4.7 Article

Microwave-irradiation-assisted hybrid chemical approach for titanium dioxide nanoparticle synthesis: microbial and cytotoxicological evaluation

Journal

ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
Volume 23, Issue 12, Pages 12287-12302

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s11356-016-6440-8

Keywords

Microwave irradiation; Chemical synthesis; Titanium dioxide nanoparticle; Toxicity; Microbes; Cell lines

Funding

  1. Department of Biotechnology (DBT, India) [BT/PR10414/PFN/20/961/2014]
  2. Veer Kunwar Singh Memorial Trust, Chapra, Bihar, India [VKSMT/SN/NFNA/0011]

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Titanium dioxide nanoparticles (TNPs) are widely used in the pharmaceutical and cosmetics industries. It is used for protection against UV exposure due to its light-scattering properties and high refractive index. Though TNPs are increasingly used, the synthesis of TNPs is tedious and time consuming; therefore, in the present study, microwave-assisted hybrid chemical approach was used for TNP synthesis. In the present study, we demonstrated that TNPs can be synthesized only in 2.5 h; however, the commonly used chemical approach using muffle furnace takes 5 h. The activity of TNP depends on the synthetic protocol; therefore, the present study also determined the effect of microwave-assisted hybrid chemical approach synthetic protocol on microbial and cytotoxicity. The results showed that TNP has the best antibacterial activity in decreasing order from Escherichia coli, Bacillus subtilis, and Staphylococcus aureus. The IC50 values of TNP for HCT116 and A549 were found to be 6.43 and 6.04 ppm, respectively. Cell death was also confirmed from trypan blue exclusion assay and membrane integrity loss was observed. Therefore, the study determines that the microwave-assisted hybrid chemical approach is time-saving; hence, this technique can be upgraded from lab scale to industrial scale via pilot plant scale. Moreover, it is necessary to find the mechanism of action at the molecular level to establish the reason for greater bacterial and cytotoxicological toxicity.

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