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• W2078333582 abstract "Ingested, inhaled or injected particles come into contact with biological fluids containing polymers, such as the protein fibrinogen. We studied interactions between well-characterized submicron particles or nanoparticles (NPs) and human fibrinogen. In vitro aggregation and zeta potential measurements of different sized and functionalized polystyrene, carbon black and silica NPs suspended in fibrinogen solutions were made. Particle size, surface charge and aggregation behaviour significantly changed in the presence of fibrinogen. Polymer (protein) bridging and bridge flocculation was observed. We concluded: (1) NP aggregation rate in a fibrinogen solution depended on particle surface type; (2) amine-functionalized particles aggregated more slowly in fibrinogen; and (3) particle morphology strongly influenced biologically available surface for protein attachment, but this did not correlate well with particle surface area for complex particles (calculated or measured). Interaction of particles and NPs with pro-coagulant polymers may therefore dictate the NP surface dose presentation to cells/organs and subsequent cellular effects, in and ex vivo." @default.
• W2078333582 created "2016-06-24" @default.
• W2078333582 creator A5012920366 @default.
• W2078333582 creator A5037340706 @default.
• W2078333582 creator A5068968591 @default.
• W2078333582 date "2010-06-14" @default.
• W2078333582 modified "2023-09-23" @default.
• W2078333582 title "Particle and nanoparticle interactions with fibrinogen: the importance of aggregation in nanotoxicology" @default.
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• W2078333582 doi "https://doi.org/10.3109/17435390.2010.489724" @default.
• W2078333582 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/21417688" @default.
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