Biodistribution, pharmacokinetics, and toxicity of dendrimer-coated iron oxide nanoparticles in BALB/c mice
Authors Salimi M, Sarkar S, Fathi S, Alizadeh AM, Saber R, Moradi F, Delavari H
Received 16 November 2017
Accepted for publication 6 February 2018
Published 13 March 2018 Volume 2018:13 Pages 1483—1493
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Prof. Dr. Thomas J. Webster
Marzieh Salimi,1,2 Saeed Sarkar,1,2 Samaneh Fathi,3 Ali Mohammad Alizadeh,4 Reza Saber,2,3 Fatemeh Moradi,5 Hamid Delavari6
1Department of Medical Physics and Biomedical Engineering, Tehran University of Medical Sciences, Tehran, Iran; 2Research Center of Science and Technology in Medicine, Tehran University of Medical Sciences, Tehran, Iran; 3Department of Medical Nanotechnology, Tehran University of Medical Sciences, Tehran, Iran; 4Cancer Research Center, Tehran University of Medical Sciences, Tehran, Iran; 5Department of Medical Physiology, Tehran University of Medical Sciences, Tehran, Iran; 6Department of Materials Science and Engineering, Tarbiat Modares University, Tehran, Iran
Background: The possibility of using a specific nanoparticle in nanomedicine highly depends on its biodistribution profile and biocompatibility. Due to growing demand for iron oxide nanoparticles (IONPs) and dendrimers in biomedical applications, this study was performed to assess the biodistribution, pharmacokinetics, and toxicity of dendrimer-coated iron oxide nanoparticles (G4@IONPs).
Materials and methods: IONPs were synthesized via co-precipitation and coated with the fourth generation (G4) of polyamidoamine (PAMAM) dendrimer. To determine the biodistribution, 5 mg/mL G4@IONPs suspension was intraperitoneally injected into tumor-bearing BALB/c mice, and iron levels in blood and various organs, including the lung, liver, brain, heart, tumor, and kidney, were measured by inductively coupled plasma mass spectrometry (ICP-MS) at 4, 8, 12, and 24 h after injection. Also, to investigate the toxicity of G4@IONPs, different concentrations of G4@IONPs were injected into BALB/c mice, and blood, renal, and hepatic factors were measured. Furthermore, histopathological staining was performed to investigate the effect of G4@IONPs on the liver and kidney tissues.
Results: The results showed that the iron content was higher in the kidney, liver, and lung tissues 24 h after injection. Toxicity assessments revealed a significant increase in blood urea nitrogen (BUN) and direct bilirubin at the concentration of 10 mg/kg. Also, in this concentration, histopathological abnormalities were detected in liver tissue.
Conclusion: Although more systematic studies are still required, our results encouraged the future investigations of G4@IONPs in biomedical applications.
Keywords: G4@IONPs, biodistribution, pharmacokinetics, toxicity
Application of nanotechnology in medicine and drug delivery is spreading fast.1 Iron oxide nanoparticles (IONPs) are gradually being studied in different biomedical applications, including magnetic hyperthermia, targeted drug delivery, and magnetic resonance imaging (MRI) contrast agent; therefore, a comprehensive elucidation of their metabolic pathways and clearance mechanisms seems to be essential.2 Particle size, surface charge, and coating are crucial factors affecting the biodistribution, pharmacokinetics, and also toxicity platform of IONPs.3–5
Weissleder et al6 studied the biodistribution of dextran-coated superparamagnetic IONPs with an overall size of 21 nm in the rat; 25% of injected dose per gram tissue (ID/g) localized in the liver 24 h after intravenous injection, while the uptake of 80 nm IONPs in the liver was up to 83% ID only after 1 h. Furthermore, Chouly et al3 showed similar results for biodistribution of dextran-coated IONPs with a range size of 33–90 nm. In this study, the uptake of larger nanoparticles was higher in the liver.
Surface charge is another crucial factor to determine the mechanism of cellular uptake, and the in vivo fate of nanoparticles (NPs).7–9 Papisov et al10 compared the positively charged and negatively charged dextran-coated IONPs biodistribution with a size of 26 nm in rats. The results clearly demonstrated that positively charged NPs mainly accumulated in the liver and spleen with a faster clearance (2 min), while the negatively charged ones were detected in the lymph nodes with a long clearance (50 min). On the other hand, the neutral surface charged IONPs had the longest circulation time, and also their uptake in the liver and spleen was much lower than positively and negatively charged ones.3 In another study, Xiao et al11 assessed the effect of surface charge on biodistribution of PEG-oligocholic acid based micellar NPs. The results clearly showed a high liver uptake for high positively or negatively charged NPs, while slightly negative particles had a very low liver uptake.
