Hu Junyi, Cao Jingjing, Lin Jinwei, Xu Leilei
State Key Laboratory of Advanced Technology for Materials Synthesis and Processing, International School of Materials Science and Engineering, Wuhan University of Technology, Wuhan 430070, China.
Nanomaterials (Basel). 2024 Mar 14;14(6):519. doi: 10.3390/nano14060519.
Serotonin-based nanomaterials have been positioned as promising contenders for constructing multifunctional biomedical nanoplatforms due to notable biocompatibility, advantageous charge properties, and chemical adaptability. The elaborately designed structure and morphology are significant for their applications as functional carriers. In this study, we fabricated anisotropic bowl-like mesoporous polyserotonin (PST) nanoparticles with a diameter of approximately 170 nm through nano-emulsion polymerization, employing P123/F127 as a dual-soft template and 1,3,5-trimethylbenzene (TMB) as both pore expander and emulsion template. Their formation can be attributed to the synchronized assembly of P123/F127/TMB, along with the concurrent manifestation of anisotropic nucleation and growth on the TMB emulsion droplet surface. Meanwhile, the morphology of PST nanoparticles can be regulated from sphere- to bowl-like, with a particle size distribution ranging from 432 nm to 100 nm, experiencing a transformation from a dendritic, cylindrical open mesoporous structure to an approximately non-porous structure by altering the reaction parameters. The well-defined mesopores, intrinsic asymmetry, and pH-dependent charge reversal characteristics enable the as-prepared mesoporous bowl-like PST nanoparticles' potential for constructing responsive biomedical nanomotors through incorporating some catalytic functional materials, 3.5 nm CeO nanoenzymes, as a demonstration. The constructed nanomotors demonstrate remarkable autonomous movement capabilities under physiological HO concentrations, even at an extremely low concentration of 0.05 mM, showcasing the 51.58 body length/s velocity. Furthermore, they can also respond to physiological pH values ranging from 4.4 to 7.4, exhibiting reduced mobility with increasing pH. This charge reversal-based responsive nanomotor design utilizing PST nanoparticles holds great promise for advancing the application of nanomotors within complex biological systems.
基于血清素的纳米材料因其显著的生物相容性、有利的电荷性质和化学适应性,已被定位为构建多功能生物医学纳米平台的有前途的竞争者。精心设计的结构和形态对其作为功能载体的应用具有重要意义。在本研究中,我们通过纳米乳液聚合制备了直径约为170 nm的各向异性碗状介孔聚血清素(PST)纳米颗粒,采用P123/F127作为双软模板,1,3,5-三甲基苯(TMB)作为孔扩张剂和乳液模板。它们的形成可归因于P123/F127/TMB的同步组装,以及在TMB乳液滴表面同时出现的各向异性成核和生长。同时,PST纳米颗粒的形态可以从球形调节为碗状,粒径分布范围为432 nm至100 nm,通过改变反应参数,经历从树枝状、圆柱形开放介孔结构到近似无孔结构的转变。明确的介孔、固有的不对称性和pH依赖的电荷反转特性使得所制备的介孔碗状PST纳米颗粒有潜力通过掺入一些催化功能材料(作为示范的3.5 nm CeO纳米酶)来构建响应性生物医学纳米马达。所构建的纳米马达在生理HO浓度下表现出显著的自主运动能力,即使在极低浓度0.05 mM下,也展示出51.58体长/秒的速度。此外,它们还可以响应4.4至7.4的生理pH值,随着pH值的增加,迁移率降低。这种利用PST纳米颗粒的基于电荷反转的响应性纳米马达设计在推进纳米马达在复杂生物系统中的应用方面具有很大的前景。