Genotoxic evaluation of polymeric nanoparticles

An important strategy for optimizing the therapeutic efficacy of many conventional drugs is the development of polymeric nanoparticles (NPs), as it may expand their activities, reduce their toxicity, increase their bioactivity and improve biodistribution. The main objective of this study was to ev...

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Main Author: Tamara Iglesias Alonso
Format: Article
Language:English
Published: Frontiers Media S.A. 2015-06-01
Series:Frontiers in Genetics
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/conf.fgene.2015.01.00011/full
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spelling doaj-3e80ac0b69674b3bb80c72269c2f592e2020-11-24T22:01:58ZengFrontiers Media S.A.Frontiers in Genetics1664-80212015-06-01610.3389/conf.fgene.2015.01.00011149832Genotoxic evaluation of polymeric nanoparticlesTamara Iglesias Alonso0University of NavarraAn important strategy for optimizing the therapeutic efficacy of many conventional drugs is the development of polymeric nanoparticles (NPs), as it may expand their activities, reduce their toxicity, increase their bioactivity and improve biodistribution. The main objective of this study was to evaluate the genotoxicity of 8 different poly (anhydride) NPs designed for the oral administration of therapeutic compounds by using the comet assay in combination with the enzyme formamidopypiridine DNA-glycosylase (FPG). Furthermore, the mitogen capacity of the NPs was evaluated by the proliferation assay. All NPs were tested at four concentrations (0, 0.5, 1 and 2 mg/mL) in Caco-2 cells after 3 hours of treatment while selected NPs were also tested after 24 h. The comet assay was performed immediately after the treatment and cell proliferation was assessed by counting the treated cells after their incubation at 37 °C for 48h. Cells treated with 1 µM of the photosensitizer Ro 19-8022 plus 5 min of light, as well as cells treated with 100 µM H2O2 were included as positive controls in all the experiments. All NPs studied did not result in any increase in the frequency of strand breaks or alkali-labile sites in Caco-2 cells but they induced a slight concentration-dependent increase in net FPG sensitive sites (oxidized and/or alkylated bases). Furthermore, treated cells did not show changes in levels of proliferation in comparison with the negative control.http://journal.frontiersin.org/Journal/10.3389/conf.fgene.2015.01.00011/fullComet Assayoral administrationpolymeric nanoparticlesBiological barriersProliferation assay
collection DOAJ
language English
format Article
sources DOAJ
author Tamara Iglesias Alonso
spellingShingle Tamara Iglesias Alonso
Genotoxic evaluation of polymeric nanoparticles
Frontiers in Genetics
Comet Assay
oral administration
polymeric nanoparticles
Biological barriers
Proliferation assay
author_facet Tamara Iglesias Alonso
author_sort Tamara Iglesias Alonso
title Genotoxic evaluation of polymeric nanoparticles
title_short Genotoxic evaluation of polymeric nanoparticles
title_full Genotoxic evaluation of polymeric nanoparticles
title_fullStr Genotoxic evaluation of polymeric nanoparticles
title_full_unstemmed Genotoxic evaluation of polymeric nanoparticles
title_sort genotoxic evaluation of polymeric nanoparticles
publisher Frontiers Media S.A.
series Frontiers in Genetics
issn 1664-8021
publishDate 2015-06-01
description An important strategy for optimizing the therapeutic efficacy of many conventional drugs is the development of polymeric nanoparticles (NPs), as it may expand their activities, reduce their toxicity, increase their bioactivity and improve biodistribution. The main objective of this study was to evaluate the genotoxicity of 8 different poly (anhydride) NPs designed for the oral administration of therapeutic compounds by using the comet assay in combination with the enzyme formamidopypiridine DNA-glycosylase (FPG). Furthermore, the mitogen capacity of the NPs was evaluated by the proliferation assay. All NPs were tested at four concentrations (0, 0.5, 1 and 2 mg/mL) in Caco-2 cells after 3 hours of treatment while selected NPs were also tested after 24 h. The comet assay was performed immediately after the treatment and cell proliferation was assessed by counting the treated cells after their incubation at 37 °C for 48h. Cells treated with 1 µM of the photosensitizer Ro 19-8022 plus 5 min of light, as well as cells treated with 100 µM H2O2 were included as positive controls in all the experiments. All NPs studied did not result in any increase in the frequency of strand breaks or alkali-labile sites in Caco-2 cells but they induced a slight concentration-dependent increase in net FPG sensitive sites (oxidized and/or alkylated bases). Furthermore, treated cells did not show changes in levels of proliferation in comparison with the negative control.
topic Comet Assay
oral administration
polymeric nanoparticles
Biological barriers
Proliferation assay
url http://journal.frontiersin.org/Journal/10.3389/conf.fgene.2015.01.00011/full
work_keys_str_mv AT tamaraiglesiasalonso genotoxicevaluationofpolymericnanoparticles
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