The coating of IONPs decreases their uptake in reticuloendothelial system (RES) organs, and makes the blood circulation time longer, which is important in biomedical applications including therapy, drug delivery, and imaging.4 Jain et al12 evaluated the biodistribution of 193 nm Pluronic-OA-IONPs; 55% of ID accumulated in the liver 6 h after injection, while the uptake of dextran-coated IONPs was much more in RES (>75%). In another study, IONPs with crosslinked starch and PEG coating exhibited increased half-life circulation (7–12 h).13
Another material which is used for surface coating of IONPs is dendrimer, which has attracted considerable attention due to its unique physicochemical properties.14 However, the feasibility of using a special coating in biomedical applications highly depends on its biodistribution profile. Opina et al15 investigated the gadolinium (Gd)-labeled G5 PAMAM dendrimers (G5–Gd-BnDOTA) as lymphatic imaging agents, and studied their long-term biodistribution (90-day) in mice.15 The authors concluded that G5–Gd-BnDOTA was an appropriate agent for lymphatic imaging, but its slow clearance might prevent its subsequent clinical applications.
Few studies have investigated the biodistribution and toxicity profile of IONPs with different coatings4,5 and dendrimers in particular. Systematic toxicity studies are required when different types of molecules or polymers are integrated into the coating layer of the IONPs.16 Therefore, we studied the biodistribution, pharmacokinetics, and toxicity of G4@IONPs in BALB/c mice.
Materials and methods
Ferric chloride hexahydrate (FeCl3·6H2O, 99% w/w), ferric sulfate heptahydrate (FeSO4·7H2O, 99% w/w), ammonia solution (NH3, 32% v/v), hydrochloric acid (HCl, 32% v/v), 3-aminopropyltrimethoxysaline (NH2(CH2)3-Si-(OCH3)3, APTS), methanol (99.9% v/v), ethanol (99.9% v/v), methyl acrylate (99.5% v/v), methoxy-PEG, and ethylenediamine (99% v/v) were used in the synthesis process; all materials were purchased from Sigma Aldrich (Hamburg, Germany).
Synthesis of IONPs
IONPs were prepared with the co-precipitation method. First, 0.84 g of FeSO4 and 1.22 g of FeCl3 were dissolved in 20 mL deionized water followed by 30 min sonication. Then, 1 mL of 2M HCl was slowly added with vigorous stirring in a nitrogen atmosphere. After 2 min, 4.6 mL ammonia was quickly added to the solution and stirring was continued for 1 min. The black precipitate of IONPs was washed five times with distilled water and ethanol through magnetic decantation.
Preparation of APTS-coated IONPs
First, 150 mL ethanol was added to 25 mL IONPs with a concentration of 5 g/L. Then, the solution was sonicated for 30 min, and 300 μL of APTS was added to the mixture after 20 min of sonication. The final solution was stirred for 15 h at room temperature and, eventually, the resultant black precipitate was washed with ethanol three times. The obtained materials were G0 dendrimer coated IONPs (G0@IONPs).17
Surface coating with PAMAM dendrimer
First, 10 mL ethanol was added to the G0@IONPs after 30 min sonication; subsequently, methyl acrylate/methanol solution (20%, v/v) was added (50 mL) at 0°C with sonication for 1 h, followed by stirring for 48 h. After washing with methanol and magnetic decantation, ethylenediamine/methanol (50%, v/v) was added (15 mL), and the solution was sonicated for 3 h at 25°C. This procedure was repeated to complete the desired number of dendrimer generation (G4). The product (G4@IONPs) was washed several times with methanol and water by magnetic decantation or centrifugation.18
PEGylation of G4@IONPs
Surface amino groups of dendrimer molecules were conjugated with mPEG (Mw =4,000 Da).19,20 The mPEG mass was three times more than the mass of iron. The mPEG was dissolved in ethanol and added to the G4@IONPs solution followed by 18 h reflux.
The G4@IONPs size and morphology were assessed by transmission electron microscopy (TEM). The hydrodynamic size and surface potential were measured through dynamic light scattering (DLS) and zeta potential, respectively. Also, the crystalline phase of NPs was confirmed by x-ray diffraction (XRD, λ=0.15406 nm) and the presence of saline and PAMAM bonds on the surface of Fe3O4 was shown through Fourier transform infrared (FTIR) spectroscopy.
