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. 2022 Jun 15;4:895667. doi: 10.3389/ftox.2022.895667

TABLE 1.

Adverse effects and toxicological implications of various types of nanoparticles in the female reproductive system and stages of fetal development.

Type of NPs Size/size range Dose/concentration Animals/model Toxicological outcomes Reference
Polyvinyl pyrrolidone–coated silver NPs 20–50 nm 0.427, 0.407, and 0.013 mg/kg Rats NPs are causing impairing of cognition in the offspring. Wu et al. (2015)
Gold NPs 10 2.85 × 1010 NPs/ml In vitro NPs are found to be affecting steroidogenetic capacities by the granulosa cells in culture media after trespassing through the granulosa cell membranes. Lyngdoh et al. (2020)
Silver nanoparticles 14 nm 50 nM Mice Inner cellular mass was subjected to the induced apoptosis, and embryonic growth shows trophectoderm. Li et al. (2010)
Gold NPs 13 0.9–7.2 μg/g body weight Mice NPs get accumulated in the placental and fetal tissues. Yang et al. (2018); Bongaerts et al. (2020)
Silver nanoparticles 35 nm 1.69–2.21 mg/kg Rats NPs show appearance in the fetal growth. Melnik et al. (2013)
Gold NPs 20 1 nm for 48 or 72 h In-vitro NPs cause the alteration of almost 19 genetic makeups in the fibroblast cells of the lungs of the fetus. Gedda et al. (2019)
Silver nanoparticles 8 nm 250 mg/kg Rats Pups’ tissues exhibit NP accumulation. Lee et al. (2012)
Gold NPs 20 & 50 0.01% Mice NPs can travel through the placenta through endocytic vesicular transportation Rattanapinyopituk et al. (2014)
Silver nanoparticles 0.001–100 μg/ml In vitro NPs show interference in the reproductive tissue function and alter levels of E2 and P4. Scsukova et al. (2013)
Gold NPs 3, 13 & 32 nm 0.9 μg/g body weight Mice NPs are found to be enhancing the inflammation of uterine tissues and get accumulated in fetal tissues Tian et al. (2013)
Silver nanoparticles 0.09–1.0 mg/ml In vitro Intervention by NPs in proliferative pathways and cause apoptotic implications in granulosa cell lines of pork ovaries Kolesarova et al. (2011)
Gold, silver, and gold-silver alloy 6 and 20 nm 0.66 g/L for alloy, 2.5 g/L for silver, and 0.5 g/L for gold Pigs’ in vitro ovaries NPs are found to be inhibiting the maturation of oocytes, and toxic impacts are increased by the NPs of alloys. Tiedemann et al. (2014)
Silver nanoparticles 35 nm 1.69–2.21 mg/kg Mice NPs travel in the mother’s breast milk and get accumulated in the developing embryos Melnik et al. (2013)
Titanium dioxide NPs 5.5 nm 10 mg/kg Mice Initiation of premature oogenesis and causing the apoptotic cell death in ovarian cells, enhancing the atresia in primary and secondary follicular developmental stages Zhao et al. (2013)
Silver nanoparticles 55 nm 0.2–20 mg/kg Rats Nanoparticle demons Charehsaz et al. (2016)
Titanium dioxide NPs 25 nm -- In vitro Deformation of follicular growth and inhibition of the maturation of oocytes Hou and Zhu, (2017)
Silver nitrate NPs 55 nm 20 mg/kg Rats NPs damage neurons in the hippocampal regions of the brains of both adults and offspring. Charehsaz et al. (2016)
Titanium dioxide NPs 13–27 nm 1–5 μg/ml Chinese hamster ovary cell line Genotoxic and cytotoxic outcomes Kazimirova et al. (2020)
Cadmium oxide NPs 11–15 nm 100 or 230 µg Mice Placental toxic reactions Blum et al. (2012)
Silver or silver nitrate NPs 10 nm 66 mg/kg Mice NPs caused hampering of the growth of embryos Austin et al. (2016)
Titanium dioxide NPs -- 2.5, 5, and 10 mg/kg body weight Mice Alteration in the expressions of relevant ovarian genes in a concentration-dependent manner Zhao et al. (2013)
Titanium dioxide NPs -- 0.001–100 μg/ml In vitro Alteration in the levels of P4 and E2 and interference in reproductive system functions Karimipour et al. (2018)
Titanium dioxide NPs 50 nm 1 μg/ml Mice NPs crossed the placental barrier and hampered the central nervous system development in the fetus Shimizu et al. (2009); Umezawa et al. (2012)
Titanium dioxide NPs 10 nm 100 mg/kg body weight Rats NPs exerted neurotoxicity in the brains of neonates and adults Mohammadipour et al. (2014), Mohammadipour et al. (2016); Ebrahimzadeh Bideskan et al. (2017)
Titanium dioxide NPs ∼100 nm 100 mg/kg body weight Rats Induction of apoptotic phenomena and reduction in neurogenesis Mohammadipour et al. (2014), Mohammadipour et al. (2016); Ebrahimzadeh Bideskan et al. (2017)
Titanium dioxide NPs 35 nm 0.8 mg per animal Mice Accumulation of NPs in the brain, placental trophoblasts, and liver of the fetus Yamashita et al. (2011)
Titanium dioxide NPs 4 nm 88–108 m2/gm Ex-vivo Placental toxicities Blum et al. (2012)
Aluminum oxide NPs 9–47 nm 1–25 μg/ml Chinese hamster ovary cell line Cytotoxic and genotoxic effects Di Virgilio et al. (2010)
Cerium oxide NPs 35 nm 100 µm Mice Adverse reactions on oocytes Courbiere et al. (2013)
Cerium oxide NPs 35 nm 10 & 100 µm Mice NPs got aggregated and accumulated in follicular cells by the endocytotic mechanism and showed distribution in zona pellucida of oocyte cells Preaubert et al. (2016)
Zinc oxide NPs ∼100 nm 500 mg/kg Rats Reduction in the numbers of live-born pups and enhancement of fetal repsorptive phenomena Jo et al. (2013)
Zinc oxide NPs ∼20 nm 50 or 100 mg/kg Hens Inflammatory responses, ROS production, and disturbances in the signaling pathway Liu et al. (2016)
Polyethylene imine and PAA-coated iron oxide NPs 28–30 nm 50 mg/kg body weight Mice NPs lead to the death of the fetus. Di Bona et al. (2014)
Alpha-iron oxide NPs 50 & 70 nm 100 μg/ml In vitro Oxidative stress and cellular death Faust et al. (2014)
Cadmium oxide NPs 11–15 nm 100 and 230 mg/m3 Mice NPs show accumulation in placental tissues and an increase in the weight of the fetus. Liu et al. (2017)
Silver NPs 5–70 nm 0.2 & 2 mg/kg Mice NPs caused neurobehavioral impairments in the offspring. Ghaderi et al. (2015)
Copper oxide NPs 4 nm 40–44 m2/g Ex vivo Reduced cell viabilities and reduction in levels of human chorionic gonadotropins Blum et al. (2012)