Comparative cytotoxic effect of citrate-capped gold nanoparticles with different sizes on noncancerous and cancerous cell lines
Gold nanoparticles (GNPs) have properties that can be applied to the diagnosis and therapies of cancer, improving both the control and efficiency of treatment. Therefore, the aim of this study was to synthesize and characterize GNPs of different sizes and evaluate their cytotoxicity in human erythro...
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Published in: | Journal of nanoparticle research : an interdisciplinary forum for nanoscale science and technology Vol. 22; no. 6 |
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Main Authors: | , , , , , , , , , , , |
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Language: | English |
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01-06-2020
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Abstract | Gold nanoparticles (GNPs) have properties that can be applied to the diagnosis and therapies of cancer, improving both the control and efficiency of treatment. Therefore, the aim of this study was to synthesize and characterize GNPs of different sizes and evaluate their cytotoxicity in human erythrocytes, murine fibroblasts (NIH3T3), human cervix carcinoma cells (HeLa), and melanoma cells (B16F10). GNPs were successfully synthesized by the Turkevich method, to obtain citrate-capped GNPs with different sizes (10, 20, and 30 nm). Transmission electron microscopy images showed GNPs with spherical/near-spherical morphology and their sizes were confirmed by ultraviolet-visible spectroscopy analysis. FTIR and XRD spectra confirmed that the citrate-capped GNPs have been formed with appearance of peakscharacteristic. Cytotoxicity studies showed that the 20 nm GNPs exerted lower cytotoxic effects on noncancerous cells than other GNPs and presented a higher cytotoxic effect on the HeLa cells. In contrast, when GNPs were incubated with B16F10 cells, the 10 nm GNPs were more cytotoxic than the 20 and 30 nm GNPs. HeLa cells were more sensitive (IC
50
2.1 μg/mL) to treatment with GNPs than B16F10 cells (IC
50
> 70 μg/mL). Therefore, this study demonstrated that the physicochemical properties, concentration, and cell type used were limiting factors for the cytotoxic effect of GNPs. Lastly, these results confirm the need for future studies to evaluate cellular uptake, death mechanism, and other biochemical parameters required to develop novel cancer therapies.
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AbstractList | Gold nanoparticles (GNPs) have properties that can be applied to the diagnosis and therapies of cancer, improving both the control and efficiency of treatment. Therefore, the aim of this study was to synthesize and characterize GNPs of different sizes and evaluate their cytotoxicity in human erythrocytes, murine fibroblasts (NIH3T3), human cervix carcinoma cells (HeLa), and melanoma cells (B16F10). GNPs were successfully synthesized by the Turkevich method, to obtain citrate-capped GNPs with different sizes (10, 20, and 30 nm). Transmission electron microscopy images showed GNPs with spherical/near-spherical morphology and their sizes were confirmed by ultraviolet-visible spectroscopy analysis. FTIR and XRD spectra confirmed that the citrate-capped GNPs have been formed with appearance of peakscharacteristic. Cytotoxicity studies showed that the 20 nm GNPs exerted lower cytotoxic effects on noncancerous cells than other GNPs and presented a higher cytotoxic effect on the HeLa cells. In contrast, when GNPs were incubated with B16F10 cells, the 10 nm GNPs were more cytotoxic than the 20 and 30 nm GNPs. HeLa cells were more sensitive (IC
50
2.1 μg/mL) to treatment with GNPs than B16F10 cells (IC
50
> 70 μg/mL). Therefore, this study demonstrated that the physicochemical properties, concentration, and cell type used were limiting factors for the cytotoxic effect of GNPs. Lastly, these results confirm the need for future studies to evaluate cellular uptake, death mechanism, and other biochemical parameters required to develop novel cancer therapies.