The Animal Ethics Committee of Tehran University of Medical Sciences approved all animal experiments (IR.TUMS.REC.28169); Applied Research Ethics National Association guidelines were followed for the welfare of the animals. Male and Female BALB/c mice were purchased from the Animal Center of Pasture Research Center. Six- to eight-week-old male BALB/c mice weighing about 25–30 g were kept in groups of five. The groups were housed in individual cages with unlimited access to water and food. The circadian rhythm was 12 h in the light and 12 h in the dark. Male BALB/c mice were used to fulfill the toxicology studies, and female BALB/c mice were used to perform distribution and pharmacokinetics experiments.
Blood chemistry assessments
The short-term (acute) toxicity of G4@IONPs was investigated after administration by intraperitoneal (IP) injection. Concentrations of 100, 50, 25, and 0 (control) mg/kg were administered, and there was no death or severe physical distress in test groups after injection. The mice were sacrificed 24 h after injection, and blood samples were collected in heparin-coated centrifuge tubes and centrifuged at 1,000 rpm for 2 min to acquire the plasma. Total leukocyte count (WBC), erythrocyte count (RBC), platelets (Plt), hemoglobin (Hgb), and hematocrit (Hct) were detected by an animal blood counter (Celltac; Nihon Kohden, Tokyo, Japan). Plasma alkaline phosphatase (ALP), albumin (ALB), total bilirubin, and direct bilirubin were also measured as liver function indicators (BT 3500; Autoanalyser Model Biotecnica, Rome, Italy). Renal function indicators such as BUN, creatine (Cr), and glucose (Glu) were determined using CCX System (CCX WB; Nova Biomedical, Waltham, MA, USA).21,22
The chronic toxicity procedure was performed similarly to the acute toxicity experiment. Concentrations of 10, 5, 1, 0.5, and 0 (control) mg/kg were injected intraperitoneally for 7 days (2 mL per injection). After the 7th day, the mice were sacrificed, and blood samples were collected to analyze the blood, renal, and hepatic factors.
After the blood was collected, the mice were killed by cervical dislocation. The liver and kidney tissues were isolated by incision immediately after necropsy, fixed in a 10% formalin solution containing neutral phosphate-buffered saline (PBS), and stored at 4°C. The tissues were routinely processed, embedded in paraffin, sectioned at 3–5 mm, and then stained with hematoxylin and eosin (H&E) for microscopic examination.23 Micrographs of the sections were recorded for comparison.
To assess the apoptotic effect of G4@IONPs on cardiac tissue, terminal deoxynucleotidyl transferase-mediated dUTP nick end-labeling (TUNEL) staining was done on 10-μm-thick paraffin-embedded sections by means of the In-Situ Cell Death Detection Kit, POD (Roche Applied Science, Penzberg, Germany). Heart-muscle tissue sections were deparaffinized in xylene, rehydrated, and immersed in 3% hydrogen peroxide to block the endogenous peroxidase activity. After rinsing with PBS, the sections were kept with proteinase K solution at 37°C for 30 min to increase the staining, incubated for 60 min at 37°C with 50 μL of TUNEL reaction mixture, and then incubated for 30 min at 37°C with 50 μL of converter POD. Sections were washed in PBS, and then mounted in medium containing DAPI (4′,6-diamidino-2-phenylindole). Microscopic fields (n=5) were randomly selected and evaluated to calculate the ratio of TUNEL positive to TUNEL negative cells. For the positive control, the sections were incubated in DNase1 solution at 15°C–25°C for 10 min, and, for the negative control, enzyme solution was omitted. Finally, the sections were dehydrated again and cover-slipped as described above, and were analyzed under fluorescent microscopy.24
TUNEL positive cell counting
TUNEL positive cells were counted in six adjacent 100× microscopic fields, from which the number of myocytes and the ratio of apoptotic cells to normal cells were obtained. To validate the automatic counting procedure, the number of TUNEL positive cells was manually counted in five selected fields of view in a random manner under 400× magnification for each animal.
Biokinetics and tissue distribution
To study the kinetics and tissue distribution, the mice were given a 5 mg/mL G4@IONPs suspension via IP injection. This dose was chosen since it was low enough to be acutely nontoxic, based on the observation of the acute toxic effects, and was high enough to allow quantification of iron residue levels in organs of interest at later time points. Blood samples (~1 mL for each mouse) regained from the ocular vein were collected at predetermined time intervals (4, 8, 12, and 24 h post-injection). For the tissue distribution study, tissues (lungs, liver, brain, heart, tumor, and kidneys) were harvested at time points of 4, 8, 12, and 24 h after injection. In this experiment, saline was injected into three mice simultaneously as negative controls. All the blood and tissue samples were stored in a −80°C refrigerator for further analysis.
