2019
Lipidic Liquid Crystalline Cubic Phases and Magnetocubosomes as Methotrexate Carriers
MIERZWA, Monika, Adrianna CYTRYNIAK, Pawel KRYSINSKI a Renata BILEWICZZákladní údaje
Originální název
Lipidic Liquid Crystalline Cubic Phases and Magnetocubosomes as Methotrexate Carriers
Autoři
MIERZWA, Monika, Adrianna CYTRYNIAK, Pawel KRYSINSKI a Renata BILEWICZ
Vydání
Nanomaterials, BASEL, MDPI, 2019, 2079-4991
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
21000 2.10 Nano-technology
Stát vydavatele
Švýcarsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 4.324
Organizační jednotka
CIISB II
UT WoS
000467768800152
Klíčová slova anglicky
methotrexate; cubic phase; magnetocubosomes; monoolein; liquid crystalline phase; drug delivery system; alternating magnetic field
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 11. 6. 2024 09:28, Mgr. Eva Dubská
Anotace
V originále
The release profiles of methotrexate, an anticancer drug, from the monoolein liquid crystalline cubic phases were studied. The cubic phases were used either in the form of a lipidic film deposited onto a glassy carbon electrode surface or in the dispersed form of magnetocubosomes, which are considered a prospective hybrid drug delivery system. Commonly, cubosomes or liposomes are employed, but not in the case of toxic methotrexate, known to block the receptors responsible for folate transport into the cells. The release profiles of the drug from the lipidic films were monitored electrochemically and described using the Higuchi model. They were also modified via changes in temperature; the release was faster, although it deviated from the model when the temperature was increased. Cubic phase nanoparticles (magnetocubosomes) containing hydrophobic magnetic nanoparticles placed in an alternating magnetic field of low frequency and amplitude, stimulated drug release from the suspension, which was monitored spectroscopically. These new biocompatible hybrid nanomaterials in the dispersed form allow to control the release of the drug at the appropriate sites, can be easily separated or relocated under external magnetic field and await further investigations of their in vitro cytotoxicity and in vivo biodistribution.
Návaznosti
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