Graphical abstract Gold nanoparticles (GNPs) have properties that can be applied to the diagnosis and therapies of cancer, improving both the control and efficiency of treatment. Therefore, the aim of this study was to synthesize and characterize GNPs of different sizes and evaluate their cytotoxicity in human erythrocytes, murine fibroblasts (NIH3T3), human cervix carcinoma cells (HeLa), and melanoma cells (B16F10). GNPs were successfully synthesized by the Turkevich method, to obtain citrate-capped GNPs with different sizes (10, 20, and 30 nm). Transmission electron microscopy images showed GNPs with spherical/near-spherical morphology and their sizes were confirmed by ultraviolet-visible spectroscopy analysis. FTIR and XRD spectra confirmed that the citrate-capped GNPs have been formed with appearance of peakscharacteristic. Cytotoxicity studies showed that the 20 nm GNPs exerted lower cytotoxic effects on noncancerous cells than other GNPs and presented a higher cytotoxic effect on the HeLa cells. In contrast, when GNPs were incubated with B16F10 cells, the 10 nm GNPs were more cytotoxic than the 20 and 30 nm GNPs. HeLa cells were more sensitive (IC50 2.1 μg/mL) to treatment with GNPs than B16F10 cells (IC50 > 70 μg/mL). Therefore, this study demonstrated that the physicochemical properties, concentration, and cell type used were limiting factors for the cytotoxic effect of GNPs. Lastly, these results confirm the need for future studies to evaluate cellular uptake, death mechanism, and other biochemical parameters required to develop novel cancer therapies. |
ArticleNumber | 133 |
Author | Freitas, Mauricio Lawrence Feuser, Paulo Emilio Machado-de-Ávila, Ricardo Andrez dos Santos Pedroso Fidelis, Giulia Possato, Jonathann Corrêa Galvani, Nathalia Coral Fagundes, Mírian Ívens Vechia, Indiani Conti Della de Araújo, Pedro Henrique Hermes Steiner, Bethina Trevisol Rigo, Flávia Karine Ronchi, Jonatha Moretto |
Author_xml | – sequence: 1 givenname: Indiani Conti Della surname: Vechia fullname: Vechia, Indiani Conti Della organization: Postgraduate Program in Health Science, University of the Extreme South Santa Catarina – sequence: 2 givenname: Bethina Trevisol surname: Steiner fullname: Steiner, Bethina Trevisol organization: Postgraduate Program in Health Science, University of the Extreme South Santa Catarina – sequence: 3 givenname: Mauricio Lawrence surname: Freitas fullname: Freitas, Mauricio Lawrence organization: Postgraduate Program in Health Science, University of the Extreme South Santa Catarina – sequence: 4 givenname: Giulia surname: dos Santos Pedroso Fidelis fullname: dos Santos Pedroso Fidelis, Giulia organization: Postgraduate Program in Health Science, University of the Extreme South Santa Catarina – sequence: 5 givenname: Nathalia Coral surname: Galvani fullname: Galvani, Nathalia Coral organization: Postgraduate Program in Health Science, University of the Extreme South Santa Catarina – sequence: 6 givenname: Jonatha Moretto surname: Ronchi fullname: Ronchi, Jonatha Moretto organization: Postgraduate Program in Health Science, University of the Extreme South Santa Catarina – sequence: 7 givenname: Jonathann Corrêa surname: Possato fullname: Possato, Jonathann Corrêa organization: Postgraduate Program in Health Science, University of the Extreme South Santa Catarina – sequence: 8 givenname: Mírian Ívens surname: Fagundes fullname: Fagundes, Mírian Ívens organization: Postgraduate Program in Health Science, University of the Extreme South Santa Catarina – sequence: 9 givenname: Flávia Karine surname: Rigo fullname: Rigo, Flávia Karine organization: Postgraduate Program in Health Science, University of the Extreme South Santa Catarina – sequence: 10 givenname: Paulo Emilio surname: Feuser fullname: Feuser, Paulo Emilio organization: Postgraduate Program in Health Science, University of the Extreme South Santa Catarina, Department of Chemical Engineering and Food Engineering, Federal University of Santa Catarina – sequence: 11 givenname: Pedro Henrique Hermes surname: de Araújo fullname: de Araújo, Pedro Henrique Hermes organization: Department of Chemical Engineering and Food Engineering, Federal University of Santa Catarina – sequence: 12 givenname: Ricardo Andrez surname: Machado-de-Ávila fullname: Machado-de-Ávila, Ricardo Andrez email: r_andrez@unesc.net organization: Postgraduate Program in Health Science, University of the Extreme South Santa Catarina |
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Snippet | Gold nanoparticles (GNPs) have properties that can be applied to the diagnosis and therapies of cancer, improving both the control and efficiency of treatment.... |
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SubjectTerms | Cancer Cervical carcinoma Cervix Characterization and Evaluation of Materials Chemistry and Materials Science Citric acid Cytotoxicity Erythrocytes Fibroblasts Gold Image transmission Inorganic Chemistry Lasers Limiting factors Materials Science Melanoma Morphology Nanoparticles Nanotechnology Optical Devices Optics Photonics Physical Chemistry Physicochemical properties Research Paper Spectrum analysis Synthesis Toxicity Transmission electron microscopy |
Title | Comparative cytotoxic effect of citrate-capped gold nanoparticles with different sizes on noncancerous and cancerous cell lines |
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