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...
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doaj-b1cbc4594fca4b148eb9aa910d01e7662020-11-25T00:56:45ZengMDPI AGPharmaceutics1999-49232018-07-011039110.3390/pharmaceutics10030091pharmaceutics10030091Gold Nanoparticles for Targeting Varlitinib to Human Pancreatic Cancer CellsSílvia Castro Coelho0Daniel Pires Reis1Maria Carmo Pereira2Manuel A. N. Coelho3LEPABE—Laboratory for Process Engineering, Environment, Biotechnology and Energy, Faculty of Engineering, University of Porto, Rua Dr Roberto Frias, 4200-465 Porto, PortugalLEPABE—Laboratory for Process Engineering, Environment, Biotechnology and Energy, Faculty of Engineering, University of Porto, Rua Dr Roberto Frias, 4200-465 Porto, PortugalLEPABE—Laboratory for Process Engineering, Environment, Biotechnology and Energy, Faculty of Engineering, University of Porto, Rua Dr Roberto Frias, 4200-465 Porto, PortugalLEPABE—Laboratory for Process Engineering, Environment, Biotechnology and Energy, Faculty of Engineering, University of Porto, Rua Dr Roberto Frias, 4200-465 Porto, PortugalColloidal 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.http://www.mdpi.com/1999-4923/10/3/91gold nanoparticlestyrosine conjugationpancreatic cells |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Sílvia Castro Coelho Daniel Pires Reis Maria Carmo Pereira Manuel A. N. Coelho |
spellingShingle |
Sílvia Castro Coelho Daniel Pires Reis Maria Carmo Pereira Manuel A. N. Coelho Gold Nanoparticles for Targeting Varlitinib to Human Pancreatic Cancer Cells Pharmaceutics gold nanoparticles tyrosine conjugation pancreatic cells |
author_facet |
Sílvia Castro Coelho Daniel Pires Reis Maria Carmo Pereira Manuel A. N. Coelho |
author_sort |
Sílvia Castro Coelho |
title |
Gold Nanoparticles for Targeting Varlitinib to Human Pancreatic Cancer Cells |
title_short |
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_sort |
gold nanoparticles for targeting varlitinib to human pancreatic cancer cells |
publisher |
MDPI AG |
series |
Pharmaceutics |
issn |
1999-4923 |
publishDate |
2018-07-01 |
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. |
topic |
gold nanoparticles tyrosine conjugation pancreatic cells |
url |
http://www.mdpi.com/1999-4923/10/3/91 |
work_keys_str_mv |
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