TY - JOUR
T1 - Synthesis and characterization of magnetic nanoparticles coated with polystyrene sulfonic acid for biomedical applications
AU - Chen, Bo Wei
AU - He, Yun Chi
AU - Sung, Shian Ying
AU - Le, Trang Thi Huynh
AU - Hsieh, Chia Ling
AU - Chen, Jiann Yeu
AU - Wei, Zung Hang
AU - Yao, Da Jeng
N1 - Funding Information:
Taiwan Ministry of Science and Technology [grants MOST 105-2628-M-007-002-MY3, MOST 104-2221-E-007-015-MY4, MOST 105-2112-M-007-025-MY3 and MOST 107-2320-B-038-057-], and ?TMU Research Center of Cancer Translational Medicine? from Featured Areas Research Center Program within the framework of the Higher Education Sprout Project by Taiwan Ministry of Education (MOE) financially supported this work. The MNP characterization of TGA, SQUID and TEM were supported from the following projects: Taiwan Ministry of Science and Technology [grants MOST 108-2731-M-007-001-, MOST 108-2731-M-007-001 and MOST 108-2731-M-009-001-], respectively. The XRD and FTIR characterization was supported by Instrumentation Center at National Tsing Hua University (Hsinchu, Taiwan). The characterization of Raman spectra was supported by Center for Advanced Science and Technology (CAST) and Innovation and Development Center of Sustainable Agriculture (IDCSA) in National Chung Hsing University (Taichung, Taiwan). This manuscript was edited by Wallace Academic Editing.
Publisher Copyright:
© 2020, © 2020 The Author(s). Published by National Institute for Materials Science in partnership with Taylor & Francis Group.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/1/31
Y1 - 2020/1/31
N2 - The development of novel magnetic nanoparticles (MNPs) with satisfactory biocompatibility for biomedical applications has been the subject of extensive exploration over the past two decades. In this work, we synthesized superparamagnetic iron oxide MNPs coated with polystyrene sulfonic acid (PSS-MNPs) and with a conventional co-precipitation method. The core size and hydrodynamic diameter of the PSS-MNPs were determined as 8–18 nm and 50–200 nm with a transmission electron microscopy and dynamic light scattering, respectively. The saturation magnetization of the particles was measured as 60 emu g−1 with a superconducting quantum-interference-device magnetometer. The PSS content in the PSS-MNPs was 17% of the entire PSS-MNPs according to thermogravimetric analysis. Fourier-transform infrared spectra were recorded to detect the presence of SO3− groups, which confirmed a successful PSS coating. The structural properties of the PSS-MNPs, including the crystalline lattice, composition and phases, were characterized with an X-ray powder diffractometer and 3D nanometer-scale Raman microspectrometer. MTT assay and Prussian-blue staining showed that, although PSS-MNPs caused no cytotoxicity in both NIH-3T3 mouse fibroblasts and SK-HEP1 human liver-cancer cells up to 1000 μg mL−1, SK-HEP1 cells exhibited significantly greater uptake of PSS-MNPs than NIH-3T3 cells. The low cytotoxicity and high biocompatibility of PSS-MNPs in human cancer cells demonstrated in the present work might have prospective applications for drug delivery.
AB - The development of novel magnetic nanoparticles (MNPs) with satisfactory biocompatibility for biomedical applications has been the subject of extensive exploration over the past two decades. In this work, we synthesized superparamagnetic iron oxide MNPs coated with polystyrene sulfonic acid (PSS-MNPs) and with a conventional co-precipitation method. The core size and hydrodynamic diameter of the PSS-MNPs were determined as 8–18 nm and 50–200 nm with a transmission electron microscopy and dynamic light scattering, respectively. The saturation magnetization of the particles was measured as 60 emu g−1 with a superconducting quantum-interference-device magnetometer. The PSS content in the PSS-MNPs was 17% of the entire PSS-MNPs according to thermogravimetric analysis. Fourier-transform infrared spectra were recorded to detect the presence of SO3− groups, which confirmed a successful PSS coating. The structural properties of the PSS-MNPs, including the crystalline lattice, composition and phases, were characterized with an X-ray powder diffractometer and 3D nanometer-scale Raman microspectrometer. MTT assay and Prussian-blue staining showed that, although PSS-MNPs caused no cytotoxicity in both NIH-3T3 mouse fibroblasts and SK-HEP1 human liver-cancer cells up to 1000 μg mL−1, SK-HEP1 cells exhibited significantly greater uptake of PSS-MNPs than NIH-3T3 cells. The low cytotoxicity and high biocompatibility of PSS-MNPs in human cancer cells demonstrated in the present work might have prospective applications for drug delivery.
KW - 301 Chemical syntheses / processing
KW - 503 TEM
KW - 504 X-ray / Neutron diffraction and scattering
KW - 505 Optical / Molecular spectroscopy
KW - biocompatibility
KW - biomedical applications
KW - Magnetic nanoparticle
KW - polystyrene sulfonic acid (PSS)
KW - SEM; 203 Magnetics / Spintronics / Superconductors
KW - STEM
KW - superparamagnetic iron oxide (SPIO)
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U2 - 10.1080/14686996.2020.1790032
DO - 10.1080/14686996.2020.1790032
M3 - Article
AN - SCOPUS:85088449148
SN - 1468-6996
VL - 21
SP - 471
EP - 481
JO - Science and Technology of Advanced Materials
JF - Science and Technology of Advanced Materials
IS - 1
ER -