open access

Vol 5, No 1 (2020)
Original article
Published online: 2019-12-19
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Possibilities in the application of solid lipid nanoparticles in combination with 5-fluorouracil to overcome the drugresistance of non-small cell lung cancer cell line A549

Wioletta Zielińska12, Agnieszka Nawrocka2, Maciej Rydzkowski2, Anna Kokocha2, Karolina Matulewicz2, Marta Hałas-Wiśniewska12, Magdalena Izdebska12
·
Medical Research Journal 2020;5(1):1-8.
Affiliations
  1. Department of Histology and Embryology, Faculty of Medicine, Collegium Medicum in Bydgoszcz Nicolaus Copernicus University in Toruń, 24 Karłowicza St., 85-092 Bydgoszcz, Poland
  2. Students research group of Cell Biology and Ultrastructure at Department of Histology and Embryology, Nicolaus Copernicus University in Toruń, Collegium Medicum in Bydgoszcz, Poland., 24 Karłowicza St., 85-092 Bydgoszcz, Poland

open access

Vol 5, No 1 (2020)
ORIGINAL ARTICLES
Published online: 2019-12-19

Abstract

Introduction: Multidrug resistance of non-small cell lung cancer cells is associated with a high percentage
of therapeutic failures. The aim of this study was to assess the ability of solid lipid nanoparticles as a
transporter of the conventionally used cytostatic (5-fluorouracil) to overcome the resistance of A549 cells.

Material and methods: MTT assay was used to assess the differences in viability of cells treated with
5-fluorouracil alone or in combination with different types of solid lipid nanoparticles. Type of cell death
and distribution of cell cycle phases were evaluated using flow cytometry.

Results: The use of nanoparticles as a 5-fluorouracil transporter reduced the viability of A549 cells to a
greater extent than the cytostatic alone. This was mainly due to the increase in apoptosis, but also necrosis
and cell cycle arrest.

Conclusion: Our results indicate the great potential of nanotechnology in the treatment of non-small cell
lung cancer. By using nanoparticles, it is possible to sensitise tumour cells to cytostatics to which they
are normally resistant. In addition, literature data confirm the safety of solid lipid nanoparticle application.

Abstract

Introduction: Multidrug resistance of non-small cell lung cancer cells is associated with a high percentage
of therapeutic failures. The aim of this study was to assess the ability of solid lipid nanoparticles as a
transporter of the conventionally used cytostatic (5-fluorouracil) to overcome the resistance of A549 cells.

Material and methods: MTT assay was used to assess the differences in viability of cells treated with
5-fluorouracil alone or in combination with different types of solid lipid nanoparticles. Type of cell death
and distribution of cell cycle phases were evaluated using flow cytometry.

Results: The use of nanoparticles as a 5-fluorouracil transporter reduced the viability of A549 cells to a
greater extent than the cytostatic alone. This was mainly due to the increase in apoptosis, but also necrosis
and cell cycle arrest.

Conclusion: Our results indicate the great potential of nanotechnology in the treatment of non-small cell
lung cancer. By using nanoparticles, it is possible to sensitise tumour cells to cytostatics to which they
are normally resistant. In addition, literature data confirm the safety of solid lipid nanoparticle application.

Get Citation

Keywords

A549, solid lipid nanoparticles, 5-fluorouracil, drug-resistance, nanotechnology

About this article
Title

Possibilities in the application of solid lipid nanoparticles in combination with 5-fluorouracil to overcome the drugresistance of non-small cell lung cancer cell line A549

Journal

Medical Research Journal

Issue

Vol 5, No 1 (2020)

Article type

Original article

Pages

1-8

Published online

2019-12-19

Page views

634

Article views/downloads

894

DOI

10.5603/MRJ.a2019.0037

Bibliographic record

Medical Research Journal 2020;5(1):1-8.

Keywords

A549
solid lipid nanoparticles
5-fluorouracil
drug-resistance
nanotechnology

Authors

Wioletta Zielińska
Agnieszka Nawrocka
Maciej Rydzkowski
Anna Kokocha
Karolina Matulewicz
Marta Hałas-Wiśniewska
Magdalena Izdebska

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