TY - JOUR
T1 - Near-Infrared Fluorescent Thiol-Organosilica Nanoparticles That Are Functionalized with IR-820 and Their Applications for Long-Term Imaging of in Situ Labeled Cells and Depth-Dependent Tumor in Vivo Imaging
AU - Nakamura, Michihiro
AU - Hayashi, Koichiro
AU - Nakamura, Junna
AU - Mochizuki, Chihiro
AU - Murakami, Takuya
AU - Miki, Hirokazu
AU - Ozaki, Shuji
AU - Abe, Masahiro
N1 - Funding Information:
We appreciate the assistance with electron microscopic observations by Dr. Koichi Udo in the Institute for Biomedical Research and Education and the technical support at the Yamaguchi University Center of Gene Research. This study was supported in part by JSPS KAKENHI (Grant-in-Aid for Scientific Research (B) (No. 20H03625), Grant-in-Aid for Scientific Research (C) (Nos. 21500409, 25350530, and 16K01358), Grant-in-Aid for Challenging Research (Exploratory) (No. 19K22534)), Research for Promoting Technological Seeds and Adaptable and Seamless Technology Transfer Program through target-driven R&D from Japan Science and Technology Agency (JST), and the JSPS Bilateral Programs (to M.N.)
Funding Information:
We appreciate the assistance with electron microscopic observations by Dr. Koichi Udo in the Institute for Biomedical Research and Education and the technical support at the Yamaguchi University Center of Gene Research. This study was supported in part by JSPS KAKENHI (Grant-in-Aid for Scientific Research (B) (No. 20H03625) Grant-in-Aid for Scientific Research (C) (Nos. 21500409, 25350530 and 16K01358), Grant-in-Aid for Challenging Research (Exploratory) (No. 19K22534)), Research for Promoting Technological Seeds and Adaptable and Seamless Technology Transfer Program through target-driven R&D from Japan Science and Technology Agency (JST), and the JSPS Bilateral Programs (to M.N.)
Publisher Copyright:
Copyright © 2020 American Chemical Society.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/9/8
Y1 - 2020/9/8
N2 - Thiol-organosilica nanoparticles that are internally functionalized with IR-820 (thiol-OS/IR820) were prepared via a one-pot process for near-infrared (NIR) fluorescence in vivo imaging. Thiol-OS/IR820 demonstrated broad-band emissive NIR fluorescence with multiple new fluorescent peaks that differed from those of the IR-820 molecule and upconversion fluorescence originated from thiol-OS. Thiol-OS/IR820 was biocompatible and did not show significant toxicity in vitro and in vivo. We conducted in vivo tracking of in situ labeled cells against subcutaneous xenograft cells. The in vivo imaging showed a migration and an accumulation of the in situ labeled cells to the site of xenograft cells. Then, a reduction of the grafted cells was observed after 3 weeks. Next, we conducted in vivo tumor imaging of a mouse with a subcutaneous xenograft tumor using intravenous administration of thiol-OS/IR820. Using three wavelengths of light emission, depth-dependent NIR fluorescence imaging of a mouse with a subcutaneous xenograft tumor was conducted. The accumulation of particles in the tumor tissue due to the enhanced permeability and retention (EPR) effect was observed depth-dependently. NIR fluorescence in vivo imaging using thiol-OS/IR820 is useful for long-term observation and shows substantial promise for the visualization of novel biological phenomena in vivo.
AB - Thiol-organosilica nanoparticles that are internally functionalized with IR-820 (thiol-OS/IR820) were prepared via a one-pot process for near-infrared (NIR) fluorescence in vivo imaging. Thiol-OS/IR820 demonstrated broad-band emissive NIR fluorescence with multiple new fluorescent peaks that differed from those of the IR-820 molecule and upconversion fluorescence originated from thiol-OS. Thiol-OS/IR820 was biocompatible and did not show significant toxicity in vitro and in vivo. We conducted in vivo tracking of in situ labeled cells against subcutaneous xenograft cells. The in vivo imaging showed a migration and an accumulation of the in situ labeled cells to the site of xenograft cells. Then, a reduction of the grafted cells was observed after 3 weeks. Next, we conducted in vivo tumor imaging of a mouse with a subcutaneous xenograft tumor using intravenous administration of thiol-OS/IR820. Using three wavelengths of light emission, depth-dependent NIR fluorescence imaging of a mouse with a subcutaneous xenograft tumor was conducted. The accumulation of particles in the tumor tissue due to the enhanced permeability and retention (EPR) effect was observed depth-dependently. NIR fluorescence in vivo imaging using thiol-OS/IR820 is useful for long-term observation and shows substantial promise for the visualization of novel biological phenomena in vivo.
UR - http://www.scopus.com/inward/record.url?scp=85090482286&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85090482286&partnerID=8YFLogxK
U2 - 10.1021/acs.chemmater.0c01414
DO - 10.1021/acs.chemmater.0c01414
M3 - Article
AN - SCOPUS:85090482286
SN - 0897-4756
VL - 32
SP - 7201
EP - 7214
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 17
ER -