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- Conflict of Interest
- In relation to this article, we declare that there is no conflict of interest.
- Publication history
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Received October 18, 2024
Revised May 6, 2025
Accepted May 8, 2025
Available online July 25, 2025
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This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits
unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Most Cited
Effi cient Synthesis of Magnetic-Silica Particles for Nucleic Acid Extraction in Diagnostics Based on Washing-Free Magnetic Fine Nanoparticles
https://doi.org/10.1007/s11814-025-00480-7
Abstract
Magnetic-silica particles (MAGSi) have been widely used for rapid and large-scale nucleic acid extraction. However, the
synthesis procedure normally involves washing steps, which will produce chemical waste and are time-consuming. In this
study, we synthesized magnetic-silica fi ne particles by eliminating the washing step in magnetic nanoparticle production,
thereby improving environmental sustainability and reducing synthesis time. First, magnetic nanoparticles (MNP) with sizes
averaging around 100 nm (based on dynamic light scattering (DLS) data) were synthesized via co-precipitation continued
with silica coating by the Stöber method, without washing the Fe 3 O 4 nanoparticles. Compared to the washed MNP, the
unwashed MNP exhibited similar magnetization, with 47.85 emu/g for the unwashed and 47.10 emu/g for the washed MNP.
The unwashed MNP was also successfully coated with silica, which resulted in a decrease in magnetization (5.00 emu/g)
with a Fe 3 O 4 :SiO 2 mass ratio of 1:8. Compared to MAGSi synthesized by washed MNP, the unwashed MNP produced
MAGSi with a larger size (~ 1700 nm compared to 320 nm based on the DLS data), more pronounced SiO 2 FTIR peaks, and
lower magnetization due to a thicker SiO 2 layer. The MAGSi synthesized using the unwashed MNP is still eff ectively able
to extract RNA and DNA from viral (SARS-CoV-2 and Canine Distemper Virus) and bacterial (Leptospira spp.) samples, as
validated through PCR and qRT-PCR. This work introduces a practical and sustainable approach for synthesizing MAGSi,
demonstrating their utility in nucleic acid extraction without compromising performance.

