石墨烯及氧化石墨烯药物递送系统中阿霉素pH依赖性扩散、负载与释放的分子模拟
Molecular simulation of pH-dependent diffusion, loading, and release of doxorubicin in graphene and graphene oxide drug delivery systems.
作者信息
Mahdavi Mina, Rahmani Farzin, Nouranian Sasan
机构信息
Department of Chemical Engineering, The University of Mississippi, University, MS 38677, USA.
出版信息
J Mater Chem B. 2016 Dec 14;4(46):7441-7451. doi: 10.1039/c6tb00746e. Epub 2016 Nov 10.
In this study, the adsorption of doxorubicin (DOX), an anticancer drug, on pristine graphene (PG) and graphene oxide (GO) nanocarriers with different surface oxygen densities and in an aqueous environment with varying pH levels was investigated using molecular dynamics (MD) simulation. The drug loading and release on the GO nanocarrier was also simulated using pH as the controller mechanism. Overall, the DOX/nanocarrier interactions become stronger as the graphene surface oxygen density increases. Although pH has a negligible effect on the single-molecule drug adsorption on the GO surfaces under acidic and neutral conditions, significantly stronger DOX/nanocarrier interactions occur for the GO nanosheet with a lower surface oxygen density (GO-16, with an O/C ratio of 1 : 6) at basic pH levels. Moreover, the DOX/nanocarrier interactions are greatly weakened in the GO nanosheet with higher surface oxygen density (GO-13, with an O/C ratio of 1 : 3) under basic conditions. These observations are partly attributed to a more favorable geometry of the DOX molecule on the GO-16 surface as opposed to a loosely attached DOX molecule on the edges of the GO-13 nanosheet. When comparing the adsorption kinetics and transport properties of the DOX molecule in different GO systems, the drug diffusion coefficient increases with decreasing pH value (going from basic to neutral to acidic) due to the reduced total water-nanocarrier interactions. The latter observation is an indication of the more facilitated transport of the DOX molecule in an aqueous medium towards the nanocarrier surface at lower pH levels. Finally, we have confirmed the loading and release of the DOX molecules on the GO nanocarrier under neutral (pH = 7) and acidic (pH = 5) conditions, respectively. The former signifies the blood pH level, whereas the latter is reminiscent of the pH of a tumorous cell. The computational results presented in this work reveal the underlying mechanisms of DOX loading and release on PG and GO surfaces, which may be used to design better graphene-based nanocarriers for the DOX delivery and targeting applications.
在本研究中,使用分子动力学(MD)模拟研究了抗癌药物阿霉素(DOX)在具有不同表面氧密度的原始石墨烯(PG)和氧化石墨烯(GO)纳米载体上以及在不同pH值的水性环境中的吸附情况。还以pH作为控制机制模拟了DOX在GO纳米载体上的负载和释放。总体而言,随着石墨烯表面氧密度的增加,DOX/纳米载体相互作用变强。尽管在酸性和中性条件下,pH对GO表面上单分子药物吸附的影响可忽略不计,但在碱性pH水平下,对于表面氧密度较低的GO纳米片(GO-16,O/C比为1∶6),DOX/纳米载体相互作用明显更强。此外,在碱性条件下,表面氧密度较高的GO纳米片(GO-13,O/C比为1∶3)中DOX/纳米载体相互作用大大减弱。这些观察结果部分归因于DOX分子在GO-16表面上具有更有利的几何形状,而不是在GO-13纳米片边缘上松散附着的DOX分子。在比较不同GO系统中DOX分子的吸附动力学和传输性质时,由于总的水-纳米载体相互作用减少,药物扩散系数随pH值降低(从碱性到中性再到酸性)而增加。后一观察结果表明,在较低pH水平下,DOX分子在水性介质中向纳米载体表面的传输更容易。最后,我们分别证实了DOX分子在中性(pH = 7)和酸性(pH = 5)条件下在GO纳米载体上的负载和释放。前者代表血液pH水平,而后者使人联想到肿瘤细胞的pH。这项工作中给出的计算结果揭示了DOX在PG和GO表面上负载和释放的潜在机制,这可用于设计更好的基于石墨烯的纳米载体,用于DOX递送和靶向应用。