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The influence of surface functionalization on the enhanced internalization of magnetic nanoparticles in cancer cells
Abstract
The internalization and biocompatibility of iron oxide nanoparticles surface functionalized with four differently charged carbohydrates have been tested in the human cervical carcinoma cell line (HeLa). Neutral, positive, and negative iron oxide nanoparticles were obtained by coating with dextran, aminodextran, heparin, and dimercaptosuccinic acid, resulting in colloidal suspensions stable at pH 7 with similar aggregate size. No intracellular uptake was detected in cells incubated with neutral charged nanoparticles, while negative particles showed different behaviour depending on the nature of the coating. Thus, dimercaptosuccinic-coated nanoparticles showed low cellular uptake with non-toxic effects, while heparin-coated particles showed cellular uptake only at high nanoparticle concentrations and induced abnormal mitotic spindle configurations. Finally, cationic magnetic nanoparticles show excellent properties for possible in vivo biomedical applications such as cell tracking by magnetic resonance imaging (MRI) and cancer treatment by hyperthermia: (i) they enter into cells with high effectiveness, and are localized in endosomes; (ii) they can be easily detected inside cells by optical microscopy, (iii) they are retained for relatively long periods of time, and (iv) they do not induce any cytotoxicity.
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“Anionic nanoparticles are less efficiently internalized than cationic and neutral particles [40,41,42,43].”
From Targeted Nano-Drug Delivery of Colchicine against Colon Cancer Cells by Means of Mesoporous Silica Nanoparticles (2020) · cites this paper as [40]
In the citing paper
“The surface charge of particles (neutral, anionic, and cationic charges) determines their internalization into cells.”
From Targeted Nano-Drug Delivery of Colchicine against Colon Cancer Cells by Means of Mesoporous Silica Nanoparticles (2020) · cites this paper as [40]
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AbouAitah, K., Hassan, H. A., Swiderska-Sroda, A., Gohar, L., Shaker, O. G., Wojnarowicz, J., Opalinska, A., Smalc-Koziorowska, J., Gierlotka, S., & Lojkowski, W. (2020) · Cancers · doi:10.3390/cancers12010144 · Cited by 105
Magnetic Iron Nanoparticles: Synthesis, Surface Enhancements, and Biological Challenges
Vargas-Ortiz, J. R., Gonzalez, C., & Esquivel, K. (2022) · Processes · doi:10.3390/pr10112282 · Cited by 62
NDong, C., Tate, J. A., Kett, W. C., Batra, J., Demidenko, E., Lewis, L. D., Hoopes, P. J., Gerngross, T. U., & Griswold, K. E. (2015) · PLOS ONE · doi:10.1371/journal.pone.0115636 · Cited by 50
Recent Advances in the Development of Magnetic Nanoparticles for Biomedical Applications
Monteserín, M., Larumbe, S., Martínez, A. V., Burgui, S., & Francisco Martín, L. (2021) · Journal of Nanoscience and Nanotechnology · doi:10.1166/jnn.2021.19062 · Cited by 27
Metadata
- Authors
- Villanueva, A., Cañete, M., Roca, A. G., Calero, M., Veintemillas-Verdaguer, S., Serna, C. J., del Puerto Morales, M., & Miranda, R.
- Venue
- Nanotechnology
- Publisher
- IOP Publishing
- Published
- 2009-02-24
- Volume
- 20
- Issue
- 11
- Pages
- 115103
- ISSN
- 0957-4484
- 1361-6528
- Cited by
- 299
- References
- 0
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