TY - JOUR
T1 - Uptake and Intracellular Fate of Fluorophore Labeled Metal-Organic-Framework (MOF) Nanoparticles
AU - Liu, Ziyao
AU - Zimpel, Andreas
AU - Lächelt, Ulrich
AU - Pozzi, Maria
AU - Gonzalez, Marta Gallego
AU - Chakraborty, Indranath
AU - Wuttke, Stefan
AU - Feliu, Neus
AU - Parak, Wolfgang J.
N1 - Publisher Copyright:
© 2023 The Authors. Co-published by Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, and American Chemical Society.
PY - 2023/10/20
Y1 - 2023/10/20
N2 - The uptake and the fate of Zr-based metal-organic-framework nanoparticles labeled with organic fluorophores in HeLa cells has been monitored with fluorescence detection and elemental analysis. The nanoparticles have been selected as a model system of carrier nanoparticles (here Zr-based metal-organic-framework nanoparticles) with integrated cargo molecules (here organic fluorophores), with aze that does not allow for efficient exocytosis, a material which only partly degrades under acidic conditions as present in endosomes/lysosomes, and with limited colloidal stability. Data show that, for Zr-based metal-organic-framework nanoparticles of 40 nm size as investigated here, the number of nanoparticles per cells decreases faster due to particle redistribution upon proliferation than due to nanoparticle exocytosis and that, thus, also for this system, exocytosis is not an efficient pathway for clearance of the nanoparticles from the cells.
AB - The uptake and the fate of Zr-based metal-organic-framework nanoparticles labeled with organic fluorophores in HeLa cells has been monitored with fluorescence detection and elemental analysis. The nanoparticles have been selected as a model system of carrier nanoparticles (here Zr-based metal-organic-framework nanoparticles) with integrated cargo molecules (here organic fluorophores), with aze that does not allow for efficient exocytosis, a material which only partly degrades under acidic conditions as present in endosomes/lysosomes, and with limited colloidal stability. Data show that, for Zr-based metal-organic-framework nanoparticles of 40 nm size as investigated here, the number of nanoparticles per cells decreases faster due to particle redistribution upon proliferation than due to nanoparticle exocytosis and that, thus, also for this system, exocytosis is not an efficient pathway for clearance of the nanoparticles from the cells.
KW - exocytosis
KW - fate of nanoparticles
KW - intracellular degradation
KW - metal organic framework nanoparticles
KW - nanoparticle endocytosis
KW - proliferation
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U2 - 10.1021/envhealth.3c00075
DO - 10.1021/envhealth.3c00075
M3 - Article
AN - SCOPUS:85183497344
SN - 2833-8278
VL - 1
SP - 270
EP - 277
JO - Environment and Health
JF - Environment and Health
IS - 4
ER -