论文标题
硅纳米酮对靶向药物输送的细胞膜自密封能力的影响 - 计算机仿真研究
Influence of silicon nanocone on cell membrane self-sealing capabilities for targeted drug delivery -- computer simulation study
论文作者
论文摘要
货物传递到生物细胞的有效和非侵入性技术是生物医学研究的重点,因为它们对靶向药物疗法具有巨大的潜在重要性。因此,正在努力研究使用基于纳米的生物相容性材料作为可以促进这项任务的系统的特征,同时确保对细胞膜进行适当的自密封。在这里,我们研究了通过应用转导的分子动力学(SMD)技术来研究纳米膀胱的凹痕和戒断对磷脂膜的影响。我们的结果表明,撤回过程直接取决于纳米酮的初始位置。如果从更大的深度开始撤离时,平均力和工作更为重要。该结果归因于膜分子的纳米酮和脂质尾巴之间的疏水相互作用。此外,当缩进器从较低的初始深度启动时,从膜中除去的脂质数量比更深的凹痕小几倍。纳米结构辅助药物输送的最少侵入性方法对于医学中的可能应用至关重要。因此,这项工作中提出的结果可能有助于与纳米材料的有效且安全的药物输送。
Efficient and non-invasive techniques of cargo delivery to biological cells are the focus of biomedical research because of their great potential importance for targeted drug therapy. Therefore, much effort is being made to study the characteristics of using nano-based biocompatible materials as systems that can facilitate this task while ensuring appropriate self-sealing of the cell membrane. Here, we study the effects of indentation and withdrawal of nanospear on phospholipid membrane by applying steered molecular dynamics (SMD) technique. Our results show that the withdrawal process directly depends on the initial position of the nanocone. The average force and work are considerably more significant in case of the withdrawal starting from a larger depth. This result is attributed to stronger hydrophobic interactions between the nanocone and lipid tails of the membrane molecules. Furthermore, when the indenter was started from the lower initial depth, the number of lipids removed from the membrane was several times smaller than the deeper indentation. The choice of the least invasive method for nanostructure-assisted drug delivery is crucial for possible applications in medicine. Therefore, the results presented in this work might be helpful in efficient and safe drug delivery with nanomaterials.