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Gold Nanoparticles for Targeting Varlitinib to Human Pancreatic Cancer Cells
Colloidal gold nanoparticles are targeting probes to improve varlitinib delivery into cancer cells. The nanoconjugates were designed by the bioconjugation of pegylated gold nanoparticles with varlitinib via carbodiimide-mediated cross-linking and characterized by infrared and X-ray photoelectron spe...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6161021/ https://www.ncbi.nlm.nih.gov/pubmed/30002279 http://dx.doi.org/10.3390/pharmaceutics10030091 |
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author | Coelho, Sílvia Castro Reis, Daniel Pires Pereira, Maria Carmo Coelho, Manuel A. N. |
author_facet | Coelho, Sílvia Castro Reis, Daniel Pires Pereira, Maria Carmo Coelho, Manuel A. N. |
author_sort | Coelho, Sílvia Castro |
collection | PubMed |
description | Colloidal gold nanoparticles are targeting probes to improve varlitinib delivery into cancer cells. The nanoconjugates were designed by the bioconjugation of pegylated gold nanoparticles with varlitinib via carbodiimide-mediated cross-linking and characterized by infrared and X-ray photoelectron spectroscopy. The drug release response shows an initial delay and a complete drug release after 72 h is detected. In vitro experiments with MIA PaCa-2 cells corroborate that PEGAuNPsVarl conjugates increase the varlitinib toxic effect at very low concentrations (IC50 = 80 nM) if compared with varlitinib alone (IC50 = 259 nM). Our results acknowledge a decrease of drug side effects in normal cells and an enhancement of drug efficacy against to the pancreatic cancer cells reported. |
format | Online Article Text |
id | pubmed-6161021 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61610212018-10-01 Gold Nanoparticles for Targeting Varlitinib to Human Pancreatic Cancer Cells Coelho, Sílvia Castro Reis, Daniel Pires Pereira, Maria Carmo Coelho, Manuel A. N. Pharmaceutics Article Colloidal gold nanoparticles are targeting probes to improve varlitinib delivery into cancer cells. The nanoconjugates were designed by the bioconjugation of pegylated gold nanoparticles with varlitinib via carbodiimide-mediated cross-linking and characterized by infrared and X-ray photoelectron spectroscopy. The drug release response shows an initial delay and a complete drug release after 72 h is detected. In vitro experiments with MIA PaCa-2 cells corroborate that PEGAuNPsVarl conjugates increase the varlitinib toxic effect at very low concentrations (IC50 = 80 nM) if compared with varlitinib alone (IC50 = 259 nM). Our results acknowledge a decrease of drug side effects in normal cells and an enhancement of drug efficacy against to the pancreatic cancer cells reported. MDPI 2018-07-12 /pmc/articles/PMC6161021/ /pubmed/30002279 http://dx.doi.org/10.3390/pharmaceutics10030091 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Coelho, Sílvia Castro Reis, Daniel Pires Pereira, Maria Carmo Coelho, Manuel A. N. Gold Nanoparticles for Targeting Varlitinib to Human Pancreatic Cancer Cells |
title | Gold Nanoparticles for Targeting Varlitinib to Human Pancreatic Cancer Cells |
title_full | Gold Nanoparticles for Targeting Varlitinib to Human Pancreatic Cancer Cells |
title_fullStr | Gold Nanoparticles for Targeting Varlitinib to Human Pancreatic Cancer Cells |
title_full_unstemmed | Gold Nanoparticles for Targeting Varlitinib to Human Pancreatic Cancer Cells |
title_short | Gold Nanoparticles for Targeting Varlitinib to Human Pancreatic Cancer Cells |
title_sort | gold nanoparticles for targeting varlitinib to human pancreatic cancer cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6161021/ https://www.ncbi.nlm.nih.gov/pubmed/30002279 http://dx.doi.org/10.3390/pharmaceutics10030091 |
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