| Literature DB >> 27013133 |
Muddasarul Hoda1, Sankar Pajaniradje1, Garima Shakya1, Kumaravel Mohankumar1, Rukkumani Rajagopalan2.
Abstract
There is an emerging trend to restudy known drugs for their anti-cancer potential. One such anti-alcoholic drug, disulfiram, with significant anti-cancer potential was studied for its efficacy against Hep3B cell lines, an in vitro model of hepatocellular carcinoma. Simultaneously, we intended to study the effect of polysorbate 80-stabilized PLGA nanoparticles and its DSF-loaded counterpart. Cell and nuclear staining, comet assay, flow cytometry and Western blots were performed. Results suggest that cell proliferation was inhibited by DSF and its PLGA nanoparticles through cell cycle arrest, triggering activation of apoptotic pathways that culminates with cell death. DSF loaded nanoparticles when compared with free DSF, showed significantly lesser effect due to its sustained drug-releasing property, while empty nanoparticles showed negligible influence on Hep3B cells. Our results suggest that DSF alone contributes to cell death, while polysorbate 80-stabilized PLGA nanoparticles show sustained drug release patterns that would potentially lower dosage regimens.Entities:
Keywords: Apoptosis; Biodegradable nanoparticles; Cancer; Disulfiram; PLGA
Mesh:
Substances:
Year: 2016 PMID: 27013133 DOI: 10.1016/j.nano.2016.02.013
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307