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理解硼氮纳米片和黑磷纳米片作为高效药物传递系统的双重递药:阿霉素和紫杉醇的联合递送。

Understanding dual delivery of doxorubicin and paclitaxel with boron nitride and phosphorene nanosheets as highly efficient drug delivery systems.

机构信息

Department of Chemistry, University of Birjand, Birjand, Iran.

出版信息

J Biomol Struct Dyn. 2021 Sep;39(15):5613-5618. doi: 10.1080/07391102.2020.1794968. Epub 2020 Jul 16.

Abstract

Dual delivery of Doxorubicin (DOX) and Paclitaxel (PTX) anticancer drug molecules with boron nitride (BN) and phosphorene (PH) nanosheets are investigated using molecular dynamics (MD) simulation. Several quantities are employed to examine the adsorption mechanism of DOX and PTX on the carriers. The obtained results indicate that the drug molecules spontaneously move toward the carriers and form stable complexes. In the interaction of the drugs and BN, the contribution of van der Walls (vdW) is higher than electrostatic energy which can be related to the formation of strong π-π interactions between the drugs and the carrier. Moreover, in the same manner, in the adsorption of drugs on the PH surface, the role of vdW interaction is more than electrostatic energy. Moreover, the oxidative properties of BN and PH nanosheets are examined. The obtained results indicated that the diffusion coefficient values of PTX and DOX molecules in the presence of hydroxyl groups are increased, which can attribute to the blocking effect of functional groups.Communicated by Ramaswamy H. Sarma.

摘要

采用分子动力学(MD)模拟研究了 BN 和磷烯(PH)纳米片对阿霉素(DOX)和紫杉醇(PTX)抗癌药物分子的双重递送。使用了几种数量来研究 DOX 和 PTX 在载体上的吸附机制。结果表明,药物分子自发地向载体移动并形成稳定的复合物。在药物与 BN 的相互作用中,范德华(vdW)的贡献高于静电能,这可以与药物与载体之间形成强 π-π 相互作用有关。此外,同样地,在药物吸附在 PH 表面上时,vdW 相互作用的作用大于静电能。此外,还研究了 BN 和 PH 纳米片的氧化性质。结果表明,在存在羟基的情况下,PTX 和 DOX 分子的扩散系数值增加,这可以归因于官能团的阻塞效应。由 Ramaswamy H. Sarma 交流。

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