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Protein corona composition of superparamagnetic iron oxide nanoparticles with various physico-chemical properties and coatings.

作者信息

Sakulkhu Usawadee, Mahmoudi Morteza, Maurizi Lionel, Salaklang Jatuporn, Hofmann Heinrich

机构信息

Laboratory of Powder Technology, École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.

1] Department of Nanotechnology, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran [2] Nanotechnology Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Sci Rep. 2014 May 21;4:5020. doi: 10.1038/srep05020.


DOI:10.1038/srep05020
PMID:24846348
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5381372/
Abstract

Because of their biocompatibility and unique magnetic properties, superparamagnetic iron oxide nanoparticles NPs (SPIONs) are recognized as some of the most prominent agents for theranostic applications. Thus, understanding the interaction of SPIONs with biological systems is important for their safe design and efficient applications. In this study, SPIONs were coated with 2 different polymers: polyvinyl alcohol polymer (PVA) and dextran. The obtained NPs with different surface charges (positive, neutral, and negative) were used as a model study of the effect of surface charges and surface polymer materials on protein adsorption using a magnetic separator. We found that the PVA-coated SPIONs with negative and neutral surface charge adsorbed more serum proteins than the dextran-coated SPIONs, which resulted in higher blood circulation time for PVA-coated NPs than the dextran-coated ones. Highly abundant proteins such as serum albumin, serotransferrin, prothrombin, alpha-fetoprotein, and kininogen-1 were commonly found on both PVA- and dextran-coated SPIONs. By increasing the ionic strength, soft- and hard-corona proteins were observed on 3 types of PVA-SPIONs. However, the tightly bound proteins were observed only on negatively charged PVA-coated SPIONs after the strong protein elution.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba7a/5381372/2a1ca16f1a97/srep05020-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba7a/5381372/e7b0fcdc3b3e/srep05020-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba7a/5381372/01961961312d/srep05020-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba7a/5381372/d0f0f94e994a/srep05020-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba7a/5381372/d8e892e7fcde/srep05020-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba7a/5381372/0b90eab9f69f/srep05020-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba7a/5381372/f89c3107d7b8/srep05020-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba7a/5381372/4a5e99b1757e/srep05020-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba7a/5381372/2a1ca16f1a97/srep05020-f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba7a/5381372/e7b0fcdc3b3e/srep05020-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba7a/5381372/01961961312d/srep05020-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba7a/5381372/d0f0f94e994a/srep05020-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba7a/5381372/d8e892e7fcde/srep05020-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba7a/5381372/0b90eab9f69f/srep05020-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba7a/5381372/f89c3107d7b8/srep05020-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba7a/5381372/4a5e99b1757e/srep05020-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba7a/5381372/2a1ca16f1a97/srep05020-f8.jpg

相似文献

[1]
Protein corona composition of superparamagnetic iron oxide nanoparticles with various physico-chemical properties and coatings.

Sci Rep. 2014-5-21

[2]
Significance of surface charge and shell material of superparamagnetic iron oxide nanoparticle (SPION) based core/shell nanoparticles on the composition of the protein corona.

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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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Nanoscale. 2016-5-31

[10]
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ACS Appl Mater Interfaces. 2014-9-10

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[3]
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[4]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
A fast and reproducible method to quantify magnetic nanoparticle biodistribution.

Analyst. 2014-1-21

[2]
Slight temperature changes affect protein affinity and cellular uptake/toxicity of nanoparticles.

Nanoscale. 2013-3-19

[3]
Emerging techniques in proteomics for probing nano-bio interactions.

ACS Nano. 2012-12-7

[4]
Cell type-specific activation of AKT and ERK signaling pathways by small negatively-charged magnetic nanoparticles.

Sci Rep. 2012-11-16

[5]
Significance of cell "observer" and protein source in nanobiosciences.

J Colloid Interface Sci. 2012-10-22

[6]
Effects of the presence or absence of a protein corona on silica nanoparticle uptake and impact on cells.

ACS Nano. 2012-6-29

[7]
Limitations and caveats of magnetic cell labeling using transfection agent complexed iron oxide nanoparticles.

Contrast Media Mol Imaging. 2012

[8]
Silver-coated engineered magnetic nanoparticles are promising for the success in the fight against antibacterial resistance threat.

ACS Nano. 2012-3-7

[9]
Do plasma proteins distinguish between liposomes of varying charge density?

J Proteomics. 2012-1-14

[10]
Assessing the in vitro and in vivo toxicity of superparamagnetic iron oxide nanoparticles.

Chem Rev. 2012-4-11

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