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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.
Impact Factor
Scopus SNIP
Web of Science
Times Cited
Times Cited
Scopus
Cited By
Cited By
Altmetric
12.124
2.240
46
60
Anmerkungen
Besondere Publikation
Auf Hompepage verbergern
Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Schlagwörter
Colloidal Stability ; Gold Nanoparticles ; Protein Coronas ; Surface Chemistry Dependence; Adsorption; Cells; Electrophoresis; Polymer; Target; Size; Peg
Sprache
englisch
Veröffentlichungsjahr
2017
HGF-Berichtsjahr
2017
ISSN (print) / ISBN
1616-301X
e-ISSN
1616-3028
Zeitschrift
Advanced functional materials
Quellenangaben
Band: 27,
Heft: 42,
Artikelnummer: 1701956
Verlag
Wiley
Verlagsort
Weinheim
Begutachtungsstatus
Peer reviewed
Institut(e)
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
Forschungsfeld(er)
Genetics and Epidemiology
Enabling and Novel Technologies
Lung Research
Radiation Sciences
Enabling and Novel Technologies
Lung Research
Radiation Sciences
PSP-Element(e)
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