ZrO sub(2) nanoparticles labeled viaa native protein corona: detection by fluorescence microscopy and Raman microspectroscopy in rat lungs
ZrO sub(2) nanoparticles are frequently used in composite materials such as dental fillers from where they may be released and inhaled upon polishing and grinding. Since the overall distribution of ZrO sub(2) NP inside the lung parenchyma can hardly be observed by routine histology, here a labeling...
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Veröffentlicht in: | Analyst (London) 2015-07, Vol.140 (15), p.5120-5128 |
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creator | Silge, Anja Braeutigam, Katharina Bocklitz, Thomas Rosch, Petra Vennemann, Antje Schmitz, Inge Popp, Juergen Wiemann, Martin |
description | ZrO sub(2) nanoparticles are frequently used in composite materials such as dental fillers from where they may be released and inhaled upon polishing and grinding. Since the overall distribution of ZrO sub(2) NP inside the lung parenchyma can hardly be observed by routine histology, here a labeling with a fluorphore was used secondary to the adsorption of serum proteins. Particles were then intratracheally instilled into rat lungs. After 3 h fluorescent structures consisted of agglomerates scattered throughout the lung parenchyma, which were mainly concentrated in alveolar macrophages after 3 d. A detection method based on Raman microspectroscopy was established to investigate the chemical composition of those fluorescent structures in detail. Raman measurements were arranged such that no spectral interference with the protein-bound fluorescence label was evident. Applying chemometrical methods, Raman signals of the ZrO sub(2) nanomaterial were co-localized with the fluorescence label, indicating the stability of the nanomaterial-protein-dye complex inside the rat lung. The combination of Raman microspectroscopy and adsorptive fluorescence labeling may, therefore, become a useful tool for studying the localization of protein-coated nanomaterials in cells and tissues. |
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Since the overall distribution of ZrO sub(2) NP inside the lung parenchyma can hardly be observed by routine histology, here a labeling with a fluorphore was used secondary to the adsorption of serum proteins. Particles were then intratracheally instilled into rat lungs. After 3 h fluorescent structures consisted of agglomerates scattered throughout the lung parenchyma, which were mainly concentrated in alveolar macrophages after 3 d. A detection method based on Raman microspectroscopy was established to investigate the chemical composition of those fluorescent structures in detail. Raman measurements were arranged such that no spectral interference with the protein-bound fluorescence label was evident. Applying chemometrical methods, Raman signals of the ZrO sub(2) nanomaterial were co-localized with the fluorescence label, indicating the stability of the nanomaterial-protein-dye complex inside the rat lung. 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source | Royal Society Of Chemistry Journals; Royal Society of Chemistry Journals Archive; Alma/SFX Local Collection |
subjects | Concentration (composition) Fluorescence Labels Lungs Marking Nanoparticles Nanostructure Zirconium dioxide |
title | ZrO sub(2) nanoparticles labeled viaa native protein corona: detection by fluorescence microscopy and Raman microspectroscopy in rat lungs |
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