Synthesis, characterization and In-vitro studies of CNT/Gd 2 O 3 hybrid structure

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Paul, Rima
Chatterjee, Dipanwita
Das Ghosh, Lopamudra
Narayanswamy, Venkatesha
Pratap Singh, Mahander
Agarwal, Manish
Ghosh, Deepshikha
Radhakrishna, Mithun
Sekhar Tiwary, Chandra
Provazník, Valentýna

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Mark

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Elsevier
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Carbon nanotubes have been explored in various fields of science and technology due to their unique properties. However, their toxic nature put limitations to its consideration for the bio-medical applications. In our work, we report the synthesis of paramagnetic CNT/Gd 2 O 3 hybrid nanostructures through easily scalable electrochemical deposition technique. The nanostructure has shown significant longitudinal relaxivity of 18.93 mM 1 s 1 for water protons indicating its possibility to be used as an MRI contrast agent. The in-vitro cytotoxicity test on the normal (HaCaT) and cancerous (HeLa) cells reveal that CNT/Gd 2 O 3 hybrid nanostructure is bio-compatible in comparison to the pure CNTs, which is further supported by our theoretical studies using MD simulations.
Carbon nanotubes have been explored in various fields of science and technology due to their unique properties. However, their toxic nature put limitations to its consideration for the bio-medical applications. In our work, we report the synthesis of paramagnetic CNT/Gd 2 O 3 hybrid nanostructures through easily scalable electrochemical deposition technique. The nanostructure has shown significant longitudinal relaxivity of 18.93 mM 1 s 1 for water protons indicating its possibility to be used as an MRI contrast agent. The in-vitro cytotoxicity test on the normal (HaCaT) and cancerous (HeLa) cells reveal that CNT/Gd 2 O 3 hybrid nanostructure is bio-compatible in comparison to the pure CNTs, which is further supported by our theoretical studies using MD simulations.

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Carbon Trends. 2023, vol. 11, issue 1, p. 1-10.
https://doi.org/10.1016/j.cartre.2023.100272

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en

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Except where otherwised noted, this item's license is described as Creative Commons Attribution 4.0 International
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