84
Brannen KC, Chapin RE, Jacobs AC, Green ML (2016) Alternative models of developmental and
reproductive toxicity in pharmaceutical risk assessment and the 3Rs. ILAR J 57(2):144–156.
https://doi.org/10.1093/ilar/ilw026
Braydich-Stolle L, Hussain S, Schlager JJ, Hofmann MC (2005) In vitro cytotoxicity of nanoparticles in mammalian germline stem cells. Toxicol Sci 88(2):412–419. https://doi.org/10.1093/
toxsci/kfi256
Braydich-Stolle LK, Lucas B, Schrand A, Murdock RC, Lee T, Schlager JJ, Hussain SM, Hofmann
MC (2010) Silver nanoparticles disrupt GDNF/Fyn kinase signaling in spermatogonial stem
cells. Toxicol Sci 116(2):577–589. https://doi.org/10.1093/toxsci/kfq148
Busquet F, Strecker R, Rawlings JM, Belanger SE, Braunbeck T, Carr GJ, Cenijn P, Fochtman P,
Gourmelon A, Hübler N, Kleensang A, Knöbel M, Kussatz C, Legler J, Lillicrap A, MartínezJerónimo F, Polleichtner C, Rzodeczko H, Salinas E, Schneider KE, Scholz S, van den
Brandhof EJ, van der Ven LT, Walter-Rohde S, Weigt S, Witters H, Halder M (2014) OECD
validation study to assess intra- and inter-laboratory reproducibility of the zebrafish embryo
toxicity test for acute aquatic toxicity testing. Regul Toxicol Pharmacol 69(3):496–511. https://
doi.org/10.1016/j.yrtph.2014.05.018
Caldeira DF, Paulini F, Silva RC, Azevedo RB, Lucci CM (2017) In vitro exposure of bull sperm
cells to DMSA-coated maghemite nanoparticles does not affect cell functionality or structure.
Int J Hyperth 34(4):415–422. https://doi.org/10.1080/02656736.2017.1341646
Calienni MN, Feas DA, Igartúa DE, Chiaramoni NS, Alonso SDV, Prieto MJ (2017)
Nanotoxicological and teratogenic effects: a linkage between dendrimer surface charge and
zebrafish developmental stages. Toxicol Appl Pharmacol 337:1–11. https://doi.org/10.1016/j.
taap.2017.10.003
Campos VF, de Leon PM, Komninou ER, Dellagostin OA, Deschamps JC, Seixas FK, Collares T
(2011) NanoSMGT: transgene transmission into bovine embryos using halloysite clay nanotubes or nanopolymer to improve transfection efficiency. Theriogenology 76(8):1552–1560.
https://doi.org/10.1016/j.theriogenology.2011.06.027
Cartwright L, Poulsen MS, Nielsen HM, Pojana G, Knudsen LE, Saunders M, Rytting E (2012)
In vitro placental model optimization for nanoparticle transport studies. Int J Nanomedicine
7:497–510. https://doi.org/10.2147/IJN.S26601
Cattaneo AG (2018) Nanotoxicological evaluation in marine water ecosystem: a detailed review.
In: Kumar V, Dasgupta N, Ranjan S (eds) Environmental toxicity of nanomaterials. CRC Press,
Taylor and Francis Group, Boca Raton, USA. Chapter 3, pp 47–76
Celá P, Veselá B, Matalová E, Večeřa Z, Buchtová M (2014) Embryonic toxicity of nanoparticles.
Cells Tissues Organs 199(1):1–23. https://doi.org/10.1159/000362163
Chan W-H, Shiao N-H (2008) Cytotoxic effect of CdSe quantum dots on mouse embryonic development. Acta Pharmacol Sin 28(2):259–266. https://doi.org/10.1111/j.1745- 7254.2008.00743.x
Chen L, Qiu R, Li L (2014) The role of nanotechnology in induced pluripotent and embryonic stem
cell research. J Biomed Nanotechnol 10:3431–3461. https://doi.org/10.1166/jbn.2014.2043
Chen Y, Hu X, Sun J, Zhou Q (2015) Specific nanotoxicity of graphene oxide during zebrafish embryogenesis. Nanotoxicology 10(1):42–52. https://doi.org/10.3109/1743539
0.2015.1005032
Cheng J, Cheng SH (2012) Influence of carbon nanotube length on toxicity to zebrafish embryos.
Int J Nanomedicine 7:3731–3739. https://doi.org/10.2147/IJN.S30459
Cheng J, Flahaut E, Cheng SH (2007) Effect of carbon nanotubes on developing zebrafish (Danio
rerio) embryos. Environ Toxicol Chem 26(4):708–716. https://doi.org/10.1897/06- 272r.1
Cheng J, Chan CM, Veca LM, Poon WL, Chan PK, Qu L, Sun YP, Cheng SH (2009) Acute and
long-term effects after single loading of functionalized multi-walled carbon nanotubes into
zebrafish (Danio rerio). Toxicol Appl Pharmacol 235(2):216–225. https://doi.org/10.1016/j.
taap.2008.12.006
Chilvers RA, Bodenburg YH, Denner LA, Urban RJ (2012) Development of a novel protocol for
isolation and purification of human granulosa cells. J Assist Reprod Genet 29(6):547–556.
