2020
DOI: 10.1016/j.ijpharm.2020.119244
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Design of surface ligands for blood compatible gold nanoparticles: Effect of charge and binding energy

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Cited by 24 publications
(13 citation statements)
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“…According to Ross and Subramanian [ 22 ], the positive values of the thermodynamic constants (ΔS and ΔH) for Fe 3 O 4 , Fe 3 O 4 @Ag, and Fe 3 O 4 @Ag/TCS NPs evidenced hydrophobic interactions with albumin [ 40 ]. The NP–protein association is frequently driven by weak interactions, and its mechanism enables the surface stabilization of each particle [ 41 ]. Hydrophobic interaction is the result of a partial withdrawal of the nonpolar group of water molecules and the solvation layer of the three NPs and/or albumin.…”
Section: Resultsmentioning
confidence: 99%
“…According to Ross and Subramanian [ 22 ], the positive values of the thermodynamic constants (ΔS and ΔH) for Fe 3 O 4 , Fe 3 O 4 @Ag, and Fe 3 O 4 @Ag/TCS NPs evidenced hydrophobic interactions with albumin [ 40 ]. The NP–protein association is frequently driven by weak interactions, and its mechanism enables the surface stabilization of each particle [ 41 ]. Hydrophobic interaction is the result of a partial withdrawal of the nonpolar group of water molecules and the solvation layer of the three NPs and/or albumin.…”
Section: Resultsmentioning
confidence: 99%
“…[2] Hemocompatibility can also be affected by the presence of BC, leading to a change in the interaction between nanostructures and blood components. [39,40] Blood interaction with BC-protein complexes can be made more complex by the interaction with anticoagulants. For example, it has been shown that the BC formed on the surface of poly(lactic acid) (PLA), polycaprolactone (PCL), silica, and a polystyrene vascular targeted carrier when exposed to both serum and whole blood is significantly affected by the presence of heparin, demonstrating an increase in their vascular targeting and adhesion efficiency.…”
Section: The Impact Of the Biomolecular Coronamentioning
confidence: 99%
“…In some studies, fluorescence quenching of both the endogenous fluorescence of proteins and fluorescently labeled proteins has been used to investigate the interaction between proteins and nanostructures. [24,40,133] One interesting example of fluorescently labeled protein use in BC studies is the work by Pinals et al, in which the exchange rate of two fluorescently labeled blood abundant proteins (namely, fibrinogen and albumin) on the surface of single-walled carbon nanotubes (SWCNTs) were investigated, functionalized with single-strand DNA (SSDNA) acting as a biosensor for dopamine. [133] The binding of both proteins and SSDNA fluorescently labeled on the surface of the SWCNT was monitored through the fluorescence quenching effect caused by the proximity of the fluorophore to the SWCNT surface.…”
Section: Indirect Techniques Based On Scattering Spectroscopy Colorim...mentioning
confidence: 99%
“…toxic cationic surfactant [84][85][86] and the conjugate systems of AuNWs-CTAB are proven to still contribute to toxicity to culture cells especially when the elevated concentrations of CTAB are present (50 g/ml commercial AuNWs-CTAB). With increasing the amount of AuNWs-CTAB solution, the cytotoxicity of the sample is increased caused by the nonspeci c binding tendency of CTAB to negatively charged cell surfaces by electrostatic interactions [87,88]. Once the interaction with the cell occurs, it forms blebs and holes on the cell and leading to cell death evident by the increase in the diameter of the ring zone.…”
Section: Cytotoxicity Evaluation Of As-synthesised and Commercial Aunwsmentioning
confidence: 99%