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核心技术专利:CN118964589B侵权必究
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Biocompatible coated magnetosome minerals with various organization and cellular interaction properties induce cytotoxicity towards RG-2 and GL-261 glioma cells in the presence of an alternating magnetic field.

作者信息

Hamdous Yasmina, Chebbi Imène, Mandawala Chalani, Le Fèvre Raphael, Guyot François, Seksek Olivier, Alphandéry Edouard

机构信息

Nanobacterie, 36 boulevard Flandrin, 75116, Paris, France.

Laboratoire d'Imagerie et Modélisation en Neurobiologie et Cancérologie (IMNC), Campus Universitaire, Bât. 440, 15 rue Georges Clemenceau, 91406, Orsay Cedex, France.

出版信息

J Nanobiotechnology. 2017 Oct 17;15(1):74. doi: 10.1186/s12951-017-0293-2.


DOI:10.1186/s12951-017-0293-2
PMID:29041937
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5646109/
Abstract

BACKGROUND: Biologics magnetics nanoparticles, magnetosomes, attract attention because of their magnetic characteristics and potential applications. The aim of the present study was to develop and characterize novel magnetosomes, which were extracted from magnetotactic bacteria, purified to produce apyrogen magnetosome minerals, and then coated with Chitosan, Neridronate, or Polyethyleneimine. It yielded stable magnetosomes designated as M-Chi, M-Neri, and M-PEI, respectively. Nanoparticle biocompatibility was evaluated on mouse fibroblast cells (3T3), mouse glioblastoma cells (GL-261) and rat glioblastoma cells (RG-2). We also tested these nanoparticles for magnetic hyperthermia treatment of tumor in vitro on two tumor cell lines GL-261 and RG-2 under the application of an alternating magnetic field. Heating, efficacy and internalization properties were then evaluated. RESULTS: Nanoparticles coated with chitosan, polyethyleneimine and neridronate are apyrogen, biocompatible and stable in aqueous suspension. The presence of a thin coating in M-Chi and M-PEI favors an arrangement in chains of the magnetosomes, similar to that observed in magnetosomes directly extracted from magnetotactic bacteria, while the thick matrix embedding M-Neri leads to structures with an average thickness of 3.5 µm per magnetosome mineral. In the presence of GL-261 cells and upon the application of an alternating magnetic field, M-PEI and M-Chi lead to the highest specific absorption rates of 120-125 W/g. Furthermore, while M-Chi lead to rather low rates of cellular internalization, M-PEI strongly associate to cells, a property modulated by the application of an alternating magnetic field. CONCLUSIONS: Coating of purified magnetosome minerals can therefore be chosen to control the interactions of nanoparticles with cells, organization of the minerals, as well as heating and cytotoxicity properties, which are important parameters to be considered in the design of a magnetic hyperthermia treatment of tumor.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/692b/5646109/f29f146cbed7/12951_2017_293_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/692b/5646109/c3a2b5b13cf9/12951_2017_293_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/692b/5646109/4cb6131869aa/12951_2017_293_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/692b/5646109/2c208af4a480/12951_2017_293_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/692b/5646109/3562049af1a2/12951_2017_293_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/692b/5646109/bab61d8b1fa3/12951_2017_293_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/692b/5646109/f29f146cbed7/12951_2017_293_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/692b/5646109/c3a2b5b13cf9/12951_2017_293_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/692b/5646109/4cb6131869aa/12951_2017_293_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/692b/5646109/2c208af4a480/12951_2017_293_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/692b/5646109/3562049af1a2/12951_2017_293_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/692b/5646109/bab61d8b1fa3/12951_2017_293_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/692b/5646109/f29f146cbed7/12951_2017_293_Fig6_HTML.jpg

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BMC Public Health. 2024-11-8

[2]
Magnetic Hyperthermia in Glioblastoma Multiforme Treatment.

Int J Mol Sci. 2024-9-19

[3]
Evidence That a Peptide-Drug/p53 Gene Complex Promotes Cognate Gene Expression and Inhibits the Viability of Glioblastoma Cells.

Pharmaceutics. 2024-6-8

[4]
Evaluation of cell disruption technologies on magnetosome chain length and aggregation behaviour from MSR-1.

Front Bioeng Biotechnol. 2023-5-4

[5]
Neurosurgical Applications of Magnetic Hyperthermia Therapy.

Neurosurg Clin N Am. 2023-4

[6]
Progress in affinity ligand-functionalized bacterial magnetosome nanoparticles for bio-immunomagnetic separation of HBsAg protein.

PLoS One. 2022

[7]
Strategy for Avoiding Protein Corona Inhibition of Targeted Drug Delivery by Linking Recombinant Affibody Scaffold to Magnetosomes.

Int J Nanomedicine. 2022

[8]
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[9]
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[10]
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本文引用的文献

[1]
Enhanced antitumor efficacy of biocompatible magnetosomes for the magnetic hyperthermia treatment of glioblastoma.

Theranostics. 2017-10-13

[2]
Chains of magnetosomes with controlled endotoxin release and partial tumor occupation induce full destruction of intracranial U87-Luc glioma in mice under the application of an alternating magnetic field.

J Control Release. 2017-7-13

[3]
Development of non-pyrogenic magnetosome minerals coated with poly-l-lysine leading to full disappearance of intracranial U87-Luc glioblastoma in 100% of treated mice using magnetic hyperthermia.

Biomaterials. 2017-6-21

[4]
First-in-Human Study Testing a New Radioenhancer Using Nanoparticles (NBTXR3) Activated by Radiation Therapy in Patients with Locally Advanced Soft Tissue Sarcomas.

Clin Cancer Res. 2016-10-6

[5]
Magnetocontrollability of Fe7C3@C superparamagnetic nanoparticles in living cells.

J Nanobiotechnology. 2016-8-30

[6]
Magnetotactic bacteria and magnetosomes - Scope and challenges.

Mater Sci Eng C Mater Biol Appl. 2016-11-1

[7]
Cancer therapy using nanoformulated substances: scientific, regulatory and financial aspects.

Expert Rev Anticancer Ther. 2015

[8]
Polyethyleneimine-mediated synthesis of superparamagnetic iron oxide nanoparticles with enhanced sensitivity in T2 magnetic resonance imaging.

Colloids Surf B Biointerfaces. 2014-10-1

[9]
Magnetic nanoparticle-based hyperthermia for cancer treatment.

Rep Pract Oncol Radiother. 2013-11-1

[10]
Exploiting endocytosis for nanomedicines.

Cold Spring Harb Perspect Biol. 2013-11-1

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