Cellular and Molecular Toxicity of Iron Oxide Nanoparticles

被引:46
作者
Laffon, Blanca [1 ]
Fernandez-Bertolez, Natalia [1 ,2 ]
Costa, Carla [3 ,4 ]
Brandao, Fatima [3 ,4 ]
Teixeira, Joao Paulo [3 ,4 ]
Pasaro, Eduardo [1 ]
Valdiglesias, Vanessa [1 ,4 ]
机构
[1] Univ A Coruna, DICOMOSA Grp, Dept Psychol, Area Psychobiol, La Coruna, Spain
[2] Univ A Coruna, Dept Cell & Mol Biol, La Coruna, Spain
[3] Portuguese Natl Inst Hlth, Dept Environm Hlth, Porto, Portugal
[4] Univ Porto, ISPUP EPIUnit, Porto, Portugal
来源
CELLULAR AND MOLECULAR TOXICOLOGY OF NANOPARTICLES | 2018年 / 1048卷
关键词
Iron oxide nanoparticles; Cell viability; Mitochondrial alterations; Oxidative damage; Cell membrane impairment; Genomic alterations; IN-VITRO CYTOTOXICITY; NEURAL STEM-CELLS; MAGNETIC NANOPARTICLES; OXIDATIVE STRESS; MITOCHONDRIAL DAMAGE; FE3O4; NANOPARTICLES; DEPENDENT TOXICITY; CONTRAST AGENTS; GENE-EXPRESSION; CANCER-CELLS;
D O I
10.1007/978-3-319-72041-8_12
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Iron oxide nanoparticles (ION) have attracted much attention because of their particular physico-chemical properties, including superparamagnetism. These features make them suitable for many purposes and several interesting biomedical applications, such as to increase contrast in magnetic resonance imaging (MRI), as drug delivery systems and as hyperthermia agents. However, they have also shown to be easily accumulated in diverse tissues and induce toxicity at different levels. This chapter reviews the different cellular and molecular effects induced by ION reported from in vitro studies with human and non-human cell lines. Those effects are mainly dependent on ION type and concentration, time of exposure, presence and nature of coating, and cell type evaluated. They include decreases in viability, plasmatic membrane disruption, oxidative damage, mitochondrial alterations, cell cycle impairments, cytoskeleton disruption, cell death, and alterations in cell motility, and in cell integrity. Despite these negative effects, the numerous advantages of ION together with their promising applications in biomedicine, make it necessary to clearly define their toxicity in order to discard potential health risks and to reach optimal benefits of their use.
引用
收藏
页码:199 / 213
页数:15
相关论文
共 139 条
[1]   Targeted nanoparticle enhanced proapoptotic peptide as potential therapy for glioblastoma [J].
Agemy, Lilach ;
Friedmann-Morvinski, Dinorah ;
Kotamraju, Venkata Ramana ;
Roth, Lise ;
Sugahara, Kazuki N. ;
Girard, Olivier M. ;
Mattrey, Robert F. ;
Verma, Inder M. ;
Ruoslahti, Erkki .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (42) :17450-17455
[2]   Cobalt iron oxide nanoparticles induce cytotoxicity and regulate the apoptotic genes through ROS in human liver cells (HepG2) [J].
Ahamed, Maqusood ;
Akhtar, Mohd Javed ;
Khan, M. A. Majeed ;
Alhadlaq, Hisham A. ;
Alshamsan, Aws .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2016, 148 :665-673
[3]   Induction of oxidative stress, DNA damage, and apoptosis in a malignant human skin melanoma cell line after exposure to zinc oxide nanoparticles [J].
Alarifi, Saud ;
Ali, Daoud ;
Alkahtani, Saad ;
Verma, Ankit ;
Ahamed, Maqusood ;
Ahmed, Mukhtar ;
Alhadlaq, Hisham A. .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2013, 8 :983-993
[4]   Silica-coated super paramagnetic iron oxide nanoparticles (SPION) as biocompatible contrast agent in biomedical photoacoustics [J].
Alwi, Rudolf ;
Telenkov, Sergey ;
Mandelis, Andreas ;
Leshuk, Timothy ;
Gu, Frank ;
Oladepo, Sulayman ;
Michaelian, Kirk .
BIOMEDICAL OPTICS EXPRESS, 2012, 3 (10) :2500-2509
[5]   Nanoparticles in the clinic [J].
Anselmo, Aaron C. ;
Mitragotri, Samir .
BIOENGINEERING & TRANSLATIONAL MEDICINE, 2016, 1 (01) :10-29
[6]   Improved cytotoxicity and preserved level of cell death induced in colon cancer cells by doxorubicin after its conjugation with iron-oxide magnetic nanoparticles [J].
Augustin, Ewa ;
Czubek, Bartlomiej ;
Nowicka, Anna M. ;
Kowalczyk, Agata ;
Stojek, Zbigniew ;
Mazerska, Zofia .
TOXICOLOGY IN VITRO, 2016, 33 :45-53
[7]   Age Modulates Fe3O4 Nanoparticles Liver Toxicity: Dose-Dependent Decrease in Mitochondrial Respiratory Chain Complexes Activities and Coupling in Middle-Aged as Compared to Young Rats [J].
Baratli, Yosra ;
Charles, Anne-Laure ;
Wolff, Valerie ;
Ben Tahar, Lotfi ;
Smiri, Leila ;
Bouitbir, Jamal ;
Zoll, Joffrey ;
Sakly, Mohsen ;
Auger, Cyril ;
Vogel, Thomas ;
Abdelmelek, Hafedh ;
Tebourbi, Olfa ;
Geny, Bernard .
BIOMED RESEARCH INTERNATIONAL, 2014, 2014
[8]   Cell motility of neural stem cells is reduced after SPIO-labeling, which is mitigated after exocytosis [J].
Berman, Stacey M. Cromer ;
Kshitiz ;
Wang, C. Joanne ;
Orukari, Inema ;
Levchenko, Andre ;
Bulte, Jeff W. M. ;
Walczak, Piotr .
MAGNETIC RESONANCE IN MEDICINE, 2013, 69 (01) :255-262
[9]   Dextran and albumin derivatised iron oxide nanoparticles: influence on fibroblasts in vitro [J].
Berry, CC ;
Wells, S ;
Charles, S ;
Curtis, ASG .
BIOMATERIALS, 2003, 24 (25) :4551-4557
[10]   Cell response to dextran-derivatised iron oxide nanoparticles post internalisation [J].
Berry, CC ;
Wells, S ;
Charles, S ;
Aitchison, G ;
Curtis, ASG .
BIOMATERIALS, 2004, 25 (23) :5405-5413