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Physicochemical characterization and cytotoxicity assessment of sodium dodecyl sulfate (SDS) modified chitosan (SDSCS) before and after removal of aflatoxins (AFs) as a potential mycotoxin Binder.

作者信息

Jafari Afsaneh Moghaddam, Golmakani Asma, Jafari Amir Moghaddam

机构信息

Department of Chemistry, Mashhad Branch, Islamic Azad University, Mashhad, Iran.

Department of Food Chemistry, Research Institute of Food Science and Technology (RIFST), Mashhad, Iran.

出版信息

Toxicol Rep. 2024 Nov 26;13:101836. doi: 10.1016/j.toxrep.2024.101836. eCollection 2024 Dec.


DOI:10.1016/j.toxrep.2024.101836
PMID:39691817
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11650310/
Abstract

Aflatoxins in food and feed with prominent toxic effects have jeopardized public health for decades. This investigation intends to explore synthesized SDS-modified chitosan as new generation of binder for removal of aflatoxin using a straightforward ionic cross-linking approach. The primary objective of this technique was to enhance affinity and adsorption capability of SDSCS towards aflatoxins. In this context, physicochemical properties of SDSCS characterized with advanced analytical techniques such as scanning electron microscope (SEM) coupled with energy dispersive X-ray spectroscopy (EDS) and Fourier transform infrared spectroscopy (FT-IR) before and after removal of aflatoxin. In this study, effect of the pH on the adsorption of aflatoxins (6ppb) indicated that the increase in SDSCS concentration from low (0.5) to high (2 %) resulted in an increase of about 80 %, 78 % and 81 % in the adsorption percentage of AFB, AFG, and AFB & AFG, respectively. FT-IR analysis showed the intramolecular interactions of the amine groups of chitosan and sulfate group of SDS formed a stable complex in the removal of aflatoxin that verified with appearance of three new additional peaks at 1323.50, 984.34 and 603.42 cm. Notably, SEM images revealed that the porous SDSCS network was filled with aflatoxin molecules supported with EDS findings. Also, in vitro cytotoxicity assessments demonstrated that SDSCS protected HepG cells against cytotoxic effect caused by aflatoxin (5 µM) in a concentration-dependent manner compared to the control (p<0.01). Collectively, the adsorption mechanism may involve attraction of anionic aflatoxin molecule into the interconnected pores of SDSCS complex with numerous cationic active site via hydrogen bond and van der waals force.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/3fc3aeff9bbd/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/924a2ad108c8/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/73b404e49921/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/34d5cc33c0c3/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/421580dfaec8/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/824118928563/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/3eaad38821dc/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/fe5e6571bbb0/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/4769d5ae6ff3/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/bc140d56c095/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/3fc3aeff9bbd/gr9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/924a2ad108c8/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/73b404e49921/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/34d5cc33c0c3/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/421580dfaec8/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/824118928563/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/3eaad38821dc/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/fe5e6571bbb0/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/4769d5ae6ff3/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/bc140d56c095/gr8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71f7/11650310/3fc3aeff9bbd/gr9.jpg

相似文献

[1]
Physicochemical characterization and cytotoxicity assessment of sodium dodecyl sulfate (SDS) modified chitosan (SDSCS) before and after removal of aflatoxins (AFs) as a potential mycotoxin Binder.

Toxicol Rep. 2024-11-26

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[6]
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[7]
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J Sci Food Agric. 2018-1

[8]
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[9]
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J Chromatogr B Analyt Technol Biomed Life Sci. 2022-11-1

[10]
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本文引用的文献

[1]
Modeling and characterization of lenalidomide-loaded tripolyphosphate-crosslinked chitosan nanoparticles for anticancer drug delivery.

Int J Biol Macromol. 2024-3

[2]
Multi-functional chitosan-based nanoparticles for drug delivery: Recent advanced insight into cancer therapy.

Carbohydr Polym. 2023-9-1

[3]
Review: Application of chitosan and its derivatives in medical materials.

Int J Biol Macromol. 2023-6-15

[4]
Recent developments in improving the emulsifying properties of chitosan.

Int J Biol Macromol. 2023-6-1

[5]
Patentology of chitinous biomaterials. Part II: chitosan.

Carbohydr Polym. 2023-2-1

[6]
Removal of Aflatoxins Using Agro-Waste-Based Materials and Current Characterization Techniques Used for Biosorption Assessment.

Front Vet Sci. 2022-5-16

[7]
Chitosan: A review of molecular structure, bioactivities and interactions with the human body and micro-organisms.

Carbohydr Polym. 2022-4-15

[8]
Chitosan based bioadhesives for biomedical applications: A review.

Carbohydr Polym. 2022-4-15

[9]
Recent advances of chitosan-based nanoparticles for biomedical and biotechnological applications.

Int J Biol Macromol. 2022-4-1

[10]
Chitosan/Sodium Dodecyl Sulfate Complexes for Microencapsulation of Vitamin E and Its Release Profile-Understanding the Effect of Anionic Surfactant.

Pharmaceuticals (Basel). 2021-12-31

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