Magnetoliposomes Containing Multicore Nanoparticles and a New Antitumor Thienopyridine Compound with Potential Application in Chemo/Thermotherapy.
Fábio A C LopesAndré V F FernandesJuliana M RodriguesMaria João R P QueirozBernardo G AlmeidaAna PiresAndré M PereiraJoão Pedro AraújoElisabete M S CastanheiraAna Rita O RodriguesPaulo J G CoutinhoPublished in: Biomedicines (2022)
Multicore magnetic nanoparticles of manganese ferrite were prepared using carboxymethyl dextran as an agglutinating compound or by an innovative method using melamine as a cross-coupling agent. The nanoparticles prepared using melamine exhibited a flower-shape structure, a saturation magnetization of 6.16 emu/g and good capabilities for magnetic hyperthermia, with a specific absorption rate (SAR) of 0.14 W/g. Magnetoliposome-like structures containing the multicore nanoparticles were prepared, and their bilayer structure was confirmed by FRET (Förster Resonance Energy Transfer) assays. The nanosystems exhibited sizes in the range of 250-400 nm and a low polydispersity index. A new antitumor thienopyridine derivative, 7-[4-(pyridin-2-yl)-1 H -1,2,3-triazol-1-yl]thieno[3,2- b ]pyridine, active against HeLa (cervical carcinoma), MCF-7 (breast adenocarcinoma), NCI-H460 (non-small-cell lung carcinoma) and HepG2 (hepatocellular carcinoma) cell lines, was loaded in these nanocarriers, obtaining a high encapsulation efficiency of 98 ± 2.6%. The results indicate that the new magnetoliposomes can be suitable for dual cancer therapy (combined magnetic hyperthermia and chemotherapy).
Keyphrases
- energy transfer
- cancer therapy
- molecularly imprinted
- drug delivery
- quantum dots
- magnetic nanoparticles
- locally advanced
- photodynamic therapy
- single cell
- squamous cell carcinoma
- high throughput
- walled carbon nanotubes
- high resolution
- breast cancer cells
- stem cells
- rectal cancer
- cell therapy
- drug release
- cell death
- combination therapy
- climate change
- cell proliferation
- water soluble
- simultaneous determination