TY - JOUR
T1 - High-Contrast Imaging of Nanodiamonds in Cells by Energy Filtered and Correlative Light-Electron Microscopy
T2 - Toward a Quantitative Nanoparticle-Cell Analysis
AU - Han, Sheng
AU - Raabe, Marco
AU - Hodgson, Lorna
AU - Mantell, Judith
AU - Verkade, Paul
AU - Lasser, Theo
AU - Landfester, Katharina
AU - Weil, Tanja
AU - Lieberwirth, Ingo
PY - 2019/3/13
Y1 - 2019/3/13
N2 - Fluorescent nanodiamonds (fNDs) represent an emerging class of nanomaterials offering great opportunities for ultrahigh resolution imaging, sensing and drug delivery applications. Their biocompatibility, exceptional chemical and consistent photostability renders them particularly attractive for correlative light-electron microscopy studies providing unique insights into nanoparticle-cell interactions. Herein, we demonstrate a stringent procedure to image and quantify fNDs with a high contrast down to the single particle level in cells. Individual fNDs were directly visualized by energy-filtered transmission electron microscopy, that is, inside newly forming, early endosomal vesicles during their cellular uptake processes as well as inside cellular organelles such as a mitochondrion. Furthermore, we demonstrate the unequivocal identification, localization, and quantification of individual fNDs in larger fND clusters inside intracellular vesicles. Our studies are of great relevance to obtain quantitative information on nanoparticle trafficking and their various interactions with cells, membranes, and organelles, which will be crucial to design-improved sensors, imaging probes, and nanotherapeutics based on quantitative data.
AB - Fluorescent nanodiamonds (fNDs) represent an emerging class of nanomaterials offering great opportunities for ultrahigh resolution imaging, sensing and drug delivery applications. Their biocompatibility, exceptional chemical and consistent photostability renders them particularly attractive for correlative light-electron microscopy studies providing unique insights into nanoparticle-cell interactions. Herein, we demonstrate a stringent procedure to image and quantify fNDs with a high contrast down to the single particle level in cells. Individual fNDs were directly visualized by energy-filtered transmission electron microscopy, that is, inside newly forming, early endosomal vesicles during their cellular uptake processes as well as inside cellular organelles such as a mitochondrion. Furthermore, we demonstrate the unequivocal identification, localization, and quantification of individual fNDs in larger fND clusters inside intracellular vesicles. Our studies are of great relevance to obtain quantitative information on nanoparticle trafficking and their various interactions with cells, membranes, and organelles, which will be crucial to design-improved sensors, imaging probes, and nanotherapeutics based on quantitative data.
KW - Correlative light electron microscopy
KW - energy-filtered transmission electron microscopy
KW - nanodiamond
KW - nanoparticle quantification
KW - particle-cell interactions
UR - https://www.scopus.com/pages/publications/85062790815
U2 - 10.1021/acs.nanolett.9b00752
DO - 10.1021/acs.nanolett.9b00752
M3 - Letter (Academic Journal)
C2 - 30810045
AN - SCOPUS:85062790815
SN - 1530-6984
VL - 19
SP - 2178
EP - 2185
JO - Nano Letters
JF - Nano Letters
IS - 3
ER -