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Table 1 Summary of different types of iron oxide nanoparticles (IONPs) in animal models

From: Recent trends in preparation and biomedical applications of iron oxide nanoparticles

Coating molecule

Name

Model

Dose

Days

Outcome

References

Polyethylene glycol

PEG-MGNCs

SCC7 tumor-bearing mouse

8 mg/kg

8 days

Enhance the hyperthermia efficacy

[12]

Citrate

Citrate@IONPs

Elderly and young healthy mice

2.4 mg Fe/kg

28 days

Reasonably biocompatible for young mice

[16]

Polyethylene glycol

SaNPs

Swine

22 mg IO/kg, 3.6 mg IO/kg

90 days

No adverse effects

[40]

Chitosan

γ-Fe2O3/PLGA/CS NPs, γ-Fe2O3/PLGA NPs

BALB/c mice

5 mg/kg

1, 24 h

No toxicity in vital organs

[41]

c(RGDyK)and D-glucosamine

Fe3O4@RGD@GLU

BALB/c mice

30 mg Fe/kg

8 days

Tumors on mice were obviously inhibited

[42]

Macrophage membranes

Fe3O4@MM NPs

BALB/c mice

2.5 mg Fe/kg

16 days

Significantly reduce the tumor size

[43]

Dopamine sulfonate, zwitterionic dopamine sulfonate, coryneine chloride

FeOx NPs

CD1 mice

1 or 4 mg Fe/kg

 

Rapidly distributed in liver and spleen, and excreted via urinary system

[44]

/

Fe3O4 NPs

Swiss mice

1, 2 mg Fe/kg

12, 22 days

Significantly reduce the tumor growth

[45]

6 − 7 bovine serum albumin

Fe2O3@BSA

SD rats

0.15 mM Fe/kg

24, 48 h

Efficiently cleared within 48 h

[46]

Poly (ethylene glycol)-L-arginine

PEG-Arg@IONPs

BALB/c mice

20 mg Fe/kg

24 h

Mainly uptake by liver, besides spleen, heart and kidneys

[49]

Citrate, curcumin, chitosan

IONPs@citrate, IONPs@curcumin, IONPs@chitosan

Wistar rats

4 mg Fe/kg

10 days

IONPs@curcumin and IONPs@chitosan were mild toxic

[50]

Chloride, lactate, nitrate

IONPs@chloride, IONPs@lactate, and IONPs@nitrate

Wistar rats

100 mg/kg

14 days

No signs of toxicity

[51]

Human albumin

IONPs@human albumin

Wistar rats

2 mg Fe/kg

24 h

Firstly gathered in liver, then in spleen and kidney

[52]

Dimercaptosuccinic acid

IONPs@DMSA

C57BL/6 mice

15 mg Fe/kg

7, 30, 60, 90 days

No toxicity

[53]

/

ES-IONPs

U-87 MG tumor-bearing nude mice

5 mg Fe/kg

28 days

Accumulate in tumor

[54]

Poly (ethylene glycol) carboxyl-poly(É›-caprolactone)

PEG-PCCL-IONPs

H22 tumor xenograft BALB/c mice

20 mg/kg

48 h

Mainly distributed in the spleen and liver

[55]

Dextran

SPIONdex

Pig model

5 mg Fe/kg

30 min

No complement activation-related pseudoallergy observed

[56]

Lactobionic acid

MNP-LBA

Albino rabbit

25, 50 mg/kg

24 h

Enhance the release of ceftriaxone

[57]

Polyethylene glycol-COOH, Polyethylene glycol-NH2

SPION@PEG-COOH and SPION@PEG-NH2

BALB/c mice

0.8 mM Fe/kg

28 days

Mainly accumulated in the lung

[58]

Polyethylene glycol

PEG·SPIONs

Kunming mice

2.5 mg Fe/kg

14 days

Primarily in the liver, spleen, and intestine,

[59]

Didodecyl-dimethyl-ammonium-bromide, tocopheryl-polyetheleneglycol-succinate

SPION-DMAB, SPION-TPGS

Swiss albino mice

12.5 μg Fe/kg

7 days

SPION-DMAB mainly accumulated in brain and spleen, while SPION-TPGS internalized in liver and kidney

[60]

L-cysteine

Cys-Fe3O4 NPs

BALB/c mice

0.1 mg Fe/kg

7 days

Increase the adipose tissue in the inferior layer of the epidermis of mice

[61]

Poly(lactide)

PLA@SPIONs

Sprague Dawley rats

2 cm2

6 months

Slow degradation

[62]

Oleic acid and methoxy-polyethylene glycol-phospholipid

SPION-PEG2000

Swiss albino mice

12.5–50 mg/kg

14 days

Induced necrosis in liver and kidney and inflammatory infiltration in lung

[63]

Silica

sub-5 SIO-Fl

CD-1 mice

10 mg/kg

7 weeks

No obviously acute and chronic toxicity

[64]

/

SPION

Sprague Dawley rats

10–40 μg/mL

8 weeks

Enhanced the formation of chondrogenesis

[65]

Galactomannan

PSP-IO NPs

BALB/c mice

10–50 mg/kg

14 days

Increased the accumulation of methotrexate in the tumor site and decrease the toxicity of methotrexate

[66]

/

USPIONs

ICR mice

100 mg/kg

7 days

No significantly toxicity

[67]

Glypican-3-specific aptamer

Apt-USPIO

Kunming mice

1 mg Fe/mL

30 days

Excellent biocompatible

[68]