References
- L.K. Adams, D.Y. Lyon, P.J. Alvarez, Comparative eco-toxicity of nanoscale TiO2, SiO2, and ZnO water suspensions. Water Res. 40(19), 3527-3532 (2006) https://doi.org/10.1016/j.watres.2006.08.004
- S. Ahmed, M. Ahmad, B.L. Swami, S. Ikram, A review on plants extract mediated synthesis of silver nanoparticles for antimicrobial applications: A green expertise. J. Adv. Res. 7, 17-28 (2016) https://doi.org/10.1016/j.jare.2015.02.007
- M. Allegri, M.G. Bianchi, M. Chiu, J. Varet, A.L. Costa, S. Ortelli, M. Blosi, O. Bussolati, C.A. Poland, E. Bergamaschi, Shape-related toxicity of titanium dioxide Nanofibres. PLoS One 11(3), e0151365 (2016) https://doi.org/10.1371/journal.pone.0151365
- J.H.E. Arts et al., A decision-making framework for the grouping and testing of nanomaterials (DF4nanoGrouping). Regul. Toxicol. Pharmacol. 71(2), S1-S27 (2015) https://doi.org/10.1016/j.yrtph.2015.03.007
- P.V. Asharani, Y.L. Wu, Z. Gong, S. Valiyaveettil, Toxicity of silver nanoparticles in zebrafish models. Nanotechnology. 19 (2008). https://doi.org/10.1088/0957-4484/19/25/255102
- L. Belyanskaya, S. Weigel, C. Hirsch, U. Tobler, H. Krug, P. Wick, Effects of carbon nanotubes on primary neurons and glial cells. Neurotoxicology 30, 702-711 (2009) https://doi.org/10.1016/j.neuro.2009.05.005
- J. Beranova, G. Seydlova, H. Kozak, O. Benada, R. Fiser, A. Artemenko, I. Konopasek, A. Kromka, Sensitivity of bacteria to diamond nanoparticles of various size differs in gram-positive and gram-negative cells. FEMS Microbiol. Lett. 351(2), 179-186 (2014) https://doi.org/10.1111/1574-6968.12373
- J.S. Bozich, S.E. Lohse, M.D. Torelli, C.J. Murphy, R.J. Hamers, R.D. Klaper, Surface chemistry, charge and ligand type impact the toxicity of gold nanoparticles to Daphnia magna. Environ Sci: Nano. 1, 260-270 (2014) https://doi.org/10.1039/C4EN00006D
- M. Cobaleda-Siles, A.P. Guillamon, C. Delpivo, S. Vazquez-Campos, V.F. Puntes, Safer by design strategies. IOP Conf. Ser: J. Phys. (2017). https://doi.org/10.1088/1742-6596/838/1/012016
- S.A. Dahoumane, E.K. Wujcik, C. Jeffryes, Noble metal, oxide and chalcogenide-based nanomaterials from scalable phototrophic culture systems. Enzym. Microb. Technol. 95, 13-27 (2016) https://doi.org/10.1016/j.enzmictec.2016.06.008
- J. Duan et al., Inflammation-coagulation response and thrombotic effects induced by silica nanoparticles in zebrafish embryos. Nanotoxicology 12, 470-484 (2018) https://doi.org/10.1080/17435390.2018.1461267
-
A. Erdem, D. Metzler, D.K. Cha, C.P. Huang, The short-term toxic effects of
$TiO_2$ nanoparticles toward bacteria through viability, cellular respiration, and lipid peroxidation. Environ. Sci. Pollut. Res. Int. 22(22), 17917-17924 (2015). https://doi.org/10.1007/s11356-015-5018-1 - V.E. Fako, D.Y. Furgeson, Zebrafish as a correlative and predictive model for assessing biomaterial nanotoxicity. Adv Drug Deliver Rev. 61, 478-486 (2009) https://doi.org/10.1016/j.addr.2009.03.008
- B. Fubini, M. Ghiazza, I. Fenoglio, Physico-chemical features of engineered nanoparticles relevant to their toxicity. Nanotoxicology 4, 347-363 (2010) https://doi.org/10.3109/17435390.2010.509519
- M.A. Gatoo et al., Physicochemical properties of nanomaterials: Implication in associated toxic manifestations. Biomed. Res. Int. (2014). https://doi.org/10.1155/2014/498420
- S. George et al., Use of a rapid cytotoxicity screening approach to engineer a safer zinc oxide nanoparticle through iron doping. ACS Nano 4, 15-29 (2010) https://doi.org/10.1021/nn901503q
