2 research outputs found
Fluorescent Nanowire Heterostructures as a Versatile Tool for Biology Applications
Nanowires are increasingly used in
biology, as sensors, as injection
devices, and as model systems for toxicity studies. Currently, in
situ visualization of nanowires in biological media is done using
organic dyes, which are prone to photobleaching, or using microscopy
methods which either yield poor resolution or require a sophisticated
setup. Here we show that inherently fluorescent nanowire axial heterostructures
can be used to localize and identify nanowires in cells and tissue.
By synthesizing GaP–GaInP nanowire heterostructures, with nonfluorescent
GaP segments and fluorescent GaInP segments, we created a barcode
labeling system enabling the distinction of the nanowire morphological
and chemical properties using fluorescence microscopy. The GaInP photoluminescence
stability, combined with the fact that the nanowires can be coated
with different materials while retaining their fluorescence, make
these nanowires promising tools for biological and nanotoxicological
studies
Additional file 1 of Pulmonary toxicity and translocation of gallium phosphide nanowires to secondary organs following pulmonary exposure in mice
Supplementary Material 1: Experimental details and results of the pilot study and 3-months study. GaP NW synthesis and characterization in pilot study. Table S1: Pilot study design. Figure S1: Characterization of GaP NWs in the pilot study. Table S2: (Pilot study) Cellular composition of bronchoalveolar lavage 1 and 3 days after exposure to GaP NWs. Figure S2: (Pilot study) Histopathology of mouse lung 1 and 28 days after pulmonary exposure to GaP NWs. Table S3: 3-month study design. Figure S3: Additional darkfield of GaP NWs in tissues. Figure S4: Chemical identification by EDS of GaP NWs in lung tissue 1 day after exposure. Figure S5: SEM images of GaP NWs in lung tissue day 1 and 28 and 3 months post-exposure. Table S4: Diameter of gold nanoparticles and nanowires in vivo and in vitro. Figure S6, Table S5 and S6: Cellular composition of bronchoalveolar lavage 1, 3, 28 days and 3 months after exposure to GaP NWs, carbon black or MWCNT Mitsui-7. Figure S7 and Table S7: Genotoxicity in BAL cells, lung and liver tissue in 3-month study. Table S8. Mouse lung histopathology 1, 28 days and 3 months after intratracheal instillation of GaP NWs, incidence table. Table S9: Composition of phagolysosomal simulant fluid (PSF). Table S10: Composition of low-calcium Gamble’s solution