4.6 Article

Niclosamide loaded biodegradable chitosan nanocargoes: an in vitro study for potential application in cancer therapy

Journal

ROYAL SOCIETY OPEN SCIENCE
Volume 4, Issue 11, Pages -

Publisher

ROYAL SOC
DOI: 10.1098/rsos.170611

Keywords

chitosan; niclosamide; cell cycle; semi-quantitative reverse transcription polymerase chain reaction; apoptosis

Funding

  1. Ministry of Human Resource Development (MHRD), Government of India [MHR-01-23-200-328]
  2. Women Scientist Scheme (WOS-A), Department of Science and Technology, Government of India [SR/WOS-A/LS-1224/2015]
  3. University Grants Commission (UGC), Government of India

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Chitosan nanoparticles can advance the pharmacological and therapeutic properties of chemotherapeutic agents by controlling release rates and targeted delivery process, which eliminates the limitations of conventional anti-cancer therapies and they are also safe as well as cost-effective. The aim of present study is to explore the anti-tumour effect of niclosamide in lung and breast cancer cell lines using biocompatible and biodegradable carrier where nanoparticles loaded with hydrophobic drug (niclosamide) were synthesized, characterized and applied as a stable anti-cancer agent. Niclosamide loaded chitosan nanoparticles (Nic-Chi Np's) of size approximately 100-120nm in diameter containing hydrophobic anti-cancer drug, i.e. niclosamide, were prepared. Physico-chemical characterization confirms that the prepared nanoparticles are spherical, monodispersed and stable in aqueous systems. The therapeutic efficacy of Nic-Chi Np's was evaluated against breast cancer cell line (MCF-7) and human lung cancer cell line (A549). MTT assay reveals the cell viability of the prepared Nic-Chi Np's against A549 and MCF-7 cells and obtained an IC50 value of 8.75 mu M and 7.5 mu M, respectively. Acridine orange/ethidium bromide dual staining results verified the loss of the majority of the cells by apoptosis. Flow cytometer analysis quantified the generation of intracellular reactive oxygen species (ROS) and signified that exposure to a higher concentration (2xIC(50)) of Nic-Chi Np's resulted in elevated ROS generation. Notably, Nic-Chi Np treatment showed more apoptosis and cell death in MCF-7 as compared to A549. Further, the remarkable induction of apoptosis by Nic-Chi Np's was confirmed by semi-quantitative reverse transcription polymerase chain reaction, scanning electron

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