The iron analysis was based on the quantification of iron in several samples using an inductively coupled plasma-mass spectrometry (ICP-MS) method. Blood and tissue samples were thawed before analysis. About 40–80 mg of each sample was weighed, digested, and analyzed for iron content. In brief, before the elemental analysis, the blood and tissue samples of interest were digested in 5 mL nitric acid (32% v/v) overnight. Then 1 mL hydrogen peroxide (H2O2, 30% v/v, metal oxide semiconductor grade) was added to the solution. The solution (~1 mL) was diluted to a total volume of 2 mL with 2% nitric acid. The detection limit of iron was 0.001 ng/mL. Data are expressed as micrograms per gram (parts per million, ppm) of fresh blood or tissue normalized to the control group. To exclude the existing iron in blood and tissues, three mice were considered as a control group (saline injected). The iron content of blood and tissues of the control group was measured by ICP-MS. Finally, the measured iron content in each group was normalized to the result of the control group.
The statistical analysis was performed by one-way analysis of variance (ANOVA) test. Statistical significance was considered at P<0.05 in all experiments. Results are expressed as the mean ± standard deviation (n=3–5).
Synthesis of G4@IONPs
For applications of IONPs in the nanomedicine, physical and chemical characterizations are needed.25,26 The size of G4@IONPs was 10±4 nm according to the TEM images (Figure 1A). The hydrodynamic size of different generations of PAMAM dendrimer coated IONPs were assessed by DLS, and the results clearly showed that the hydrodynamic size of NPs increased by adding each generation of PAMAM dendrimer (Figure 1B). The surface potential of G4@IONPs measured by zeta potential was +35 mV at pH=7 and 25°C. The hydrodynamic sizes of IONPs coated by G1, G2, G3, G4, G4@PEG, and polydispersity of each generation are given in Table 1.
Table 1 The hydrodynamic size of coated IONPs by G1, G2, G3, G4, and G4@PEG, and their polydispersity percentages
Figure 1 (A) TEM image and size distribution of G4@IONPs. (B) DLS shows size distribution and hydrodynamic size of G1, G2, G3, G4, G4@[email protected], (C) XRD result identified the crystal structure and all diffraction peaks assigned to Fe3O4, and (D) FTIR spectra of IONPs coated by G1, G2, G3, G4, G4@PEG.
Results of XRD indicated that all diffraction peaks could be assigned to Fe3O4 without any impurities. The characteristic XRD pattern did not change by coating the NPs with PAMAM dendrimers (Figure 1C).18 Furthermore, the average diffracting crystallite size of G4@IONPs was calculated using Scherrer’s equation, from the most intense peak (311),26,27
where D is the average crystallite size, λ is the wavelength of the incident X rays (0.154 nm), and θ is the diffraction angle (18.5°), β is the full width at half maximum in radians (0.0145), yielding a particle size of 10.6 nm, which is in close agreement with the size (10.65 nm) observed by TEM.
FTIR results related to G1–G4 generation of dendrimer-modified IONPs are shown in Figure 1D. The presence of the Fe3O4 core could be detected by the strong peaks at 570 cm−1, corresponding to the intrinsic stretching vibration of the metal at the tetrahedral site (Fe tetra–O); the NH2 group vibration is at about 3,410 cm−1.28 Moreover, the broad peak at 3,444 cm−1 shown the bending mode of free NH2 groups existing at APTS.29 The peaks of −CO−NH− bonds were detected at 1,450, 1,490, 1,570, and 1,620 cm−1. The peak at 1,151 cm−1 demonstrated the existence of a C=O bond in ester groups, and the band at 1,480 cm−1 was related to the methylene group.30 Associated with alcohols, O−H bonds were at 3,200–3,600 cm−1. In fact, FTIR spectra were well-matched with the stepwise dendrimer modification procedure.
Toxicity of G4@IONPs
Hematology and blood chemistry assessments were performed to study the toxicity effects of G4@IONPs. In acute toxicity assessment, a significant increase in BUN levels (30 g/dL) and hyperuricemia were detected at 100 mg/kg (P<0.05).
Chronic exposure did not significantly change blood parameters (Figure 2A) and renal function indicators (Figure 2B) at all G4@IONPs concentrations. There was also a non-significant increase in ALP and ALT (alanine aminotransferase) enzymes, possibly due to the transfer of oleic acid molecules from liver macrophages to hepatocytes, or the impact of G4@IONPs injection (Figure 2C). Furthermore, direct bilirubin (an estimate of the conjugated bilirubin) increased significantly (P<0.05) at 10 mg/kg (0.66 g/dL versus 0.2 g/dL in the control group).
