About the Influence of PEG Spacers on the Cytotoxicity of Titanate Nanotubes-Docetaxel Nanohybrids against a Prostate Cancer Cell Line

The association between chemotherapeutic drugs and metal oxide nanoparticles has sparked a rapidly growing interest in cancer nanomedicine. The elaboration of new engineered docetaxel (DTX)-nanocarriers based on titanate nanotubes (TiONts) was reported. The idea was to maintain the drug inside cance...

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Main Authors: Alexis Loiseau, Julien Boudon, Céline Mirjolet, Véronique Morgand, Nadine Millot
Format: Article
Language:English
Published: MDPI AG 2021-10-01
Series:Nanomaterials
Subjects:
Online Access:https://www.mdpi.com/2079-4991/11/10/2733
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author Alexis Loiseau
Julien Boudon
Céline Mirjolet
Véronique Morgand
Nadine Millot
author_facet Alexis Loiseau
Julien Boudon
Céline Mirjolet
Véronique Morgand
Nadine Millot
author_sort Alexis Loiseau
collection DOAJ
description The association between chemotherapeutic drugs and metal oxide nanoparticles has sparked a rapidly growing interest in cancer nanomedicine. The elaboration of new engineered docetaxel (DTX)-nanocarriers based on titanate nanotubes (TiONts) was reported. The idea was to maintain the drug inside cancer cells and avoid multidrug resistance mechanisms, which often limit drug efficacy by decreasing their intracellular concentrations in tumor cells. HS-PEG<sub>n</sub>-COOH (PEG: polyethylene glycol, n = 3000, 5000, 10,000) was conjugated, in an organic medium by covalent linkages, on TiONts surface. This study aimed to investigate the influence of different PEG derivatives chain lengths on the TiONts colloidal stability, on the PEG<sub>n</sub> density and conformation, as well as on the DTX biological activity in a prostate cancer model (human PC-3 prostate adenocarcinoma cells). In vitro tests highlighted significant cytotoxicities of the drug after loading DTX on PEG<sub>n</sub>-modified TiONts (TiONts-PEG<sub>n</sub>-DTX). Higher grafting densities for shorter PEGylated chains were most favorable on DTX cytotoxicity by promoting both colloidal stability in biological media and cells internalization. This promising strategy involves a better understanding of nanohybrid engineering, particularly on the PEGylated chain length influence, and can thus become a potent tool in nanomedicine to fight against cancer.
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spelling doaj.art-9565dcd809224a2c9291c858a71f6f632023-11-22T19:25:48ZengMDPI AGNanomaterials2079-49912021-10-011110273310.3390/nano11102733About the Influence of PEG Spacers on the Cytotoxicity of Titanate Nanotubes-Docetaxel Nanohybrids against a Prostate Cancer Cell LineAlexis Loiseau0Julien Boudon1Céline Mirjolet2Véronique Morgand3Nadine Millot4Laboratoire Interdisciplinaire Carnot de Bourgogne, UMR 6303 CNRS Université Bourgogne Franche-Comté, BP 47870, CEDEX, 21078 Dijon, FranceLaboratoire Interdisciplinaire Carnot de Bourgogne, UMR 6303 CNRS Université Bourgogne Franche-Comté, BP 47870, CEDEX, 21078 Dijon, FranceINSERM 1231, Cadir Team, CEDEX, 21078 Dijon, FranceRadiotherapy Department, Georges-Francois Leclerc Cancer Center, CEDEX, 21079 Dijon, FranceLaboratoire Interdisciplinaire Carnot de Bourgogne, UMR 6303 CNRS Université Bourgogne Franche-Comté, BP 47870, CEDEX, 21078 Dijon, FranceThe association between chemotherapeutic drugs and metal oxide nanoparticles has sparked a rapidly growing interest in cancer nanomedicine. The elaboration of new engineered docetaxel (DTX)-nanocarriers based on titanate nanotubes (TiONts) was reported. The idea was to maintain the drug inside cancer cells and avoid multidrug resistance mechanisms, which often limit drug efficacy by decreasing their intracellular concentrations in tumor cells. HS-PEG<sub>n</sub>-COOH (PEG: polyethylene glycol, n = 3000, 5000, 10,000) was conjugated, in an organic medium by covalent linkages, on TiONts surface. This study aimed to investigate the influence of different PEG derivatives chain lengths on the TiONts colloidal stability, on the PEG<sub>n</sub> density and conformation, as well as on the DTX biological activity in a prostate cancer model (human PC-3 prostate adenocarcinoma cells). In vitro tests highlighted significant cytotoxicities of the drug after loading DTX on PEG<sub>n</sub>-modified TiONts (TiONts-PEG<sub>n</sub>-DTX). Higher grafting densities for shorter PEGylated chains were most favorable on DTX cytotoxicity by promoting both colloidal stability in biological media and cells internalization. This promising strategy involves a better understanding of nanohybrid engineering, particularly on the PEGylated chain length influence, and can thus become a potent tool in nanomedicine to fight against cancer.https://www.mdpi.com/2079-4991/11/10/2733titanate nanotubespolyethylene glycolcolloidal stabilitydocetaxelcytotoxicityprostate cancer cells
spellingShingle Alexis Loiseau
Julien Boudon
Céline Mirjolet
Véronique Morgand
Nadine Millot
About the Influence of PEG Spacers on the Cytotoxicity of Titanate Nanotubes-Docetaxel Nanohybrids against a Prostate Cancer Cell Line
Nanomaterials
titanate nanotubes
polyethylene glycol
colloidal stability
docetaxel
cytotoxicity
prostate cancer cells
title About the Influence of PEG Spacers on the Cytotoxicity of Titanate Nanotubes-Docetaxel Nanohybrids against a Prostate Cancer Cell Line
title_full About the Influence of PEG Spacers on the Cytotoxicity of Titanate Nanotubes-Docetaxel Nanohybrids against a Prostate Cancer Cell Line
title_fullStr About the Influence of PEG Spacers on the Cytotoxicity of Titanate Nanotubes-Docetaxel Nanohybrids against a Prostate Cancer Cell Line
title_full_unstemmed About the Influence of PEG Spacers on the Cytotoxicity of Titanate Nanotubes-Docetaxel Nanohybrids against a Prostate Cancer Cell Line
title_short About the Influence of PEG Spacers on the Cytotoxicity of Titanate Nanotubes-Docetaxel Nanohybrids against a Prostate Cancer Cell Line
title_sort about the influence of peg spacers on the cytotoxicity of titanate nanotubes docetaxel nanohybrids against a prostate cancer cell line
topic titanate nanotubes
polyethylene glycol
colloidal stability
docetaxel
cytotoxicity
prostate cancer cells
url https://www.mdpi.com/2079-4991/11/10/2733
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