TY - JOUR
T1 - Opposite effects produced by magnetic nanoparticles:Phospholipid films generated at a liquid/liquid interface, in the drug transfer processes
AU - Betancourt, Sara N.Moya
AU - Riva, Julieta S.
N1 - Publisher Copyright:
© 2023 Elsevier Ltd
PY - 2023/3/1
Y1 - 2023/3/1
N2 - The interaction between Fe3O4 magnetic nanoparticles (MNPs) coated with polysaccharides, and different phospholipids adsorbed at a water|1,2-dichloroethane interface, was studied employing cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and capacity curves. For this study, an anionic phospholipid, distearoyl phosphatidic acid (DSPA), and a zwitterionic phospholipid distearoyl phosphatidylethanolamine (DSPE) were used, which have the same carbonated chain. Fe3O4 nanoparticles were coated with two different polysaccharides, one lineal, chitosan (CHI), and other with a branched structure, diethylaminoethyl dextran (DEAE-D), both commonly used in medical applications. The effect of the MNPs coating agents in the final interaction with MNPs:phospholipid hybrid films was evaluated. EIS confirm that the presence of Fe3O4@CHI:DSPA mixture film conduces to a homogeneous film at the interface, in contrast, for Fe3O4@DEAE-D:DSPA mixture films, conduces to a inhomogeneous film with pores formation. In addition, the effect of this hybrid films (MNPs:phospholipid) in the anionic diclofenac (DCFNC−) and cationic triflupromazine (HTFPZ+) transfer process across the water|1,2-dichloroethane interface was studied. It was demonstrated that Fe3O4@CHI:DSPA film can totally block DCFNC− transfer process but for Fe3O4@DEAE-D:DSPA or DSPE film the DCFNC− can transfer across the uncovered zones present at the interface. Otherwise, for positively charged HTFPZ+, the drug transfer is higher in presence of MNPs:phospholipid mixture film due to a sum of effects, electrostatic interaction between HTFPZ+ and phospholipid and hydrophobic interactions between HTFPZ+ and polysaccharide coated MNPs.
AB - The interaction between Fe3O4 magnetic nanoparticles (MNPs) coated with polysaccharides, and different phospholipids adsorbed at a water|1,2-dichloroethane interface, was studied employing cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and capacity curves. For this study, an anionic phospholipid, distearoyl phosphatidic acid (DSPA), and a zwitterionic phospholipid distearoyl phosphatidylethanolamine (DSPE) were used, which have the same carbonated chain. Fe3O4 nanoparticles were coated with two different polysaccharides, one lineal, chitosan (CHI), and other with a branched structure, diethylaminoethyl dextran (DEAE-D), both commonly used in medical applications. The effect of the MNPs coating agents in the final interaction with MNPs:phospholipid hybrid films was evaluated. EIS confirm that the presence of Fe3O4@CHI:DSPA mixture film conduces to a homogeneous film at the interface, in contrast, for Fe3O4@DEAE-D:DSPA mixture films, conduces to a inhomogeneous film with pores formation. In addition, the effect of this hybrid films (MNPs:phospholipid) in the anionic diclofenac (DCFNC−) and cationic triflupromazine (HTFPZ+) transfer process across the water|1,2-dichloroethane interface was studied. It was demonstrated that Fe3O4@CHI:DSPA film can totally block DCFNC− transfer process but for Fe3O4@DEAE-D:DSPA or DSPE film the DCFNC− can transfer across the uncovered zones present at the interface. Otherwise, for positively charged HTFPZ+, the drug transfer is higher in presence of MNPs:phospholipid mixture film due to a sum of effects, electrostatic interaction between HTFPZ+ and phospholipid and hydrophobic interactions between HTFPZ+ and polysaccharide coated MNPs.
KW - Chitosan
KW - DEAE-dextran, Diclofenac, Triflupromazine, Distearoyl phosphatidic acid, Distearoyl phosphatidylethanolamine
KW - Liquid|liquid interfaces
KW - Magnetite
UR - https://www.scopus.com/pages/publications/85147544213
U2 - 10.1016/j.electacta.2023.141967
DO - 10.1016/j.electacta.2023.141967
M3 - Article
AN - SCOPUS:85147544213
SN - 0013-4686
VL - 443
JO - Electrochimica Acta
JF - Electrochimica Acta
M1 - 141967
ER -