Poly(ethylene glycol) based nanotubes for tuneable drug delivery to glioblastoma multiforme.


Journal

Nanoscale advances
ISSN: 2516-0230
Titre abrégé: Nanoscale Adv
Pays: England
ID NLM: 101738708

Informations de publication

Date de publication:
13 Oct 2020
Historique:
received: 10 06 2020
accepted: 20 08 2020
entrez: 22 9 2022
pubmed: 24 8 2020
medline: 24 8 2020
Statut: epublish

Résumé

Glioblastoma multiforme (GBM) is the most aggressive type of malignant brain tumour, which is associated with a poor two-year survival rate and a high rate of fatal recurrence near the original tumour. Focal/local drug delivery devices hold promise for improving therapeutic outcomes for GBM by increasing drug concentrations locally at the tumour site, or by facilitating the use of potent anti-cancer drugs that are poorly permeable across the blood brain barrier (BBB). For inoperable tumours, stereotactic delivery to the tumour necessitates the development of nanoscale/microscale injectable drug delivery devices. Herein we assess the ability of a novel class of polymer nanotube (based on poly(ethylene glycol) (PEG)) to load doxorubicin (a mainstay breast cancer therapeutic with poor BBB permeability) and release it slowly. The drug loading properties of the PEG nanotubes could be tuned by varying the degree of carboxylic acid functionalisation and hence the capacity of the nanotubes to electrostatically bind and load doxorubicin. 70% of the drug was released over the first seven days followed by sustained drug release for the remaining two weeks tested. Unloaded PEG nanotubes showed no toxicity to any of the cell types analysed, whereas doxorubicin loaded nanotubes decreased GBM cell viability (C6, U-87 and U-251) in a dose dependent manner in 2D

Identifiants

pubmed: 36132909
doi: 10.1039/d0na00471e
pii: d0na00471e
pmc: PMC9418774
doi:

Types de publication

Journal Article

Langues

eng

Pagination

4498-4509

Informations de copyright

This journal is © The Royal Society of Chemistry.

Déclaration de conflit d'intérêts

There are no conflicts to declare.

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Auteurs

Majed Alghamdi (M)

School of Pharmacy and Pharmaceutical Sciences, Cardiff University King Edward VII Avenue Cardiff CF10 3NB UK newlandb@cardiff.ac.uk.
School of Pharmacy, King Abdulaziz University Jeddah 21589 Saudi Arabia.

Filippo Chierchini (F)

School of Pharmacy and Pharmaceutical Sciences, Cardiff University King Edward VII Avenue Cardiff CF10 3NB UK newlandb@cardiff.ac.uk.

Dimitri Eigel (D)

Leibniz-Institut für Polymerforschung Dresden, Max Bergmann Center of Biomaterials Dresden Hohe Straße 6 D-01069 Dresden Germany.

Christian Taplan (C)

Leibniz-Institut für Polymerforschung Dresden, Max Bergmann Center of Biomaterials Dresden Hohe Straße 6 D-01069 Dresden Germany.

Thomas Miles (T)

School of Pharmacy and Pharmaceutical Sciences, Cardiff University King Edward VII Avenue Cardiff CF10 3NB UK newlandb@cardiff.ac.uk.

Dagmar Pette (D)

Leibniz-Institut für Polymerforschung Dresden, Max Bergmann Center of Biomaterials Dresden Hohe Straße 6 D-01069 Dresden Germany.

Petra B Welzel (PB)

Leibniz-Institut für Polymerforschung Dresden, Max Bergmann Center of Biomaterials Dresden Hohe Straße 6 D-01069 Dresden Germany.

Carsten Werner (C)

Leibniz-Institut für Polymerforschung Dresden, Max Bergmann Center of Biomaterials Dresden Hohe Straße 6 D-01069 Dresden Germany.

Wenxin Wang (W)

Charles Institute of Dermatology, School of Medicine, University College Dublin Ireland.

Catia Neto (C)

School of Pharmacy and Pharmaceutical Sciences, Cardiff University King Edward VII Avenue Cardiff CF10 3NB UK newlandb@cardiff.ac.uk.

Mark Gumbleton (M)

School of Pharmacy and Pharmaceutical Sciences, Cardiff University King Edward VII Avenue Cardiff CF10 3NB UK newlandb@cardiff.ac.uk.

Ben Newland (B)

School of Pharmacy and Pharmaceutical Sciences, Cardiff University King Edward VII Avenue Cardiff CF10 3NB UK newlandb@cardiff.ac.uk.
Leibniz-Institut für Polymerforschung Dresden, Max Bergmann Center of Biomaterials Dresden Hohe Straße 6 D-01069 Dresden Germany.

Classifications MeSH