Surface modification of magnetic nanoparticles (MNPs) has been reported to play a significant role in determining their interactions with cell membranes. In this research, the interactions between polymer functionalized (chitosan, CHI or diethylamino-ethyl dextran, DEAE-D) FeO MNPs, pharmaceutical drugs and model cell membranes were investigated by Langmuir isotherms and adsorption measurements. In this study, 1,2-distearoyl-sn-glycerol-3-phosphate (DSPA) phospholipid monolayers were used as cell membrane models. Insertion experiments demonstrate that diclofenac (DCFN) is not absorbed at the air-water interface, whereas triflupromazine (TFPZ) has a MIP (maximum insertion pressure) of 35 m Nm. The insertion of composites MNPs:TFPZ or DCFN has larger MIP values, indicating that the MNPs are adsorbed on the monolayer with the drugs. An FeO@CHI:DCFN composite presented an MIP of 39 m Nm and FeO@DEAE-D:DCFN presented an impressive MIP of 67 mNm. In the case of TFPZ, the enhancement in the MIP values is also evident, being 42 mNm for FeO@CHI:TFPZ and 40 mNm for FeO@DEAE-D:DCFN composite. All MNPs:drugs composites have MIP values greater than commonly accepted membrane pressure values, indicating that MNPs:drugs can penetrate a cellular membrane. The fact that the composite MNPs:drugs present greater MIP values than separated compounds indicates that polymer-coated MNPs can act as good drug delivery systems.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9961141 | PMC |
| http://dx.doi.org/10.3390/pharmaceutics15020311 | DOI Listing |
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