Compare study | Animal species | Â Size, nm | Modification | Dose | Exposed time, d | Effects | LD50 | Ref |
---|---|---|---|---|---|---|---|---|
 | Mice | 35 |  | 0.1 mg Se/kg diet | 45 | SeNPs-M showed↑ Se retention and the levels of glutathione peroxidase, superoxide dismutase and catalase | 72 mg/kg | [45] |
 | Mice | 20 |  | 200 μg Se/kg BW/d | 90 | Under the safe dose (0.75–7.5 mg/kg), oral administration of PTR-SeNPs dramatically inhibited the growth of cancer in a tumor-bearing nude mouse mode | 20 mg/kg | [46] |
 | Mice | 40–55 |  | 2 mg Se/kg BW/d | 28 | SeNPs, caused↓ bone marrow cell death and prevented DNA damage, compared to other forms of selenium |  | [47] |
 | Mice | 20 |  | 0.5, 5, and 50 mg Se/kg diet | 14 | Toxicity ↑ when inorganic Se was applied than after subacute application of Sel-Plex, nanoSe, or LactoMicroSe |  | [48] |
 | Mice | 70–90 |  | 1 and 4 mg Se/kg | 28 | Nano-selenium at low dose (1 mg/kg) exhibited antioxidant effects in the liver compared to the high dose (4 mg/kg) of SeNPs and sodium selenite (1 and 4 mg/kg) | 113.87 mg/kg | [49] |
 | Mice | 50 | Chitosan | 10.5 g Se/kg | 45 | Acute fetal test showed SeNPs-C/C was safer than selenite, with a median lethal dose (LD50) of approximately 4-fold to 11-fold of that of selenite | 8.8 mg/kg | [50] |
Na2SeO3 | Mice | 5 |  | 2, 4 and 6 mg/kg BW | 15 | Selenite and SeNPs completely and partially suppressed mice growth respectively. Abnormal liver function was more pronounced with selenite treatment than SeNPs | 15.7 mg/kg | [51] |
SeMetCys | Mice | 20–60 |  | 10 mg Se/kg | 7 | ↓Body growth, ireversible changes by SeMSC, reversible changes by SeNPs in liver; ↑ serum ALT and LDH in SeMSC compared to SeNPs and ctrl. ↑ GST activity in SeNPs group compared to SeMSC and ctrl; ↓ T-AOC in SeMSC group, not in SeNPs group | SeMSC 14.6 mg Se/kg and SeNPs 92.1 mg Se/kg | [39] |
SeMet | Mice | 20–60 |  | 10 mg Se/kg | 7 | ↑Gpx and thioredoxin reductase, ↓toxicity as indicated by median lethal dose, acute liver injury, and short-term toxicity by SeNPs | 27.0 mg/kg | [52] |
SeO2 | Mice | 80–220 | Green synthetized via Bacillus sp. | 2.5, 5, 10, 20 mg/kg BW | 14 | ↓ Body weight, ↑ AST, ALT, ALP, Cr, Chol, TG, TB and worsed hematological parameters in total blood at the dose of 20 mg/kg | SeO2–7.3 mg/kg SeNPs 198.1 mg/kg | [53] |
 | Rats | 78.88 |  | 2, 4, and 8 mg Se/kg BW | 14 | ↓ Antioxidant capacity in serum, liver, heart; ↓ expression of GPx-1 and GPx-4 in liver; ↑MDA in liver |  | [54] |
 | Rats | 79.88 |  | 0.2, 0.4, 0.8, 2.0, 4.0, or 8.0 mg Se/kg BW | 14 | ↓ Body weight, ↑ ALP, SAST, CHol, ↑ liver weight; ↓ thymus weight; ↑ Apoptotic cells count in liver |  | [37] |
 | Rats | 4.6, 24.5 | κ-carrageenan-capped SeNPs | 500 μg/kg BW | 10 | ↓ Count of astroglial cells in brain; ↑ Se accumulation in liver, kidneys, brain in 4.6 nm SeNPs treated group; − changes in internal organs and glands |  | [37] |
Na2SeO3 | Rats | 100–150 | Green synthetized via potatoe extract, PEG coated | 5, 10, 15 μg/kg | 21 | Organ weight in SeNPs groups; ↓ decreased weight of internal organs in sodium selenite group; no differences in heamatological parameters in sodium selenite group X markable changes in SeNPs group compared to ctrl; sodium selenite negatively affected; histopathology of liver, but not SeNPs; ↓ concentration of Se in breast milk in SeNPs compared to sodium selenite and ctrl group |  | [55] |
Na2SeO3 | Rats | 20 |  | 0.05, 0.5, or 4 mg Se/kg BW | 28 | ↓ Body weight; − neurotransmitters, hematological parameters, histology of liver |  | [35] |
