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Comparison Direct Synthesis of Hyaluronic Acid-Based Carbon Nanodots as Dual Active Targeting and Imaging of HeLa Cancer Cells

[Image: see text] The present study explores the potential of carbon nanodots (CDs) synthesized from hyaluronic acid using microwave-assisted and furnace-assisted methods as bioimaging agents for cancer cells. The investigation on the effect of microwave-assisted and furnace-assisted times (2 min an...

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Autores principales: Aung, Yu-Yu, Wibrianto, Aswandi, Sianturi, Jefry S., Ulfa, Desita K., Sakti, Satya. C. W., Irzaman, Irzaman, Yuliarto, Brian, Chang, Jia-yaw, Kwee, Yaung, Fahmi, Mochamad Z.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8158841/
https://www.ncbi.nlm.nih.gov/pubmed/34056478
http://dx.doi.org/10.1021/acsomega.1c01287
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author Aung, Yu-Yu
Wibrianto, Aswandi
Sianturi, Jefry S.
Ulfa, Desita K.
Sakti, Satya. C. W.
Irzaman, Irzaman
Yuliarto, Brian
Chang, Jia-yaw
Kwee, Yaung
Fahmi, Mochamad Z.
author_facet Aung, Yu-Yu
Wibrianto, Aswandi
Sianturi, Jefry S.
Ulfa, Desita K.
Sakti, Satya. C. W.
Irzaman, Irzaman
Yuliarto, Brian
Chang, Jia-yaw
Kwee, Yaung
Fahmi, Mochamad Z.
author_sort Aung, Yu-Yu
collection PubMed
description [Image: see text] The present study explores the potential of carbon nanodots (CDs) synthesized from hyaluronic acid using microwave-assisted and furnace-assisted methods as bioimaging agents for cancer cells. The investigation on the effect of microwave-assisted and furnace-assisted times (2 min and 2 h) on determining CD character is dominantly discussed. Various CDs, such as HA-P1 and HA-P2 were, respectively, synthesized through the furnace-assisted method at 270 °C for 2 min and 2 h, whereas HA-M1 and HA-M2 were synthesized with the microwave-assisted method for 2 min and 2 h, respectively. Overall, various CDs were produced with an average diameter, with the maximum absorption of HA-P1, HA-P2, HA-M1, and HA-M2 at 234, 238, 221, and 217 nm, respectively. The photoluminescence spectra of these CDs showed particular emissions at 320 nm and excitation wavelengths from 340 to 400 nm. Several characterizations such as X-ray photoelectron spectroscopy, Fourier-transform infrared spectroscopy, X-ray diffraction, and Raman spectroscopy reveal the CD properties such as amorphous structures, existence of D bands and G bands, and hydrophilic property supported with hydroxyl and carboxyl groups. The quantum yields of HA-M1, HA-M2, HA-P1, and HA-P2 were 12, 7, 9, and 23%, respectively. The cytotoxicity and in vitro activity were verified by a cell counting kit-8 assay and confocal laser scanning microscopy, which show a low toxicity with the percentage of living cells above 80%.
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spelling pubmed-81588412021-05-28 Comparison Direct Synthesis of Hyaluronic Acid-Based Carbon Nanodots as Dual Active Targeting and Imaging of HeLa Cancer Cells Aung, Yu-Yu Wibrianto, Aswandi Sianturi, Jefry S. Ulfa, Desita K. Sakti, Satya. C. W. Irzaman, Irzaman Yuliarto, Brian Chang, Jia-yaw Kwee, Yaung Fahmi, Mochamad Z. ACS Omega [Image: see text] The present study explores the potential of carbon nanodots (CDs) synthesized from hyaluronic acid using microwave-assisted and furnace-assisted methods as bioimaging agents for cancer cells. The investigation on the effect of microwave-assisted and furnace-assisted times (2 min and 2 h) on determining CD character is dominantly discussed. Various CDs, such as HA-P1 and HA-P2 were, respectively, synthesized through the furnace-assisted method at 270 °C for 2 min and 2 h, whereas HA-M1 and HA-M2 were synthesized with the microwave-assisted method for 2 min and 2 h, respectively. Overall, various CDs were produced with an average diameter, with the maximum absorption of HA-P1, HA-P2, HA-M1, and HA-M2 at 234, 238, 221, and 217 nm, respectively. The photoluminescence spectra of these CDs showed particular emissions at 320 nm and excitation wavelengths from 340 to 400 nm. Several characterizations such as X-ray photoelectron spectroscopy, Fourier-transform infrared spectroscopy, X-ray diffraction, and Raman spectroscopy reveal the CD properties such as amorphous structures, existence of D bands and G bands, and hydrophilic property supported with hydroxyl and carboxyl groups. The quantum yields of HA-M1, HA-M2, HA-P1, and HA-P2 were 12, 7, 9, and 23%, respectively. The cytotoxicity and in vitro activity were verified by a cell counting kit-8 assay and confocal laser scanning microscopy, which show a low toxicity with the percentage of living cells above 80%. American Chemical Society 2021-05-11 /pmc/articles/PMC8158841/ /pubmed/34056478 http://dx.doi.org/10.1021/acsomega.1c01287 Text en © 2021 The Authors. Published by American Chemical Society Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Aung, Yu-Yu
Wibrianto, Aswandi
Sianturi, Jefry S.
Ulfa, Desita K.
Sakti, Satya. C. W.
Irzaman, Irzaman
Yuliarto, Brian
Chang, Jia-yaw
Kwee, Yaung
Fahmi, Mochamad Z.
Comparison Direct Synthesis of Hyaluronic Acid-Based Carbon Nanodots as Dual Active Targeting and Imaging of HeLa Cancer Cells
title Comparison Direct Synthesis of Hyaluronic Acid-Based Carbon Nanodots as Dual Active Targeting and Imaging of HeLa Cancer Cells
title_full Comparison Direct Synthesis of Hyaluronic Acid-Based Carbon Nanodots as Dual Active Targeting and Imaging of HeLa Cancer Cells
title_fullStr Comparison Direct Synthesis of Hyaluronic Acid-Based Carbon Nanodots as Dual Active Targeting and Imaging of HeLa Cancer Cells
title_full_unstemmed Comparison Direct Synthesis of Hyaluronic Acid-Based Carbon Nanodots as Dual Active Targeting and Imaging of HeLa Cancer Cells
title_short Comparison Direct Synthesis of Hyaluronic Acid-Based Carbon Nanodots as Dual Active Targeting and Imaging of HeLa Cancer Cells
title_sort comparison direct synthesis of hyaluronic acid-based carbon nanodots as dual active targeting and imaging of hela cancer cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8158841/
https://www.ncbi.nlm.nih.gov/pubmed/34056478
http://dx.doi.org/10.1021/acsomega.1c01287
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