- J. Geys et al., Acute toxicity and Prothrombotic effects of quantum dots: Impact of surface charge. Environ. Health Perspect. 116, 1607-1613 (2008) https://doi.org/10.1289/ehp.11566
- L.M. Gilbertson et al., Toward safer multi-walled carbon nanotube design: Establishing a statistical model that relates surface charge and embryonic zebrafish mortality. Nanotoxicology 10(1), 10-19 (2016)
- H. Godwin et al., Nanomaterial categorization for assessing risk potential to facilitate regulatory decision-making. ACS Nano 9(4), 3409-3417 (2015) https://doi.org/10.1021/acsnano.5b00941
- R.J. Griffitt, J. Luo, J. Gao, J.C. Bonzongo, D.S. Barber, Effects of particle composition and species on toxicity of metallic nanomaterials in aquatic organisms. Environ. Toxicol. Chem. 27(9), 1972-1978 (2008) https://doi.org/10.1897/08-002.1
- R.D. Handy, G. Al-Bairuty, A. Al-Jubory, C.S. Ramsden, D. Boyle, B.J. Shaw, T.B. Henry, Effects of manufactured nanomaterials on fishes: A target organ and body systems physiology approach. J. Fish Biol. 79(4), 821-853 (2011) https://doi.org/10.1111/j.1095-8649.2011.03080.x
- R.D. Handy et al., Practical considerations for conducting ecotoxicity test methods with manufactured nanomaterials: What have we learnt so far? Ecotoxicology. 21(4), 933-972 (2012) https://doi.org/10.1007/s10646-012-0862-y
- S.L. Harper, J.L. Carriere, J.M. Miller, J.E. Hutchison, B.L.S. Maddux, R.L. Tanguay, Systematic evaluation of nanomaterial toxicity: Utility of standardized materials and rapid assays. ACS Nano 5, 4688-4697 (2011) https://doi.org/10.1021/nn200546k
- T.S. Hauck, A.A. Ghazani, W.C.W. Chan, Assessing the effect of surface chemistry on gold nanorod uptake, toxicity, and gene expression in mammalian cells. Small. 4, 153 (2008) https://doi.org/10.1002/smll.200700217
- O.D. Hendrickson, I.V. Safenkova, A.V. Zherdev, B.B. Dzantiev, V.O. Popov, Methods of detection and identification of manufactured nanoparticles. Biofizika. 56(6), 965-994 (2011)
- G. Jia, H. Wang, L. Yan, X. Wang, R. Pei, T. Yan, Y. Zhao, X. Guo, Cytotoxicity of carbon nanomaterials: Single-Wall nanotube, Multi-Wall nanotube, and fullerene. Environ. Sci. Technol. 39, 1378-1383 (2005) https://doi.org/10.1021/es048729l
- M. Kitching, M. Ramani, E. Marsili, Fungal biosynthesis of gold nanoparticles: Mechanism and scale up. Microb. Biotechnol. 8, 904-917 (2015) https://doi.org/10.1111/1751-7915.12151
- P. Korshed, L. Li, Z. Liu, T. Wang, The molecular mechanisms of the antibacterial effect of picosecond laser generated silver nanoparticles and their toxicity to human cells. PLoS One 11(8), e0160078 (2016) https://doi.org/10.1371/journal.pone.0160078
- J. Kostal, A. Voutchkova-Kostal, P.T. Anastas, J.B. Zimmerman, Identifying and designing chemicals with minimal acute aquatic toxicity. Proc. Natl. Acad. Sci. 112(20), 6289-6294 (2015) https://doi.org/10.1073/pnas.1314991111
- A. Kraegeloh, B. Suarez-Merino, T. Sluijters, C. Micheletti, Implementation of safe-by-Design for Nanomaterial Development and Safe Innovation: Why we need a comprehensive approach. Nanomaterials (Basel). 8(4), 239 (2018) https://doi.org/10.3390/nano8040239
- W.G. Kreyling, M. Semmler-Behnke, W. Moller, Ultrafine particle-lung interactions: Does size matter? J. Aerosol Med. 19(1), 74-83 (2006) https://doi.org/10.1089/jam.2006.19.74
- J.S. Lee, C.-H. Tung, Enhancing the cellular delivery of nanoparticles using lipooligoarginine peptides. Adv. Funct. Mater. 22, 4924-4930 (2012) https://doi.org/10.1002/adfm.201201345
- K.J. Lee, L.M. Browning, P.D. Nallathamby, X.H. Xu, Study of charge-dependent transport and toxicity of peptide-functionalized silver nanoparticles using zebrafish embryos and single nanoparticle plasmonic spectroscopy. Chem. Res. Toxicol. 26, 904-917 (2013) https://doi.org/10.1021/tx400087d
