Synthesis of Submicron CaCO3 Particles in 3D-Printed Microfluidic Chips Supporting Advection and Diffusion Mixing
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Published:2024-05-15
Issue:5
Volume:15
Page:652
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ISSN:2072-666X
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Container-title:Micromachines
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language:en
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Short-container-title:Micromachines
Author:
Reznik Ivan12ORCID, Kolesova Ekaterina13ORCID, Pestereva Anna4, Baranov Konstantin4ORCID, Osin Yury5, Bogdanov Kirill1, Swart Jacobus2, Moshkalev Stanislav6, Orlova Anna4ORCID
Affiliation:
1. International Research and Education Center for Physics of Nanostructures, ITMO University, Saint Petersburg 197101, Russia 2. Faculty of Electrical Engineering and Computing, University of Campinas, Campinas 13083-970, Brazil 3. Research Center for Translation Medicine, Sirius University, Sochi 354349, Russia 4. International Laboratory Hybrid Nanostructures for Biomedicine, ITMO University, Saint Petersburg 199034, Russia 5. Laboratory for Scientific Restoration of Precious Metals, The State Hermitage Museum, Saint Petersburg 191186, Russia 6. Center for Semiconductor Components and Nanotechnology, University of Campinas, Campinas 13083-870, Brazil
Abstract
Microfluidic technology provides a solution to the challenge of continuous CaCO3 particle synthesis. In this study, we utilized a 3D-printed microfluidic chip to synthesize CaCO3 micro- and nanoparticles in vaterite form. Our primary focus was on investigating a continuous one-phase synthesis method tailored for the crystallization of these particles. By employing a combination of confocal and scanning electron microscopy, along with Raman spectroscopy, we were able to thoroughly evaluate the synthesis efficiency. This evaluation included aspects such as particle size distribution, morphology, and polymorph composition. The results unveiled the existence of two distinct synthesis regimes within the 3D-printed microfluidic chips, which featured a channel cross-section of 2 mm2. In the first regime, which was characterized by chaotic advection, particles with an average diameter of around 2 μm were produced, thereby displaying a broad size distribution. Conversely, the second regime, marked by diffusion mixing, led to the synthesis of submicron particles (approximately 800–900 nm in diameter) and even nanosized particles (70–80 nm). This research significantly contributes valuable insights to both the understanding and optimization of microfluidic synthesis processes, particularly in achieving the controlled production of submicron and nanoscale particles.
Funder
The Ministry of Education and Science of the Russian Federation CNPq
Reference45 articles.
1. Hafeez, M., Celia, C., and Petrikaite, V. (2021). Challenges towards targeted drug delivery in cancer nanomedicines. Processes, 9. 2. Yao, Y., Zhou, Y., Liu, L., Xu, Y., Chen, Q., Wang, Y., Wu, S., Deng, Y., Zhang, J., and Shao, A. (2020). Nanoparticle-based drug delivery in cancer therapy and its role in overcoming drug resistance. Front. Mol. Biosci., 7. 3. Kuznetsova, V., Osipova, V., Tkach, A., Miropoltsev, M., Kurshanov, D., Sokolova, A., Cherevkov, S., Zakharov, V., Fedorov, A., and Baranov, A. (2021). Lab-on-Microsphere—FRET-Based Multiplex Sensor Platform. Nanomaterials, 11. 4. Sun, R., Xiang, J., Zhou, Q., Piao, Y., Tang, J., Shao, S., Zhou, Z., Bae, Y., and Shen, Y. (2022). The tumor EPR effect for cancer drug delivery: Current status, limitations, and alternatives. Adv. Drug Deliv. Rev., 191. 5. Zi, Y., Yang, K., He, J., Wu, Z., Liu, J., and Zhang, W. (2022). Strategies to enhance drug delivery to solid tumors by harnessing the EPR effects and alternative targeting mechanisms. Adv. Drug Deliv. Rev., 188.
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