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Colloidal stability and surface chemistry are key factors for the composition of the protein corona of inorganic gold nanoparticles.
Adv. Func. Mat. 27:1701956 (2017)
To study the influence of colloidal stability on protein corona formation, gold nanoparticles are synthesized with five distinct surface modifications: coating with citric acid, bis(p-sulfonatophenyl)phenylphosphine dihydrate dipotassium salt, thiol-terminated methoxy-polyethylene glycol, dodecylamine-grafted poly(isobutylene-alt-maleic anhydride), and dodecylamine-grafted poly(isobutylene-alt-maleic anhydride) conjugated with polyethylene glycol. The nanoparticles are incubated with serum or bronchoalveolar lavage fluid from C57BL/6 mice (15 min or 24 h) to assess the effect of differential nanoparticle surface presentation on protein corona formation in the air–blood barrier exposure pathway. Proteomic quantification and nanoparticle size measurements are used to assess protein corona formation. We show that surface modification has a clear effect on the size and the composition of the protein corona that is related to the colloidal stability of the studied nanoparticles. Additionally, differences in the composition and size of the protein corona are shown between biological media and duration of exposure, indicating evolution of the corona through this exposure pathway. Consequently, a major determinant of protein corona formation is the colloidal stability of nanoparticles in biological media and chemical or environmental modification of the nanoparticles alters the surface presentation of the functional epitope in vivo. Therefore, the colloidal stability of nanoparticles has a decisive influence on nano–bio interactions.
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Publication type
Article: Journal article
Document type
Scientific Article
Keywords
Colloidal Stability ; Gold Nanoparticles ; Protein Coronas ; Surface Chemistry Dependence; Adsorption; Cells; Electrophoresis; Polymer; Target; Size; Peg
Language
english
Publication Year
2017
HGF-reported in Year
2017
ISSN (print) / ISBN
1616-301X
e-ISSN
1616-3028
Journal
Advanced functional materials
Quellenangaben
Volume: 27,
Issue: 42,
Article Number: 1701956
Publisher
Wiley
Publishing Place
Weinheim
Reviewing status
Peer reviewed
Institute(s)
Institute of Epidemiology (EPI)
CF Metabolomics & Proteomics (CF-MPC)
Institute of Lung Health and Immunity (LHI)
Institute of Radiation Protection (ISS)
CF Metabolomics & Proteomics (CF-MPC)
Institute of Lung Health and Immunity (LHI)
Institute of Radiation Protection (ISS)
POF-Topic(s)
30202 - Environmental Health
30203 - Molecular Targets and Therapies
30504 - Mechanisms of Genetic and Environmental Influences on Health and Disease
30203 - Molecular Targets and Therapies
30504 - Mechanisms of Genetic and Environmental Influences on Health and Disease
Research field(s)
Genetics and Epidemiology
Enabling and Novel Technologies
Lung Research
Radiation Sciences
Enabling and Novel Technologies
Lung Research
Radiation Sciences
PSP Element(s)
G-504000-001
G-505700-001
G-505000-001
G-501100-006
G-505700-001
G-505000-001
G-501100-006
WOS ID
WOS:000414719300020
Scopus ID
85030317404
Erfassungsdatum
2017-10-05