- R. Li et al., Surface interactions with compartmentalized cellular phosphates explain rare earth oxide nanoparticle Hazard and provide opportunities for safer design. ACS Nano 8(2), 1771-1783 (2014) https://doi.org/10.1021/nn406166n
- X. Li et al., Evaluation of toxic effects of CdTe quantum dots on the reproductive system in adult male mice. Biomaterials 96, 24-32 (2016) https://doi.org/10.1016/j.biomaterials.2016.04.014
- Y. Li, Y. Liu, Y. Fu, T. Wei, L. Le Guyader, G. Gao, R. Liu, Y. Chang, C. Chen, The triggering of apoptosis in macrophages by pristine graphene through the MAPK and TGF-Beta signaling pathways. Biomaterials 33, 402-411 (2012) https://doi.org/10.1016/j.biomaterials.2011.09.091
- Y. Liu et al., Understanding the toxicity of carbon nanotubes. Acc. Chem. Res. 46(3), 702-713 (2013) https://doi.org/10.1021/ar300028m
-
S.B. Lovern, J.R. Strickler, R. Klaper, Behavioral and physiological changes in Daphnia magna when exposed to nanoparticle suspensions (titanium dioxide,
$nano-C_{60}$ , and$C_{60}H_xC_{70}H_x$ ). Environ Sci Technol. 41(12), 4465-4470 (2007) https://doi.org/10.1021/es062146p -
M. Mahdavi, F. Namvar, M.B. Ahmad, R. Mohamad, Green biosynthesis and characterization of magnetic iron oxide (
$Fe_3O_4$ ) nanoparticles using seaweed (Sargassum muticum) aqueous extract. Molecules. 18, 5954-5964 (2013) https://doi.org/10.3390/molecules18055954 - P. Marckmann et al., Nephrogenic systemic fibrosis: Suspected causative role of gadodiamide used for contrast-enhanced magnetic resonance imaging. J. Am. Soc. Nephrol. 17(9), 2359-2362 (2006) 50 https://doi.org/10.1681/ASN.2006060601
- J. Me'rian, J. Gravier, F. Navarro, I. Texier, Fluorescent nanoprobes dedicated to in vivo imaging: From preclinical validations to clinical translation. Molecules. 17, 5564-5591 (2012) https://doi.org/10.3390/molecules17055564
- Moore M N, Do nanoparticles present ecotoxicological risks for the health of the aquatic environment? DOI: https://doi.org/10.1016/j.envint.2006.06.014
- T. Mustafa, Y. Zhang, F. Watanabe, et al., Iron oxide nanoparticle-based radio-frequency thermotherapy for human breast adenocarcinoma cancer cells. Biomater Sci 1, 870-880 (2013) https://doi.org/10.1039/c3bm60015g
- N.N.I. National Nanotechnology Initiative Environmental, Health, and Safety Reserach strategy. National Science and technology council committee on technology and the subcommittee on nanoscale science, engineering, and Technology. (2011). https://www.nano.gov/sites/default/files/pub_resource/nni_2011_ehs_research_strategy.pdf
- N.R.C, A Research Strategy for Environmental, Health, and Safety Aspects of Engineered Nanomaterials (National Research Council of The National Academies, Washington, D.C, 2012)
- H. Naatz et al., Safe-by-design of CuO nanoparticles via Fe-doping, cu-O bond lengths variation, and biological assessment in cells and zebrafish embryos. ACS Nano 11(1), 501-515 (2017) https://doi.org/10.1021/acsnano.6b06495
- D.A. Nedosekin, S. Foster, Z.A. Nima, A.S. Biris, E.I. Galanzha, V.P. Zharov, Photothermal confocal multicolor microscopy of nanoparticles and nanodrugs in live cells. Drug Metab. Rev. (2015). https://doi.org/10.3109/03602532.2015.1058818
- A. Nel, T. Xia, H. Meng, X. Wang, S. Lin, Z. Ji, H. Zhang, Nanomaterial toxicity testing in the 21st century: Use of a predictive toxicological approach and high-throughput screening. Acc. Chem. Res. 46, 607-621 (2013) https://doi.org/10.1021/ar300022h
