Issue 31, 2021, Issue in Progress

5FU encapsulated polyglycerol sebacate nanoparticles as anti-cancer drug carriers

Abstract

The majority of anti-cancer drugs fail to reach clinical trials due to their low water solubility. A biocompatible drug delivery system that encapsulates and efficiently delivers hydrophobic drugs to the target site is the need of the hour. This study addresses the issue by focusing on a polymeric polyglycerol sebacate (PGS) nanoparticles loaded with 5-fluorouracil (5FU), a primary line chemotherapy drug for many types of cancers. The generated nanoparticle (PGS-NP) was biocompatible and had minimal cytotoxicity against the MDA-MB-231 and A549 cell lines, even at a high concentration of 100 μg mL−1. The cell viability post treatment with PGS nanoparticles encapsulated with 5FU (PGS-5FU) decreased to as low as around 40% whereas, in the case of treatment with 5FU, the viability percentage increased. The nanoparticles also showed controlled drug release when encapsulated with 5FU. This striking observation suggested that these nanoparticles can improve the efficacy of drug delivery to tumor sites. Apoptosis assay and caspase-3 activity quantification supported these data wherein PGS-5FU treatment showed almost three times caspase-3 activity as compared to control cells. Additionally, throughout all the experiments, MDA-MB-231 cells were more sensitive to PGS-5FU than A549 cells, indicating that these nanoparticles are ideal for breast cancer treatment. In summary, 5FU encapsulated PGS nanoparticles are a potential drug carrier to deliver 5FU efficiently to cancer cells.

Graphical abstract: 5FU encapsulated polyglycerol sebacate nanoparticles as anti-cancer drug carriers

Supplementary files

Article information

Article type
Paper
Submitted
04 Mar 2021
Accepted
10 May 2021
First published
25 May 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 18984-18993

5FU encapsulated polyglycerol sebacate nanoparticles as anti-cancer drug carriers

D. Sivanesan, R. S. Verma and E. Prasad, RSC Adv., 2021, 11, 18984 DOI: 10.1039/D1RA01722E

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