Cargando…
5FU encapsulated polyglycerol sebacate nanoparticles as anti-cancer drug carriers
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 p...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033480/ https://www.ncbi.nlm.nih.gov/pubmed/35478658 http://dx.doi.org/10.1039/d1ra01722e |
_version_ | 1784692899222388736 |
---|---|
author | Sivanesan, Divya Verma, Rama S. Prasad, Edamana |
author_facet | Sivanesan, Divya Verma, Rama S. Prasad, Edamana |
author_sort | Sivanesan, Divya |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9033480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90334802022-04-26 5FU encapsulated polyglycerol sebacate nanoparticles as anti-cancer drug carriers Sivanesan, Divya Verma, Rama S. Prasad, Edamana RSC Adv Chemistry 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. The Royal Society of Chemistry 2021-05-25 /pmc/articles/PMC9033480/ /pubmed/35478658 http://dx.doi.org/10.1039/d1ra01722e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Sivanesan, Divya Verma, Rama S. Prasad, Edamana 5FU encapsulated polyglycerol sebacate nanoparticles as anti-cancer drug carriers |
title | 5FU encapsulated polyglycerol sebacate nanoparticles as anti-cancer drug carriers |
title_full | 5FU encapsulated polyglycerol sebacate nanoparticles as anti-cancer drug carriers |
title_fullStr | 5FU encapsulated polyglycerol sebacate nanoparticles as anti-cancer drug carriers |
title_full_unstemmed | 5FU encapsulated polyglycerol sebacate nanoparticles as anti-cancer drug carriers |
title_short | 5FU encapsulated polyglycerol sebacate nanoparticles as anti-cancer drug carriers |
title_sort | 5fu encapsulated polyglycerol sebacate nanoparticles as anti-cancer drug carriers |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033480/ https://www.ncbi.nlm.nih.gov/pubmed/35478658 http://dx.doi.org/10.1039/d1ra01722e |
work_keys_str_mv | AT sivanesandivya 5fuencapsulatedpolyglycerolsebacatenanoparticlesasanticancerdrugcarriers AT vermaramas 5fuencapsulatedpolyglycerolsebacatenanoparticlesasanticancerdrugcarriers AT prasadedamana 5fuencapsulatedpolyglycerolsebacatenanoparticlesasanticancerdrugcarriers |