- T. Niidome, M. Yamagata, Y. Okamoto, Y. Akiyama, H. Takahashi, T. Kawano, Y. Katayama, Y. Niidome, PEG-modified gold nanorods with a stealth character for in vivo applications. J. Control. Release 114, 343-347 (2006) https://doi.org/10.1016/j.jconrel.2006.06.017
- D.A. Notter, D.M. Mitrano, B. Nowack, Are nanosized or dissolved metals more toxic in the environment? A meta-analysis. Environ. Toxicol. Chem. 33(12), 2733-2739 (2014) https://doi.org/10.1002/etc.2732
- A. Ostrowski et al., Overview about the localization of nanoparticles in tissue and cellular context by different imaging techniques. Beilstein J. Nanotechnol. 6, 263-280 (2015) https://doi.org/10.3762/bjnano.6.25
- J. Palomaki, E. Valimaki, J. Sund, M. Vippola, P. Clausen, K. Jensen, K. Savolainen, S. Matikainen, H. Alenius, Long, needle-like carbon nanotubes and Asbestos activate the NLRP3 Inflammasome through a similar mechanism. ACS Nano 5, 6861-6870 (2011) https://doi.org/10.1021/nn200595c
- H.K. Patra, S. Banerjee, U. Chaudhuri, P. Lahiri, A.K. Dasgupta, Cell-selective response to gold nanoparticles. Nanomedicine. 3, 111-119 (2007) https://doi.org/10.1016/j.nano.2007.03.005
- E.J. Petersen, T.B. Henry, J. Zhao, R.I. MacCuspie, T.L. Kirschling, M.A. Dobrovolskaia, V. Hackley, B. Xing, J.C. White, Identification and avoidance of potential artifacts and misinterpretations in nanomaterial ecotoxicity measurements. Environ. Sci. Technol. 48, 4226-4246 (2014) https://doi.org/10.1021/es4052999
- C. Poland, R. Duffin, I. Kinloch, A. Maynard, W. Wallace, A. Seaton, V. Stone, S. Brown, W. Macnee, K. Donaldson, Carbon nanotubes introduced into the abdominal cavity of mice show Asbestos-like pathogenicity in a pilot study. Nat. Nanotechnol. 3, 423-428 (2008) https://doi.org/10.1038/nnano.2008.111
- A. Porter, M. Gass, J. Bendall, K. Muller, A. Goode, J. Skepper, P. Midgley, M. Welland, Uptake of noncytotoxic acid-treated single-walled carbon nanotubes into the cytoplasm of human macrophage cells. ACS Nano 3, 1485-1492 (2009) https://doi.org/10.1021/nn900416z
- K. Pulskamp, S. Diabate, H. Krug, Carbon nanotubes show no sign of acute toxicity but induce intracellular reactive oxygen species in dependence on contaminants. Toxicol. Lett. 168, 58-74 (2007) https://doi.org/10.1016/j.toxlet.2006.11.001
- Ramanathan A A and Aqra M A. An overview of the Green Road to the Synthesis of Nanoparticles. DOI: https://doi.org/10.9734/JMSRR/2019/46014
- L.Y. Rizzo, S.K. Golombek, M.E. Mertens, Y. Pan, D. Laaf, J. Broda, J. Jayapaul, D. Mockel, V. Subr, F. Kiessling, T. Lammers, In vivo nanotoxicity testing using the zebrafish embryo assay. J. Mater. Chem. B 1, 3918-3925 (2013) https://doi.org/10.1039/c3tb20528b
- Y. Sato, A. Yokoyama, K. Shibata, Y. Akimoto, S. Ogino, Y. Nodasaka, T. Kohgo, K. Tamura, T. Akasaka, M. Uo, K. Motomiya, B. Jeyadevan, M. Ishiguro, R. Hatakeyama, F. Watari, K. Tohji, Influence of length on cytotoxicity of multi-walled carbon nanotubes against human acute monocytic leukemia cell line THP-1 in vitro and subcutaneous tissue of rats in vivo. Mol. BioSyst. 1, 176-182 (2005) https://doi.org/10.1039/b502429c
- J.J. Scott-Fordsmand et al., A unified framework for nanosafety is needed. Nano Today 9(5), 546-549 (2014) https://doi.org/10.1016/j.nantod.2014.07.001
- H. Selck et al., Nanomaterials in the aquatic environment: An EU-USA perspective on the status of ecotoxicity testing, research priorities and challenges ahead. Environ. Toxicol. Chem. 35(5), 1055-1067 (2016). https://doi.org/10.1002/etc.3385
