Evaluation of topically applied copper(II) oxide nanoparticle cytotoxicity in human skin organ culture

被引:49
作者
Cohen, Dror [1 ]
Soroka, Yoram [2 ]
Ma'or, Zeev [1 ]
Oron, Miriam [1 ]
Portugal-Cohen, Meital [1 ]
Bregegere, Francois Menahem [2 ]
Berhanu, Deborah [3 ]
Valsami-Jones, Eugenia [3 ]
Hai, Noam [4 ]
Milner, Yoram [2 ]
机构
[1] Ahava Dead Sea Labs, Dead Sea, Israel
[2] Hebrew Univ Jerusalem, Dept Biol Chem, Myers Lab Skin Biol & Biochem, Jerusalem, Israel
[3] Nat Hist Museum, Dept Mineral, London SW7 5BD, England
[4] Atidim Med Ctr, Tel Aviv, Israel
关键词
Copper oxide; Nanoparticles; Skin organ culture; Inflammatory cytokines; Cytotoxicity; TOXICITY; PARTICLES; APOPTOSIS; STRESS; SIZE;
D O I
10.1016/j.tiv.2012.08.026
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 [卫生毒理学];
摘要
The increasing use of nano-sized materials in our environment, and in many consumer products, dictates new safety concerns. In particular, adequate experimental models are needed to evaluate skin toxicity of metal oxide ions, commonly found in cosmetic and dermatologic preparations. We have addressed the biological effects of topically applied copper oxide (CuO) nanoparticles in human skin organ cultures, using light and electron microscopy, and biochemical tests. Nanoparticles were more toxic than microsized particles, and their effects were stronger when supplied in growth medium than in topical application. Still topically applied CuO nanoparticles induced inflammatory cytokine secretion and necrosis, especially in epidermis deprived of its protective cornea. Since nanoparticle penetration was not seen, we propose that they may adhere to skin surface, react with the local acidic environment, and generate soluble ions that make their way to inner sites. This work illustrates the abilities of skin organ culture to evaluate the biological effects of topically-applied materials on skin in vitro. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:292 / 298
页数:7
相关论文
共 24 条
[1]
Nanomaterials and nanoparticles: Sources and toxicity [J].
Buzea, Cristina ;
Pacheco, Ivan I. ;
Robbie, Kevin .
BIOINTERPHASES, 2007, 2 (04) :MR17-MR71
[2]
Copper oxide nanoparticles induce oxidative stress and cytotoxicity in airway epithelial cells [J].
Fahmy, Baher ;
Cormier, Stephania A. .
TOXICOLOGY IN VITRO, 2009, 23 (07) :1365-1371
[3]
Functional and immunocytochemical identification of glutamate autoreceptors of an NMDA type in crayfish neuromuscular junction [J].
Feinstein, N ;
Parnas, D ;
Parnas, H ;
Dudel, J ;
Parnas, I .
JOURNAL OF NEUROPHYSIOLOGY, 1998, 80 (06) :2893-2899
[4]
Copper toxicity, oxidative stress, and antioxidant nutrients [J].
Gaetke, LM ;
Chow, CK .
TOXICOLOGY, 2003, 189 (1-2) :147-163
[5]
Induction of inflammation in vascular endothelial cells by metal oxide nanoparticles: Effect of particle composition [J].
Gojova, Andrea ;
Guo, Bing ;
Kota, Rama S. ;
Rutledge, John C. ;
Kennedy, Ian M. ;
Barakat, Abdul I. .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2007, 115 (03) :403-409
[6]
Toxicity of metal oxide nanoparticles in mammalian cells [J].
Jeng, Hueiwang Anna ;
Swanson, James .
JOURNAL OF ENVIRONMENTAL SCIENCE AND HEALTH PART A-TOXIC/HAZARDOUS SUBSTANCES & ENVIRONMENTAL ENGINEERING, 2006, 41 (12) :2699-2711
[7]
Copper oxide nanoparticles are highly toxic:: A comparison between metal oxide nanoparticles and carbon nanotubes [J].
Karlsson, Hanna L. ;
Cronholm, Pontus ;
Gustafsson, Johanna ;
Moeller, Lennart .
CHEMICAL RESEARCH IN TOXICOLOGY, 2008, 21 (09) :1726-1732
[8]
Size-dependent toxicity of metal oxide particles-A comparison between nano- and micrometer size [J].
Karlsson, Hanna L. ;
Gustafsson, Johanna ;
Cronholm, Pontus ;
Moller, Lennart .
TOXICOLOGY LETTERS, 2009, 188 (02) :112-118
[9]
APPLICATION OF THE MTT COLORIMETRIC ASSAY TO MEASURE CYTOTOXIC EFFECTS OF PHENOLIC-COMPOUNDS ON ESTABLISHED RAT DENTAL-PULP CELLS [J].
KASUGAI, S ;
HASEGAWA, N ;
OGURA, H .
JOURNAL OF DENTAL RESEARCH, 1991, 70 (02) :127-130
[10]
HYDROXYL RADICAL AND SINGLET OXYGEN PRODUCTION AND DNA DAMAGE INDUCED BY CARCINOGENIC METAL-COMPOUNDS AND HYDROGEN-PEROXIDE [J].
KAWANISHI, S ;
INOUE, S ;
YAMAMOTO, K .
BIOLOGICAL TRACE ELEMENT RESEARCH, 1989, 21 :367-372