Na2SeO3 | Rats | 80 | PVA modified | 1.2 mg Se/kg | 30 | ↓ GSH in liver for Se, SeNPs groups; ↑ GSSG in liver for Se, SeNPs groups; higher retention of Se in group of SeNPs compared to Se group in blood |  | [56] |
 | Rats | 79.88 |  | 0.2, 0.4, 0.8 mg Se/kg BW | 14 | The supranutritional ↑ sperm motility and movement parameters, The nonlethal levels of 4.0 and 8.0 mg Se/kg BW ↓ testisweight, sperm concentration, and motility and also caused histopathological injury of testisand epididymis tissues to various degrees |  | [57] |
 | Rats | 100 |  | 0.5, 1.5, 3.0 and 5.0 mg Se/kg | 28 | Histopathological examination showed damage to the liver parenchyma and intestinal epithelium, ↓ ALT activity | 7 mg/kg | [58] |
Na2SeO3 | Rats |  |  | 10, 18 mg/kg | 10 | CK, CK-MB and LDH levels of Group IV ↑ other groups on both the 2nd and 10th days. In Groups II and III, this serum level decreased, and vitamin B12 ↑ | 10 mg/kg | [59] |
 | Rats | 5–100 |  | 2, 3, 4 and 5 ppm | 91 | The toxicity was ↑more pronounced in the selenite and high-selenium protein groups than the Nano-Se group | 113 mg/kg | [60] |
Na2SeO3 | Rats | 20–60 |  | 0.0096 and 0.1 ppm | 14 | SeNPs has a 7-fold lower acute toxicity than sodium selenite in mice (LD50 113 and 15 mg Se/kg body weight respectively | 15.7 mg/kg | [61] |
Na2SeO3 | Rabbits |  |  | 0.3 mg/kg BW | 42 | − Chol, TG, TP, Glu, ALT, AST, ↑ GPx mRNA expression, TAOC |  |  |
Na2SeO3 | Chickens | 100 | Green synthetized | 0.3 mg Se/kg diet | 42 | − Serum glucose, cholesterol, lipoprotein, thyroid hormone, and liver function levels and biomarkers of kidney function; ↓ lowest relative weight of the liver; ↑ otal protein in serum |  | [62] |
 | Chickens | 60 |  | 0.15, 0.30, 0.60 and 1.20 mg/kg/d | 49 | Se in serum, liver and breast muscle ↑, magnitude of increase was substantially ↑ when Nano Se was fed | 113.0 mg/kg | [63] |
SeYeast, SeMet | Chickens |  |  | 0.1 and 0.3 mg/kg diet | 42 | SeNPs improved yellowness, redness and meat quality, NS and organic sources of Se resulted in better meat quality |  | [64] |
 | Chickens | 100 |  | 0.3, 0.9 and 1.5 ppm | 29 | inorganic Se caused↓bioavailability in breast and duodenum tissue and↑ accumulation in organs involved in detoxification compared to organic selenium SeNPs |  | [65] |
 | Chickens | 200 |  | 0.15, 0.30, 0.45 ppm | 32 | SeHME showed ↑ expression of GPx-4 in the livers and SelW in the spleens compared with SeS treatment |  | [66] |
 | Chickens | 100 |  | 0.3, 0.9 and 1.5 ppm | 29 | Inorganic Se leads↓ bioavailability in breast and duodenum tissue and ↑ accumulation in organs involved in detoxification processes as compared to organic Se and SeNPs |  | [65] |
 | Sheeps | 40 |  | 5 mg Se/kg BW | 30 | HB, RBCs, and PCV in Nano-Se ↓, SLD, GOT, CTT and AP in Nano-Se group was↑. Levels of IgG, IgM, IgA, IL-2,TNF-α in NanoSe group were↓ than those of the control. |  | [67] |
SeMet, Na2SeO3 | Piglets | 28–59 |  | 0.3 mg Se/kg diet | 28 | ↑ Glutathion peroxidasis, expression of selenoprotein W (SELW), GPx1, and GPx3 in the liver |  | [68] |
 | Pigs | 100 |  | 0.5 mg Se/kg diet | 45 | − Performance; ↑ concentration Se in muscle, T-AOC, GPx, SOD, CAT; ↓ MDA |  | [69] |
SeYeast | Sheep |  |  | 4 mg/kg | 25 | Ruminal pH, ammonia N concentration, molar proportion of propionate, ratio of acetate to propionate ↓and total ruminal VFA concentration was ↑ with NS and YS |  | [70] |
Na2SeO3 | Cows | 100 |  | 0.3 mg Se/kg diet | 30 | −Matter intake, milk yield and composition; ↑ plasma Se levels and GPx; ↓ mRNA expression levels of glutathione peroxidase 1, 2 and 4; thioredoxin reductase 2 and 3; and selenoproteins W, T, K and F |  | [71] |