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 | 8Â mg/kg | 8Â days | Enhance the hyperthermia efficacy | [12] |
Citrate | Citrate@IONPs | Elderly and young healthy mice | 2.4Â mg Fe/kg | 28Â days | Reasonably biocompatible for young mice | [16] |
Polyethylene glycol | SaNPs | Swine | 22Â mg IO/kg, 3.6Â mg IO/kg | 90Â 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 | 30Â mg Fe/kg | 8Â days | Tumors on mice were obviously inhibited | [42] |
Macrophage membranes | Fe3O4@MM NPs | BALB/c mice | 2.5Â mg Fe/kg | 16Â days | Significantly reduce the tumor size | [43] |
Dopamine sulfonate, zwitterionic dopamine sulfonate, coryneine chloride | FeOx NPs | CD1 mice | 1 or 4Â mg Fe/kg | Â | Rapidly distributed in liver and spleen, and excreted via urinary system | [44] |
/ | Fe3O4 NPs | Swiss mice | 1, 2Â mg Fe/kg | 12, 22Â 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 | 20Â mg Fe/kg | 24Â h | Mainly uptake by liver, besides spleen, heart and kidneys | [49] |
Citrate, curcumin, chitosan | IONPs@citrate, IONPs@curcumin, IONPs@chitosan | Wistar rats | 4Â mg Fe/kg | 10Â days | IONPs@curcumin and IONPs@chitosan were mild toxic | [50] |
Chloride, lactate, nitrate | IONPs@chloride, IONPs@lactate, and IONPs@nitrate | Wistar rats | 100Â mg/kg | 14Â days | No signs of toxicity | [51] |
Human albumin | IONPs@human albumin | Wistar rats | 2Â mg Fe/kg | 24Â h | Firstly gathered in liver, then in spleen and kidney | [52] |
Dimercaptosuccinic acid | IONPs@DMSA | C57BL/6 mice | 15Â mg Fe/kg | 7, 30, 60, 90Â days | No toxicity | [53] |
/ | ES-IONPs | U-87 MG tumor-bearing nude mice | 5Â mg Fe/kg | 28Â days | Accumulate in tumor | [54] |
Poly (ethylene glycol) carboxyl-poly(É›-caprolactone) | PEG-PCCL-IONPs | H22 tumor xenograft BALB/c mice | 20Â mg/kg | 48Â h | Mainly distributed in the spleen and liver | [55] |
Dextran | SPIONdex | Pig model | 5Â mg Fe/kg | 30Â min | No complement activation-related pseudoallergy observed | [56] |
Lactobionic acid | MNP-LBA | Albino rabbit | 25, 50Â mg/kg | 24Â h | Enhance the release of ceftriaxone | [57] |
Polyethylene glycol-COOH, Polyethylene glycol-NH2 | SPION@PEG-COOH and SPION@PEG-NH2 | BALB/c mice | 0.8Â mM Fe/kg | 28Â 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 | 0.1Â mg Fe/kg | 7Â days | Increase the adipose tissue in the inferior layer of the epidermis of mice | [61] |
Poly(lactide) | PLA@SPIONs | Sprague Dawley rats | 2 cm2 | 6Â 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 | 10Â mg/kg | 7Â 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 | 100Â mg/kg | 7Â days | No significantly toxicity | [67] |
Glypican-3-specific aptamer | Apt-USPIO | Kunming mice | 1Â mg Fe/mL | 30Â days | Excellent biocompatible | [68] |