2020
DOI: 10.1007/s10853-020-04784-3
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Poly (ε-caprolactone)/poly (N-vinyl-2-pyrrolidone) core–shell nanofibers loaded by multi-walled carbon nanotubes and 5-fluorouracil: an anticancer drug delivery system

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Cited by 35 publications
(14 citation statements)
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“…Moreover, the incorporation of a drug onto the core, which in turn will be coated by the shell, could effectively control the drug's release profile and protect the drug from damage, offering a great advantage to this type of structure. [55,126,127]…”
Section: Coaxial Electrospinningmentioning
confidence: 99%
“…Moreover, the incorporation of a drug onto the core, which in turn will be coated by the shell, could effectively control the drug's release profile and protect the drug from damage, offering a great advantage to this type of structure. [55,126,127]…”
Section: Coaxial Electrospinningmentioning
confidence: 99%
“…Localized micelle release was complemented by targeting ligands which promoted micelle endocytosis [ 127 ]. The addition of nanostructures was also used to improve tensile and drug releasing properties of PVP-based NFs [ 128 ]. While PVP core was used to encapsulate unstable 5-fluorouracil (5FU), the addition of PCL and multi-walled carbon nanotubes (MWCNT) to the PVP shell resulted in improved sustainable drug release and mechanical properties.…”
Section: Therapeutic Applicationsmentioning
confidence: 99%
“…MWCNTs conjugated with PEI, an antiviral drug ribavirin ( Figure 4 ) and the pearl gentian grouper nervous necrosis virus (PGNNV)-specific nanobody showed an increasing distribution in PGNNV-infected cells, powerful anti-PGNNV ability both in vitro and in vivo and such formulations can be an effective tool for virus-induced central nervous system disease targeted therapy [ 285 ]. PCL/poly( N -vinyl-2-pyrrolidone) (PVP) core-shell nanofibers showing mean diameter 300–400 nm and containing MWCNTs and 5-FU loaded in the core of these nanofibers showed sustained and prolonged drug release (up to 85% after 528 h) and cytotoxicity against HeLa cells (50.35% after 72 h), suggesting that this drug delivery system can be applied in post-surgical delivery of anticancer drugs [ 286 ].…”
Section: Carbon Nanotubesmentioning
confidence: 99%