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Antioxidant capacities of the selenium nanoparticles stabilized by chitosan.

作者信息

Zhai Xiaona, Zhang Chunyue, Zhao Guanghua, Stoll Serge, Ren Fazheng, Leng Xiaojing

机构信息

Beijing Advanced Innovation Center for Food Nutrition and Human Health, Beijing Laboratory for Food Quality and Safety, Beijing Dairy Industry Innovation Team, College of Food Science & Nutritional Engineering, China Agricultural University, Beijing, 100083, China.

Group of Environmental Physical Chemistry, F.-A. Forel Institute, University of Geneva, Geneva, Switzerland.

出版信息

J Nanobiotechnology. 2017 Jan 5;15(1):4. doi: 10.1186/s12951-016-0243-4.


DOI:10.1186/s12951-016-0243-4
PMID:28056992
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5217424/
Abstract

BACKGROUNDS: Selenium (Se) as one of the essential trace elements for human plays an important role in the oxidation reduction system. But the high toxicity of Se limits its application. In this case, the element Se with zero oxidation state (Se) has captured our attention because of its low toxicity and excellent bioavailability. However, Se is very unstable and easily changes into the inactive form. By now many efforts have been done to protect its stability. And this work was conducted to explore the antioxidant capacities of the stable Se nanoparticles (SeNPs) stabilized using chitosan (CS) with different molecular weights (Mws) (CS-SeNPs). RESULTS: The different Mws CS-SeNPs could form uniform sphere particles with a size of about 103 nm after 30 days. The antioxidant tests of the DPPH, ABTS, and lipid peroxide models showed that these CS-SeNPs could scavenge free radicals at different levels. And the 1 month old SeNPs held the higher ABTS scavenging ability that the value could reach up to 87.45 ± 7.63% and 89.44 ± 5.03% of CS(l)-SeNPs and CS(h)-SeNPs, respectively. In the cell test using BABLC-3T3 or Caco-2, the production of the intracellular reactive oxygen species (ROS) could be inhibited in a Se concentration-dependent manner. The topical or oral administration of CS-SeNPs, particularly the Se nanoparticles stabilized with low molecular weight CS, CS(l)-SeNPs, and treated with a 30-day storage process, could efficiently protect glutathione peroxidase (GPx) activity and prevent the lipofusin formation induced by UV-radiation or D-galactose in mice, respectively. Such effects were more evident in viscera than in skin. The acute toxicity of CS(l)-SeNPs was tenfold lower than that of HSeO. CONCLUSIONS: Our work could demonstrate the CS-SeNPs hold a lower toxicity and a 30-day storage process could enhance the antioxidant capacities. All CS-SeNPs could penetrate the tissues and perform their antioxidant effects, especially the CS(l)-SeNPs in mice models. What's more, the antioxidant capacities of CS-SeNPs were more evident in viscera than in skin.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439b/5217424/f7d528da0514/12951_2016_243_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439b/5217424/266a3a53325b/12951_2016_243_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439b/5217424/93dd326360fc/12951_2016_243_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439b/5217424/34e22c617230/12951_2016_243_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439b/5217424/51bf8091e70a/12951_2016_243_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439b/5217424/074336a09077/12951_2016_243_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439b/5217424/094075926d64/12951_2016_243_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439b/5217424/f7d528da0514/12951_2016_243_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439b/5217424/266a3a53325b/12951_2016_243_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439b/5217424/93dd326360fc/12951_2016_243_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439b/5217424/34e22c617230/12951_2016_243_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439b/5217424/51bf8091e70a/12951_2016_243_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439b/5217424/074336a09077/12951_2016_243_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439b/5217424/094075926d64/12951_2016_243_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439b/5217424/f7d528da0514/12951_2016_243_Fig7_HTML.jpg

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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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本文引用的文献

[1]
Synthesis, characterization, and controlled release of selenium nanoparticles stabilized by chitosan of different molecular weights.

Carbohydr Polym. 2015-7-29

[2]
Effects of selenium-chitosan on blood selenium concentration, antioxidation status, and cellular and humoral immunity in mice.

Biol Trace Elem Res. 2015-6

[3]
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Colloids Surf B Biointerfaces. 2014-10-1

[4]
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Dalton Trans. 2014-1-28

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Biomaterials. 2013-9-30

[6]
Protonation of epigallocatechin-3-gallate (EGCG) results in massive aggregation and reduced oral bioavailability of EGCG-dispersed selenium nanoparticles.

J Agric Food Chem. 2013-7-17

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J Proteomics. 2013-1-18

[8]
PEG-nanolized ultrasmall selenium nanoparticles overcome drug resistance in hepatocellular carcinoma HepG2 cells through induction of mitochondria dysfunction.

Int J Nanomedicine. 2012-7-23

[9]
Selenium nanoparticles as a carrier of 5-fluorouracil to achieve anticancer synergism.

ACS Nano. 2012-7-26

[10]
Creation of highly stable selenium nanoparticles capped with hyperbranched polysaccharide in water.

Langmuir. 2010-10-21

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