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The response effect of pheochromocytoma (PC12) cell lines to oxidized multi-walled carbon nanotubes (o-MWCMTs)
Background: The applications of oxidized carbon nanotubes (o-CNTs) have shown potentials in novel drug delivery including the brain which is usually a challenge. This underscores the importance to study its potential toxic effect in animals. Despite being a promising tool for biomedical applications...
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Published in: | African health sciences 2013-01, Vol.13 (4), p.947-954 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Background: The applications of oxidized carbon nanotubes (o-CNTs) have
shown potentials in novel drug delivery including the brain which is
usually a challenge. This underscores the importance to study its
potential toxic effect in animals. Despite being a promising tool for
biomedical applications little is known about the safety of drugs in
treating brain diseases. The toxicity of oxidized multi-walled carbon
nanotubes (o-MWCNTs) are of utmost concern and in most in-vitro studies
conducted so far are on dendritic cell (DC) lines with limited data on
PC12 cell lines. Objectives: We focused on the effect of o-MWCNTs in
PC12 cells in vitro: a common model cell for neurotoxicity. Methods:
The pristine multi-walled carbon nanotubes (p-MWCNTs) were produced by
the swirled floating catalytic chemical vapour deposition method
(SFCCVD). The p-MWCNTs were then oxidized using purified H2SO4/HNO3
(3:1v/v) and 30% HNO3 acids to produce o-MWCNTs. The
Brunauer-Emmett-Teller (BET), transmission electron microscopy
(TEM),Scanning electron microscopy (SEM), thermogravimetric analyser
(TGA) and Raman spectroscopy techniques were used to characterize the
MWCNTs. The PC12 cells were cultured in RPMI medium containing
concentrations of o-MWCNTs ranging from 50 to 200 μg/ml. Results:
The o-MWCNTs demonstrated slight cytotoxicity at short time period to
PC12 neuronal cells whilst at longer time period, no significant (p
> 0.05) toxicity was observed due to cell recovery. Conclusion: In
conclusion, the o-MWCNTs did not affect the growth rate and viability
of the PC12 cells due to lack of considerable toxicity in the cells
during the observed time period but further investigations are required
to determine cell recovery mechanism. |
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ISSN: | 1680-6905 1729-0503 1680-6905 |
DOI: | 10.4314/ahs.v13i4.13 |