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Functionalized Carbon Nanostructures Versus Drug Resistance: Promising Scenarios in Cancer Treatment.
- Source :
-
Molecules (Basel, Switzerland) [Molecules] 2020 Apr 30; Vol. 25 (9). Date of Electronic Publication: 2020 Apr 30. - Publication Year :
- 2020
-
Abstract
- Carbon nanostructures (CN) are emerging valuable materials for the assembly of highly engineered multifunctional nanovehicles for cancer therapy, in particular for counteracting the insurgence of multi-drug resistance (MDR). In this regard, carbon nanotubes (CNT), graphene oxide (GO), and fullerenes (F) have been proposed as promising materials due to their superior physical, chemical, and biological features. The possibility to easily modify their surface, conferring tailored properties, allows different CN derivatives to be synthesized. Although many studies have explored this topic, a comprehensive review evaluating the beneficial use of functionalized CNT vs G or F is still missing. Within this paper, the most relevant examples of CN-based nanosystems proposed for MDR reversal are reviewed, taking into consideration the functionalization routes, as well as the biological mechanisms involved and the possible toxicity concerns. The main aim is to understand which functional CN represents the most promising strategy to be further investigated for overcoming MDR in cancer.
- Subjects :
- ATP Binding Cassette Transporter, Subfamily B, Member 1 genetics
ATP Binding Cassette Transporter, Subfamily B, Member 1 metabolism
Animals
Antineoplastic Agents pharmacology
Antineoplastic Agents therapeutic use
Drug Carriers chemistry
Drug Delivery Systems
Drug Resistance, Multiple
Humans
Neoplasms drug therapy
Neoplasms genetics
Neoplasms metabolism
Neoplasms pathology
Antineoplastic Agents chemistry
Carbon chemistry
Drug Resistance, Neoplasm
Nanostructures chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1420-3049
- Volume :
- 25
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Molecules (Basel, Switzerland)
- Publication Type :
- Academic Journal
- Accession number :
- 32365886
- Full Text :
- https://doi.org/10.3390/molecules25092102