Small-angle X-ray scattering to quantify the incorporation and analyze the disposition of magnetic nanoparticles inside cells

被引:4
作者
Coral, D. F. [1 ,2 ]
Soto, P. A. [3 ]
de Sousa, E. [1 ]
Brollo, M. E. F. [4 ]
Mera-Cordoba, J. A. [5 ]
Zelis, P. Mendoza [1 ]
Setton-Avruj, C. P. [3 ]
Roig, A. [6 ]
van Raap, M. B. Fernandez [1 ]
机构
[1] Univ Nacl La Plata UNLP, Fac Ciencias Exactas, Inst Fis Plata IFLP CONICET, Cc 67, RA-1900 La Plata, Argentina
[2] Univ Cauca, Dept Fis, Popayan, Colombia
[3] UBA CONICET, Fac Farm & Bioquim, Inst Quim & Fisicoquim Biol Alejandro Paladini, Buenos Aires, DF, Argentina
[4] Inst Mat Sci Madrid ICMM CSIC, Dept Energy Environm & Hlth, Madrid, Spain
[5] Univ CESMAG, Pasto, Colombia
[6] Inst Ciencia Mat Barcelona ICMAB CSIC, Campus UAB, Bellaterra 08193, Spain
关键词
Superparamagnetic nanoparticles; Nanoflowers; Iron oxide; SAXS; small angle X-ray scattering; Synchrotron radiation; soft mater; A549; B16F0; cell up-take; IRON-OXIDE NANOPARTICLES; INTRACELLULAR BIODEGRADATION; DIPOLAR INTERACTIONS; SIZE; EFFICIENCY; SAXS; NANOSTRUCTURE; AGGREGATION; ACTUATION; IDENTITY;
D O I
10.1016/j.jcis.2021.09.165
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Access to detailed information on cells loaded with nanoparticles with nanoscale precision is of a long-standing interest in many areas of nanomedicine. In this context, designing a single experiment able to provide statistical mean data from a large number of living unsectioned cells concerning information on the nanoparticle size and aggregation inside cell endosomes and accurate nanoparticle cell up-take is of paramount importance. Small-angle X-ray scattering (SAXS) is presented here as a tool to achieve such relevant data. Experiments were carried out in cultures of B16F0 murine melanoma and A549 human lung adenocarcinoma cell lines loaded with various iron oxide nanostructures displaying distinctive structural characteristics. Five systems of water-dispersible magnetic nanoparticles (MNP) of different size, polydispersity and morphology were analyzed, namely, nearly monodisperse MNP with 11 and 13 nm mean size coated with meso-2,3-dimercaptosuccinic acid, more polydisperse 6 nm colloids coated with citric acid and two nanoflowers (NF) systems of 24 and 27 nm in size resulting from the aggregation of 8 nm MNP. Up-take was determined for each system using B16F0 cells. Here we show that SAXS pattern provides high resolution information on nanoparticles disposition inside endosomes of the cytoplasm through the structure factor analysis, on nanoparticles size and dispersity after their incorporation by the cell and on up-take quantification from the extrapolation of the intensity in absolute scale to null scattering vector. We also report on the cell culture preparation to reach sensitivity for the observation of MNP inside cell endosomes using high brightness SAXS synchrotron source. Our results show that SAXS can become a valuable tool for analyzing MNP in cells and tissues. (C) 2021 Elsevier Inc. All rights reserved.
引用
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页码:1 / 12
页数:12
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