Department of Polymer Science and Engineering, State Key Laboratory of Coordination Chemistry and Collaborative Innovation Center of Chemistry for Life Sciences, Key Laboratory of High Performance Polymer Material and Technology of Ministry of Education, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China.
Soft Matter. 2020 Mar 28;16(12):3088-3095. doi: 10.1039/d0sm00069h. Epub 2020 Mar 9.
We investigated the co-assembly of amphiphilic diblock copolymers in solutions containing drugs and functional nanoparticles using the dissipative particle dynamics (DPD) method. By controlling the size and the concentration of the functional nanoparticles, the length of the hydrophobic blocks, and the interaction parameters between the hydrophobic block/solvent and the functional nanoparticles, we obtained the desired aggregates to load drugs. The aggregates loaded with drugs can be disk-like micelles, sphere-like micelles and vesicles with functional nanoparticles on the surface. When the solvent environment changes, the drugs loaded in the functional vesicles can release into the solvent. The release content is critically dependent on the repulsive interaction between the drugs and the solvent. The dynamic curve of drug release is obtained. The result is in agreement with the experiments about drug release. Our studies showed that we can precisely control the formation of functional vesicles to load and release drugs. Loading drugs in the process of self-assembly and controlling the release have broad potential in the field of clinical medicine and adding functional nanoparticles can be of great help in drug delivery and medical diagnosis.
我们使用耗散粒子动力学(DPD)方法研究了含有药物和功能纳米粒子的溶液中两亲性嵌段共聚物的共组装。通过控制功能纳米粒子的尺寸和浓度、疏水嵌段的长度以及疏水嵌段/溶剂与功能纳米粒子之间的相互作用参数,我们获得了负载药物所需的期望聚集体。负载药物的聚集体可以是具有功能纳米粒子的盘状胶束、球状胶束和囊泡。当溶剂环境发生变化时,负载在功能囊泡中的药物可以释放到溶剂中。药物释放的含量取决于药物和溶剂之间的排斥相互作用。得到了药物释放的动力学曲线。结果与药物释放的实验结果一致。我们的研究表明,我们可以精确控制功能囊泡的形成来负载和释放药物。在自组装过程中负载药物并控制释放,在临床医学领域具有广阔的应用前景,添加功能纳米粒子在药物输送和医学诊断方面有很大的帮助。