Abstract

Subtle changes in the structure of nanoparticles influence their surface tension and corresponding interaction with cells and proteins. Here, the interaction of the single wall carbon nanotube (SWCNT) and multiwall carbon nanotube (MWCNT) with different surface tension with tau protein was evaluated using a variety of techniques including far and near circular dichroism, fluorescence spectroscopy, dynamic light scattering, Zeta potential, and TEM evaluation. Also the cytotoxicity of SWCNT and MWCNT on the PC12 cell line as a model of nervous system cell line was investigated by the MTT, LDH, acridine orange/ethidium bromide staining, flow cytometry, caspase 3 activity, cell and membrane potential assays. It was observed that SWCNT induced more structural changes of tau protein relative to MWCNT/tau protein interaction. It was also revealed that SWCNT and MWCNT impaired the viability and complexity of PC12 cells in different modes of cytotoxicity. Analysis of cellular outcomes indicated that MWCNT in comparison with SWCNT resulted in induction of necrotic modes of cell death, whereas apoptotic modes of cell death were activated in SWCNT-incubated cells. Together these findings suggest that surface tension may be used to determine how nanoparticle structure affects neurotoxicity and protein conformational changes.

Highlights

  • Subtle changes in the structure of nanoparticles influence their surface tension and corresponding interaction with cells and proteins

  • This study was carried out to determine the effects of single wall carbon nanotube (SWCNT) and multiwall carbon nanotube (MWCNT) on tau protein and PC12 cells as targets to investigate the effect of different Carbon nanotubes (CNTs) on nervous system in vitro

  • In this study we have investigated the interaction of SWCNT and MWCNT with tau protein as a model of nervous system protein by far and near UV-circular dichroism (CD) and fluorescence spectroscopy

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Summary

Introduction

Subtle changes in the structure of nanoparticles influence their surface tension and corresponding interaction with cells and proteins. Analysis of cellular outcomes indicated that MWCNT in comparison with SWCNT resulted in induction of necrotic modes of cell death, whereas apoptotic modes of cell death were activated in SWCNT-incubated cells Together these findings suggest that surface tension may be used to determine how nanoparticle structure affects neurotoxicity and protein conformational changes. PC12 cells exhibited key characteristics of dopaminergic neuronal cells, and have been widely used as a model for neuronal cells studies We used this model to investigate the correlation between surface tension of SWCNT and MWCNT and cytotoxicity on PC12 cells as a model of nervous system cell by MTT, LDH, flow cytometry, mitochondrial and cell membrane potential assays. This research can be used to rationally design a nanocarrier for drug delivery design and therapy

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