{"title":"Novel synthesized, characterization and <i>in vitro</i> toxicological evaluation of amino acid-based-cerium oxide nanoparticles (CeO<sub>2</sub> NPs).","authors":"Sedanur Güngör, Buket Bakan","doi":"10.1080/01480545.2025.2484461","DOIUrl":null,"url":null,"abstract":"<p><p>Surface modifications improve the properties of nanomaterials and make them more appropriate for various applications. Various materials are used for surface modification of cerium nanoparticles (CeO<sub>2</sub> NPs); however, there is no modification process of cerium with glutamic acid. This study focused on the preparation of L-glutamic acid-coated CeO<sub>2</sub> NPs and reveal its potential toxicity depending on the characteristic properties. Characterization analysis was performed by Transmission electron microscopy (TEM), Fourier transform infrared (FT-IR), ZETA sizer/potential and X-ray diffraction (XRD). <i>In vitro</i> toxicities of CeO<sub>2</sub> NPs and Glu-CeO<sub>2</sub> NPs were investigated by using WST-1 (2-(4-iodophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfophenyl)-2H-tetrazolium, monosodium salt), hemolysis and HET-CAM (Hen's egg-chorioallantoic membrane) tests. Both NPs-group were determined to be non- cytotoxic on L929 and MCF-10A cell lines, but slightly decrease the viability of A549 and MCF-7 cells after 24 exposure. Glu-CeO<sub>2</sub> NPs increased cell migration in MCF-10A cell line but inhibited in A549 cells. In contrast to CeO<sub>2</sub> NPs, Glu-CeO<sub>2</sub> NPs reduced oxidative stress and hemolysis rate. CeO<sub>2</sub> NP was caused lysis after 0.5nd min, while Glu-CeO<sub>2</sub> NPs didn't exhibit any irritation effect. This is the first report on the synthesis of Glu-CeO<sub>2</sub> NPs. This formulation may be used in drug delivery systems due to its potential to reduce toxicity of CeO<sub>2</sub> NPs.</p>","PeriodicalId":11333,"journal":{"name":"Drug and Chemical Toxicology","volume":" ","pages":"1-12"},"PeriodicalIF":2.1000,"publicationDate":"2025-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Drug and Chemical Toxicology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/01480545.2025.2484461","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Surface modifications improve the properties of nanomaterials and make them more appropriate for various applications. Various materials are used for surface modification of cerium nanoparticles (CeO2 NPs); however, there is no modification process of cerium with glutamic acid. This study focused on the preparation of L-glutamic acid-coated CeO2 NPs and reveal its potential toxicity depending on the characteristic properties. Characterization analysis was performed by Transmission electron microscopy (TEM), Fourier transform infrared (FT-IR), ZETA sizer/potential and X-ray diffraction (XRD). In vitro toxicities of CeO2 NPs and Glu-CeO2 NPs were investigated by using WST-1 (2-(4-iodophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfophenyl)-2H-tetrazolium, monosodium salt), hemolysis and HET-CAM (Hen's egg-chorioallantoic membrane) tests. Both NPs-group were determined to be non- cytotoxic on L929 and MCF-10A cell lines, but slightly decrease the viability of A549 and MCF-7 cells after 24 exposure. Glu-CeO2 NPs increased cell migration in MCF-10A cell line but inhibited in A549 cells. In contrast to CeO2 NPs, Glu-CeO2 NPs reduced oxidative stress and hemolysis rate. CeO2 NP was caused lysis after 0.5nd min, while Glu-CeO2 NPs didn't exhibit any irritation effect. This is the first report on the synthesis of Glu-CeO2 NPs. This formulation may be used in drug delivery systems due to its potential to reduce toxicity of CeO2 NPs.
期刊介绍:
Drug and Chemical Toxicology publishes full-length research papers, review articles and short communications that encompass a broad spectrum of toxicological data surrounding risk assessment and harmful exposure. Manuscripts are considered according to their relevance to the journal.
Topics include both descriptive and mechanics research that illustrates the risk assessment implications of exposure to toxic agents. Examples of suitable topics include toxicological studies, which are structural examinations on the effects of dose, metabolism, and statistical or mechanism-based approaches to risk assessment. New findings and methods, along with safety evaluations, are also acceptable. Special issues may be reserved to publish symposium summaries, reviews in toxicology, and overviews of the practical interpretation and application of toxicological data.