳纳米管)的药物输送可接受性及其与活组织和器官的不确定相互作用引起了正在进行的研究工作。为了提高单壁碳纳米管(SWCNT)的选择性扩散率,在一些实验尝试中采用了表面功能化。许多研究已经确定聚乙二醇(PEG)是碳纳米管的生物相容表面活性剂。在这项研究中,利用大规模原子分子动力学模拟揭示了 PEG 功能化单壁碳纳米管(f-SWCNT)进入脂质双层细胞膜的细胞暴露和摄取机制。结果表明,通过将 PEG 附着到 SWCNT 上,可以控制穿透深度和速度。此外,模拟还表明,在存在 PEG 的情况下,SWCNT 的手性对纳米管与脂质膜之间的粘附能有很大影响。