Bovone Giovanni, Cousin Lucien, Steiner Fabian, Tibbitt Mark W
Macromolecular Engineering Laboratory, Department of Mechanical and Process Engineering, ETH Zurich, 8092 Zurich, Switzerland.
Macromolecules. 2022 Sep 27;55(18):8040-8048. doi: 10.1021/acs.macromol.2c00907. Epub 2022 Sep 9.
Control of the properties of nanoparticles (NPs), including size, is critical for their application in biomedicine and engineering. Polymeric NPs are commonly produced by nanoprecipitation, where a solvent containing a block copolymer is mixed rapidly with a nonsolvent, such as water. Empirical evidence suggests that the choice of solvent influences NP size; yet, the specific mechanism remains unclear. Here, we show that solvent controls NP size by limiting block copolymer assembly. In the initial stages of mixing, polymers assemble into dynamic aggregates that grow via polymer exchange. At later stages of mixing, further growth is prevented beyond a solvent-specific water fraction. Thus, the solvent sets NP size by controlling the extent of dynamic growth up to growth arrest. An model based on spinodal decomposition corroborates our proposed mechanism, explaining how size scales with the solvent-dependent critical water fraction of growth arrest and enabling more efficient NP engineering.
控制纳米颗粒(NPs)的性质,包括尺寸,对于它们在生物医学和工程领域的应用至关重要。聚合物纳米颗粒通常通过纳米沉淀法制备,即将含有嵌段共聚物的溶剂与非溶剂(如水)快速混合。实验证据表明,溶剂的选择会影响纳米颗粒的尺寸;然而,具体机制仍不清楚。在这里,我们表明溶剂通过限制嵌段共聚物的组装来控制纳米颗粒的尺寸。在混合的初始阶段,聚合物组装成动态聚集体,通过聚合物交换而生长。在混合的后期阶段,超过特定溶剂的水含量后,进一步的生长就会受到抑制。因此,溶剂通过控制动态生长直至生长停止的程度来设定纳米颗粒的尺寸。基于旋节线分解的模型证实了我们提出的机制,解释了尺寸如何随着生长停止的溶剂依赖性临界水含量而变化,并实现了更高效的纳米颗粒工程。