Dual-responsive controlled drug delivery based on ionically assembled nanoparticles

Ionically assembled nanoparticles (INPs) have been formed from poly(ionic liquid-co-N-isopropylacrylamide) with deoxycholic acid through electrostatic interaction. The structure and properties of the INPs were investigated by using (1)H NMR, Fourier transform infrared (FTIR), transmission electron m...

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Détails bibliographiques
Publié dans:Langmuir : the ACS journal of surfaces and colloids. - 1985. - 28(2012), 25 vom: 26. Juni, Seite 9413-20
Auteur principal: Cui, Wei (Auteur)
Autres auteurs: Lu, Xuemin, Cui, Kun, Niu, Lvye, Wei, Yen, Lu, Qinghua
Format: Article en ligne
Langue:English
Publié: 2012
Accès à la collection:Langmuir : the ACS journal of surfaces and colloids
Sujets:Journal Article Research Support, Non-U.S. Gov't Acrylamides Acrylic Resins Drug Carriers Ionic Liquids Polymers Protons Deoxycholic Acid 005990WHZZ plus... poly-N-isopropylacrylamide 25189-55-3 Doxorubicin 80168379AG
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520 |a Ionically assembled nanoparticles (INPs) have been formed from poly(ionic liquid-co-N-isopropylacrylamide) with deoxycholic acid through electrostatic interaction. The structure and properties of the INPs were investigated by using (1)H NMR, Fourier transform infrared (FTIR), transmission electron microscopy (TEM), dynamic light scattering (DLS), and so on. Due to pH-responsive deoxycholic acid (pK(a) = 6.2) and thermo responsive N-isopropylacrylamide included in the ionic complex, the INPs exhibit highly pH and thermal dual-responsive properties. The potential practical applications as drug delivery carriers were demonstrated using doxorubicin (DOX) as a model drug. With a lower pH (pH 5.2) and higher temperature (above 37 °C), structural collapse of the INPs occurred as well as release of DOX owing to protonated DA departure from the INPs and a lower LCST (lower critical solution temperature) at the pathological conditions. The result shows that 80% of DOX molecules were released from INPs within 48 h at pH 5.2, 43 °C, but only 30% of the drug was released within 48 h at 37 °C and pH 7.4. Moreover, drug-loaded INPs exhibit an inhibitory effect on cell growth 
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700 1 |a Niu, Lvye  |e verfasserin  |4 aut 
700 1 |a Wei, Yen  |e verfasserin  |4 aut 
700 1 |a Lu, Qinghua  |e verfasserin  |4 aut 
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