Korenkov Egor S, Cherkasov Vladimir R, Nikitin Maxim P
Moscow Center for Advanced Studies, 123592 Moscow, Russia.
Moscow Institute of Physics and Technology (State University), 117303 Moscow, Russia.
HardwareX. 2024 Jul 1;19:e00554. doi: 10.1016/j.ohx.2024.e00554. eCollection 2024 Sep.
Synthesis of nanoparticles is typically carried out in batch procedures, which offer limited control of parameters, and a narrow range of possible batch volumes. In contrast, flow synthesis systems, usually having a microfluidic chip as a crucial part, are devoid of these drawbacks. However, large scale devices - millifluidic systems - may offer several advantages over microfluidic systems, such as easier and cheaper production, enhanced throughput, and reduced channel clogging. Here we report a millifluidic system for the generation of protein nanoparticles, using the flow format of the original swift thermal formation technology (STF), which can process batch volume ranging from 100 µl to any practically significant amount. Capabilities of the system are demonstrated with model synthesis of Epirubicin-encapsulated BSA nanoparticles. A better degree of scalability of the synthesis over batch procedure is shown: with a 10-fold working volume increase, hydrodynamic diameter and loading capacity changed by only 10 % and 1 % respectively, compared to 60 % and 30 % for the batch synthesis. Additionally, we provide all engineering drawings, electrical circuits, programming code and nuances of assembly and operation, so that our findings can be easily reproduced. The ease of construction of the device and the superior characteristics of the resulting nanoparticles compared to the batch method indicate application potential in both the biomedical research and industrial spheres.
纳米颗粒的合成通常采用分批法进行,这种方法对参数的控制有限,且可能的批量范围较窄。相比之下,流动合成系统通常以微流控芯片为关键部件,不存在这些缺点。然而,大规模设备——毫流控系统——可能比微流控系统具有一些优势,比如生产更简便、成本更低、通量更高以及通道堵塞减少。在此,我们报告一种用于生成蛋白质纳米颗粒的毫流控系统,它采用原始快速热形成技术(STF)的流动形式,可处理从100微升至任何实际显著量的批量。通过合成表柔比星包封的牛血清白蛋白纳米颗粒的模型实验展示了该系统的能力。与分批法相比,合成的可扩展性更高:工作体积增加10倍时,与分批合成中分别变化60%和30%相比,流体动力学直径和负载能力仅分别变化10%和1%。此外,我们提供了所有工程图纸、电路、编程代码以及组装和操作的细节,以便我们的研究结果能够轻松重现。该设备易于构建,且与分批法相比,所得纳米颗粒具有优异特性,这表明其在生物医学研究和工业领域均具有应用潜力。