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Synthesis of Biocompatible Superparamagnetic Iron Oxide Nanoparticles (SPION) under Different Microfluidic Regimes
[Image: see text] Superparamagnetic iron oxide nanoparticles (SPION) have a great potential in both diagnostic and therapeutic applications as they provide contrast in magnetic resonance imaging techniques and allow magnetic hyperthermia and drug delivery. Though various types of SPION are commercia...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9615998/ https://www.ncbi.nlm.nih.gov/pubmed/36223272 http://dx.doi.org/10.1021/acsami.2c13156 |
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author | Schemberg, Jörg Abbassi, Abdelouahad El Lindenbauer, Annerose Chen, Li-Yu Grodrian, Andreas Nakos, Xenia Apte, Gurunath Khan, Nida Kraupner, Alexander Nguyen, Thi-Huong Gastrock, Gunter |
author_facet | Schemberg, Jörg Abbassi, Abdelouahad El Lindenbauer, Annerose Chen, Li-Yu Grodrian, Andreas Nakos, Xenia Apte, Gurunath Khan, Nida Kraupner, Alexander Nguyen, Thi-Huong Gastrock, Gunter |
author_sort | Schemberg, Jörg |
collection | PubMed |
description | [Image: see text] Superparamagnetic iron oxide nanoparticles (SPION) have a great potential in both diagnostic and therapeutic applications as they provide contrast in magnetic resonance imaging techniques and allow magnetic hyperthermia and drug delivery. Though various types of SPION are commercially available, efforts to improve the quality of SPION are highly in demand. Here, we describe a strategy for optimization of SPION synthesis under microfluidics using the coprecipitation approach. Synthesis parameters such as temperature, pH, iron salt concentration, and coating materials were investigated in continuous and segmented flows. Continuous flow allowed synthesizing particles of a smaller size and higher stability than segmented flow, while both conditions improved the quality of particles compared to batch synthesis. The most stable particles were obtained at a synthesis condition of 6.5 M NH(4)OH base, iron salt (Fe(2+)/Fe(3+)) concentration ratio of 4.3/8.6, carboxymethyl dextran coating of 20 mg/mL, and temperature of 70 °C. The synthesized SPION exhibited a good efficiency in labeling of human platelets and did not impair cells. Our study under flow conditions provides an optimal protocol for the synthesis of better and biocompatible SPION that contributes to the development of nanoparticles for medical applications. |
format | Online Article Text |
id | pubmed-9615998 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-96159982023-10-12 Synthesis of Biocompatible Superparamagnetic Iron Oxide Nanoparticles (SPION) under Different Microfluidic Regimes Schemberg, Jörg Abbassi, Abdelouahad El Lindenbauer, Annerose Chen, Li-Yu Grodrian, Andreas Nakos, Xenia Apte, Gurunath Khan, Nida Kraupner, Alexander Nguyen, Thi-Huong Gastrock, Gunter ACS Appl Mater Interfaces [Image: see text] Superparamagnetic iron oxide nanoparticles (SPION) have a great potential in both diagnostic and therapeutic applications as they provide contrast in magnetic resonance imaging techniques and allow magnetic hyperthermia and drug delivery. Though various types of SPION are commercially available, efforts to improve the quality of SPION are highly in demand. Here, we describe a strategy for optimization of SPION synthesis under microfluidics using the coprecipitation approach. Synthesis parameters such as temperature, pH, iron salt concentration, and coating materials were investigated in continuous and segmented flows. Continuous flow allowed synthesizing particles of a smaller size and higher stability than segmented flow, while both conditions improved the quality of particles compared to batch synthesis. The most stable particles were obtained at a synthesis condition of 6.5 M NH(4)OH base, iron salt (Fe(2+)/Fe(3+)) concentration ratio of 4.3/8.6, carboxymethyl dextran coating of 20 mg/mL, and temperature of 70 °C. The synthesized SPION exhibited a good efficiency in labeling of human platelets and did not impair cells. Our study under flow conditions provides an optimal protocol for the synthesis of better and biocompatible SPION that contributes to the development of nanoparticles for medical applications. American Chemical Society 2022-10-12 2022-10-26 /pmc/articles/PMC9615998/ /pubmed/36223272 http://dx.doi.org/10.1021/acsami.2c13156 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Schemberg, Jörg Abbassi, Abdelouahad El Lindenbauer, Annerose Chen, Li-Yu Grodrian, Andreas Nakos, Xenia Apte, Gurunath Khan, Nida Kraupner, Alexander Nguyen, Thi-Huong Gastrock, Gunter Synthesis of Biocompatible Superparamagnetic Iron Oxide Nanoparticles (SPION) under Different Microfluidic Regimes |
title | Synthesis of Biocompatible
Superparamagnetic Iron
Oxide Nanoparticles (SPION) under Different Microfluidic Regimes |
title_full | Synthesis of Biocompatible
Superparamagnetic Iron
Oxide Nanoparticles (SPION) under Different Microfluidic Regimes |
title_fullStr | Synthesis of Biocompatible
Superparamagnetic Iron
Oxide Nanoparticles (SPION) under Different Microfluidic Regimes |
title_full_unstemmed | Synthesis of Biocompatible
Superparamagnetic Iron
Oxide Nanoparticles (SPION) under Different Microfluidic Regimes |
title_short | Synthesis of Biocompatible
Superparamagnetic Iron
Oxide Nanoparticles (SPION) under Different Microfluidic Regimes |
title_sort | synthesis of biocompatible
superparamagnetic iron
oxide nanoparticles (spion) under different microfluidic regimes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9615998/ https://www.ncbi.nlm.nih.gov/pubmed/36223272 http://dx.doi.org/10.1021/acsami.2c13156 |
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