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Applications of Mycotoxin Biomarkers in Human Biomonitoring for Exposome-Health Studies: Past, Present, and Future
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Metadata
Document Title
Applications of Mycotoxin Biomarkers in Human Biomonitoring for Exposome-Health Studies: Past, Present, and Future
Author
Owolabi I.O., Siwarak K., Greer B., Rajkovic A., Dall’asta C., Karoonuthaisiri N., Uawisetwathana U., Elliott C.T., Petchkongkaew A.
Affiliations
Center of Excellence in Biocatalyst and Sustainable Biotechnology, Department of Biochemistry, Faculty of Science, Chulalongkorn University, Bangkok, 10330, Thailand; National Nanotechnology Center NANOTEC, National Science and Technology Development Agency NSTDA, Pathum Thani, 12120, Thailand; Center of Excellence in Nanomedicine, Department of Anatomy, Faculty of Medicine, Chulalongkorn University, Bangkok, 10330, Thailand; Department of Biochemistry, Center for Translational Medicine, Faculty of Medicine, Khon Kaen University, Khon Kaen, 40002, Thailand; Department of Biochemistry, Faculty of Science, Kasetsart University, Bangkok, 10900, Thailand; Center of Excellence in Biocatalyst and Sustainable Biotechnology, Department of Chemistry, Faculty of Science, Chulalongkorn University, Bangkok, 10330, Thailand; Program in Bioinformatics and Computational Biology, Graduate School, Chulalongkorn University, Bangkok, 10330, Thailand
Type
Article
Source Title
ACS Omega
ISSN
24701343
Year
2024
Open Access
All Open Access, Gold
Publisher
American Chemical Society
DOI
10.1021/acsomega.3c08969
Abstract
Lung cancer is the leading cause of cancer-related deaths worldwide with high incidence rates for new cases. Conventional cisplatin (CDDP) therapy has limitations due to severe side effects from nonspecific targeting. To address this challenge, nanomedicine offers targeted therapies. In this study, cisplatin-loaded calcium citrate nanoparticles conjugated with epidermal growth factor (CaCit@CDDP-EGF NPs) were synthesized. The resulting nanodrug had a size below 350 nm with a cation charge. Based on density functional theory (DFT), the CaCit@CDDP NP model containing two citrates substituted on two chlorides exhibited a favorable binding energy of ?5.42 eV, and the calculated spectrum at 261 nm closely matched the experimental data. CaCit@CDDP-EGF NPs showed higher inhibition rates against EGFR-expressed and mutant carcinoma cells compared to those of cisplatin while displaying lower cytotoxicity to lung fibroblast cells. Integrating in vitro experiments with in silico studies, these nanoparticles hold promise as a novel nanomedicine for targeted therapy in clinical applications. ? 2024 The Authors. Published by American Chemical Society.
License
CC BY-NC-ND
Rights
Authors
Publication Source
WoS