https://doi.org/10.1007/s10815- 012- 9739- 5
A. G. Cattaneo
Brannen KC, Chapin RE, Jacobs AC, Green ML (2016) Alternative models of developmental and
reproductive toxicity in pharmaceutical risk assessment and the 3Rs. ILAR J 57(2):144–156.
https://doi.org/10.1093/ilar/ilw026
Braydich-Stolle L, Hussain S, Schlager JJ, Hofmann MC (2005) In vitro cytotoxicity of nanoparticles in mammalian germline stem cells. Toxicol Sci 88(2):412–419. https://doi.org/10.1093/
toxsci/kfi256
Braydich-Stolle LK, Lucas B, Schrand A, Murdock RC, Lee T, Schlager JJ, Hussain SM, Hofmann
MC (2010) Silver nanoparticles disrupt GDNF/Fyn kinase signaling in spermatogonial stem
cells. Toxicol Sci 116(2):577–589. https://doi.org/10.1093/toxsci/kfq148
Busquet F, Strecker R, Rawlings JM, Belanger SE, Braunbeck T, Carr GJ, Cenijn P, Fochtman P,
Gourmelon A, Hübler N, Kleensang A, Knöbel M, Kussatz C, Legler J, Lillicrap A, MartínezJerónimo F, Polleichtner C, Rzodeczko H, Salinas E, Schneider KE, Scholz S, van den
Brandhof EJ, van der Ven LT, Walter-Rohde S, Weigt S, Witters H, Halder M (2014) OECD
validation study to assess intra- and inter-laboratory reproducibility of the zebrafish embryo
toxicity test for acute aquatic toxicity testing. Regul Toxicol Pharmacol 69(3):496–511. https://
doi.org/10.1016/j.yrtph.2014.05.018
Caldeira DF, Paulini F, Silva RC, Azevedo RB, Lucci CM (2017) In vitro exposure of bull sperm
cells to DMSA-coated maghemite nanoparticles does not affect cell functionality or structure.
Int J Hyperth 34(4):415–422. https://doi.org/10.1080/02656736.2017.1341646
Calienni MN, Feas DA, Igartúa DE, Chiaramoni NS, Alonso SDV, Prieto MJ (2017)
Nanotoxicological and teratogenic effects: a linkage between dendrimer surface charge and
zebrafish developmental stages. Toxicol Appl Pharmacol 337:1–11. https://doi.org/10.1016/j.
taap.2017.10.003
Campos VF, de Leon PM, Komninou ER, Dellagostin OA, Deschamps JC, Seixas FK, Collares T
(2011) NanoSMGT: transgene transmission into bovine embryos using halloysite clay nanotubes or nanopolymer to improve transfection efficiency. Theriogenology 76(8):1552–1560.
https://doi.org/10.1016/j.theriogenology.2011.06.027
Cartwright L, Poulsen MS, Nielsen HM, Pojana G, Knudsen LE, Saunders M, Rytting E (2012)
In vitro placental model optimization for nanoparticle transport studies. Int J Nanomedicine
7:497–510. https://doi.org/10.2147/IJN.S26601
Cattaneo AG (2018) Nanotoxicological evaluation in marine water ecosystem: a detailed review.
In: Kumar V, Dasgupta N, Ranjan S (eds) Environmental toxicity of nanomaterials. CRC Press,
Taylor and Francis Group, Boca Raton, USA. Chapter 3, pp 47–76
Celá P, Veselá B, Matalová E, Večeřa Z, Buchtová M (2014) Embryonic toxicity of nanoparticles.
Cells Tissues Organs 199(1):1–23. https://doi.org/10.1159/000362163
Chan W-H, Shiao N-H (2008) Cytotoxic effect of CdSe quantum dots on mouse embryonic development. Acta Pharmacol Sin 28(2):259–266. https://doi.org/10.1111/j.1745- 7254.2008.00743.x
Chen L, Qiu R, Li L (2014) The role of nanotechnology in induced pluripotent and embryonic stem
cell research. J Biomed Nanotechnol 10:3431–3461. https://doi.org/10.1166/jbn.2014.2043
Chen Y, Hu X, Sun J, Zhou Q (2015) Specific nanotoxicity of graphene oxide during zebrafish embryogenesis. Nanotoxicology 10(1):42–52. https://doi.org/10.3109/1743539
0.2015.1005032
Cheng J, Cheng SH (2012) Influence of carbon nanotube length on toxicity to zebrafish embryos.
Int J Nanomedicine 7:3731–3739. https://doi.org/10.2147/IJN.S30459
Cheng J, Flahaut E, Cheng SH (2007) Effect of carbon nanotubes on developing zebrafish (Danio
rerio) embryos. Environ Toxicol Chem 26(4):708–716. https://doi.org/10.1897/06- 272r.1
Cheng J, Chan CM, Veca LM, Poon WL, Chan PK, Qu L, Sun YP, Cheng SH (2009) Acute and
long-term effects after single loading of functionalized multi-walled carbon nanotubes into
zebrafish (Danio rerio). Toxicol Appl Pharmacol 235(2):216–225. https://doi.org/10.1016/j.
taap.2008.12.006
Chilvers RA, Bodenburg YH, Denner LA, Urban RJ (2012) Development of a novel protocol for
isolation and purification of human granulosa cells. J Assist Reprod Genet 29(6):547–556.
https://doi.org/10.1007/s10815- 012- 9739- 5
A. G. Cattaneo