School of Physics and Engineering, ITMO University, 191002 St. Petersburg, Russian Federation.
RM Gorbacheva Research Institute of Pediatric Oncology, Hematology and Transplantation, Pavlov University, 197022 St. Petersburg, Russian Federation.
Biomater Adv. 2024 Jul;161:213904. doi: 10.1016/j.bioadv.2024.213904. Epub 2024 May 23.
Engineered calcium carbonate (CaCO) particles are extensively used as drug delivery systems due to their availability, biological compatibility, biodegradability, and cost-effective production. The synthesis procedure of CaCO particles, however, suffers from poor reproducibility. Furthermore, reducing the size of CaCO particles to <100 nm requires the use of additives in the reaction, which increases the total reaction time. Here we propose on-chip synthesis and loading of nanoscaled CaCO particles using microfluidics. After the development and fabrication of a microfluidic device, we optimized the synthesis of CaCO NPs by varying different parameters such as flow rates in the microfluidic channels, concentration of reagents, and the reaction time. To prove the versatility of the used synthesis route, we performed single and double loading of CaCO NPs with various compounds (Doxorubicin, Cy5 or FITC conjugated with BSA, and DNA) using the same microfluidic device. Further, the on-chip loaded CaCO NPs were used as carriers to transfer compounds to model cells. We have developed a microfluidic synthesis method that opens up a new pathway for easy on-chip fabrication of functional nanoparticles for clinical use.
由于其可用性、生物相容性、可生物降解性和具有成本效益的生产,工程碳酸钙 (CaCO) 颗粒被广泛用作药物输送系统。然而,CaCO 颗粒的合成工艺重复性差。此外,将 CaCO 颗粒的尺寸减小到 <100nm 需要在反应中使用添加剂,这会增加总反应时间。在这里,我们提出使用微流控技术进行纳米级 CaCO 颗粒的片上合成和加载。在开发和制造微流控设备之后,我们通过改变微流道中的流速、试剂浓度和反应时间等不同参数来优化 CaCO NPs 的合成。为了证明所使用的合成路线的多功能性,我们使用相同的微流控设备对 CaCO NPs 进行了单次和双加载,加载的化合物有(阿霉素、Cy5 或 FITC 与 BSA 偶联物,以及 DNA)。此外,片上加载的 CaCO NPs 被用作载体将化合物传递到模型细胞中。我们已经开发出一种微流控合成方法,为临床应用的功能性纳米粒子的易于片上制造开辟了新途径。