- G.A. Sotiriou et al., Engineering safer-by-design silica-coated ZnO nanorods with reduced DNA damage potential. Environ. Sci.: Nano. 1, 144-153 (2014) https://doi.org/10.1039/c3en00062a
- V. Stone et al., ITS-NANO-Prioritising nanosafety research to develop a stakeholder driven intelligent testing strategy. Part. Fibre Toxicol. 11(1), 9 (2014) https://doi.org/10.1186/1743-8977-11-9
- A. Takagi, A. Hirose, T. Nishimura, N. Fukumori, A. Ogata, N. Ohashi, S. Kitajima, J. Kanno, Induction of mesothelioma in p53+/mouse by intraperitoneal application of multi-wall carbon nanotube. J. Toxicol. Sci. 33, 105-116 (2008) https://doi.org/10.2131/jts.33.105
- H. Takahashi, Y. Niidome, T. Niidome, K. Kaneko, H. Kawasaki, S. Yamada, Modification of gold nanorods using phosphatidylcholine to reduce cytotoxicity. Langmuir. 22, 2-5 (2006) https://doi.org/10.1021/la0520029
- T. Theoreta, K.J. Wilkinson, Evaluation of enhanced darkfield microscopy and hyperspectral analysis to analyse the fate of silver nanoparticles in wastewaters. Anal. Methods 9, 3920-3928 (2017) https://doi.org/10.1039/C7AY00615B
- C.Y. Usenko, S.L. Harper, R.L. Tanguay, In vivo evaluation of carbon fullerene toxicity using embryonic zebrafish. Carbon. 45, 1891-1898 (2007) https://doi.org/10.1016/j.carbon.2007.04.021
- A. Valipoor et al., A comparative study about toxicity of CdSe quantum dots on reproductive system development of mice and controlling this toxicity by ZnS coverage. Nanomed. J. 2(4), 261-268 (2015)
- A. Voutchkova-Kostal, J. Kostal, K.A. Connors, B.W. Brooks, P.T. Anastas, J.B. Zimmerman, Toward rational molecular design for reduced chronic aquatic toxicity. Green Chem. 14, 1001-1008 (2012) https://doi.org/10.1039/c2gc16385c
- S. Wang, W. Lu, O. Tovmachenko, U.S. Rai, H. Yu, P.C. Ray, Challenge in understanding size and shape dependent toxicity of gold nanomaterials in human skin keratinocytes. Chem. Phys. Lett. 463(1-3), 145-149 (2008) https://doi.org/10.1016/j.cplett.2008.08.039
- P. Wick, P. Manser, L. Limbach, U. Dettlaff-Weglikowska, F. Krumeich, S. Roth, W. Stark, A. Bruinink, The degree and kind of agglomeration affect carbon nanotube cytotoxicity. Toxicol. Lett. 168, 121-131 (2007) https://doi.org/10.1016/j.toxlet.2006.08.019
- T. Wu, M. Tang, Toxicity of quantum dots on respiratory system. Inhal. Toxicol. International Forum for Respiratory Research 26, 128-139 (2014)
- T. Xia et al., Comparison of the mechanism of toxicity of zinc oxide and cerium oxide nanoparticles based on dissolution and oxidative stress properties. ACS Nano 2, 2121-2134 (2008) https://doi.org/10.1021/nn800511k
- T. Xia et al., Decreased dissolution of ZnO by iron doping yields nanoparticles with reduced toxicity in the rodent lung and zebrafish embryos. ACS Nano 5(2), 1223-1235 (2011) https://doi.org/10.1021/nn1028482
- K. Yamashita, Y. Yoshioka, K. Higashisaka, Y. Morishita, T. Yoshida, M. Fujimura, H. Kayamuro, H. Nabeshi, T. Yamashita, K. Nagano, Y. Abe, H. Kamada, Y. Kawai, T. Mayumi, T. Yoshikawa, N. Itoh, S. Tsunoda, Y. Tsutsumi, Carbon nanotubes elicit DNA damage and inflammatory response relative to their size and shape. Inflammation 33, 276-280 (2010) https://doi.org/10.1007/s10753-010-9182-7
- Y. Yang et al., Toxicity and biodistribution of aqueous synthesized ZnS and ZnO quantum dots in mice. Nanotoxicology 8, 107-116 (2014) https://doi.org/10.3109/17435390.2012.760014
- N. Ye et al., Dissolved organic matter and aluminum oxide nanoparticles synergistically cause cellular responses in freshwater microalgae. J. Environ. Sci. Health 53, 651-658 (2018) https://doi.org/10.1080/10934529.2018.1438814
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