Histological analysis of kidney and liver
To obtain an accurate evaluation of G4@IONPs toxicity at the microscopic level, histological staining of kidney and liver tissues was performed (Figure 3). The histopathological results showed edema and losing cytoplasm in the liver cells at 10 mg/kg. There were no significant histopathological variations in the kidney cells in all mice. At doses of 5, 1, and 0.5 mg/kg, no histological abnormalities were detected.
Apoptosis in cardiac tissue
Based on chronic toxicity results, we found out that lactate dehydrogenase (LDH) was elevated at concentrations of 10 and 5 mg/kg. Since this could be a sign of heart injury, TUNEL staining was performed to assess the cardiac toxicity of G4@IONPs more precisely. The outcomes revealed that apoptosis significantly increased at these concentrations (Figure 4A–E). Also, the quantity (%) of apoptotic cells were 73% and 52% at concentrations of 10 and 5 mg/kg, respectively, compared to 21% in the sham group (Figure 4F). The TUNEL results thereby confirmed blood chemistry outcomes.
Biokinetics, tissue distribution, and hemostability of G4@IONPs
Blood concentration of G4@IONPs in different time points after IP injection into mice is shown in Figure 5A. The blood iron levels persisted and increased slightly up to 4 h (2.72 ppm) and then decreased to a lower level of 1.57 ppm until 8 h. Finally, at the end of 24 h, the iron concentration decreased to almost half of the maximum amount detected at 4 h (1.61 ppm). In control mice, 1.2 ppm iron was detected (without any iron injection).
To investigate the tissue distribution and disposition of G4@IONPs, the concentration of iron in lung, liver, brain, heart, tumor, and kidney tissues at 4, 8, 12, and 24 h after IP injection was determined by the ICP-MS method (Figure 5B).
After administration of a single dose of 5 mg/kg, the iron content was higher in the kidney, liver, and lung. The level of iron in the brain remained steady for the entire duration of the experiment (0.45 ppm). In the liver, 1.92 ppm of iron was detected during the first 4 h, then a severe decreasing trend was observed after 8 h (0.84 ppm); finally, 1.27 ppm of iron was detected in the liver, which was almost half of that detected in kidney tissue at this time point (2.47 ppm). It seemed that G4@IONPs due to their minute size were mostly excreted by kidneys and were finally absorbed in lung tissue. In the lung, the results showed a steady state in iron level during the experimental time, with an increase at 24 h (1.92 ppm). Also, in the tumor tissue, iron content decreased with time; after 4 h, 1.07 ppm of iron was detected in this tissue, while it was just 0.75 ppm after 24 h.
Nowadays, dendrimers have attracted a great deal of attention, especially in drug delivery and imaging. It is, therefore, vital to assess their toxicity and biodistribution.20,31–33 In this study, the G4@IONPs were synthesized by co-precipitation and coated with G4 PAMAM dendrimer in a stepwise manner. The results of DLS showed that, by adding each generation of coating layer, the hydrodynamic size of NPs increased. The hydrodynamic diameter was notably larger than the size measured by TEM; that might be due to two main reasons; the scattering of small particles varies strongly with particle radius in DLS, and the signal of larger particles can still overwhelm the signal of smaller ones.
The main disadvantage of DLS is the difficulty in data interpretation of polydispersity with wide particle size distribution. Bigger particles contribute to increasing the light scattering and shifting the measured size toward larger values.34,35 The polydispersity of G4@IONPs as measured by TEM and DLS was approximately 32%. In this situation, the enlargement of size distributions induces an error in DLS sizing measurements: sizes are shifted to higher values compared with TEM analyses.36 The second reason is that the techniques based on light scattering like DLS require a higher concentration of NPs solution, which is more likely to lead to aggregation. Consequently, the aggregated NPs have a disproportionate influence on the analytical signal.37
The synthesis procedure of IONPs is greatly influenced by many factors, such as time, temperature, and solution pH, which must, therefore, be carefully controlled.38,39 These parameters and their effects on synthesized IONPs are listed in Table 2.40–44 In this study, we synthesized IONPs through a fast method, which took approximately 5 min to complete and did not require heating, which simplified the synthesis process.
Table 2 The effect of most crucial parameters in IONPs synthesis. The effect of an increase of these parameters (in an optimum range) was shown on bare IONPs characteristics
To obtain exhaustive information on in vivo G4@IONPs toxicity, blood chemistry and histological studies were performed. The results showed no significant histological abnormality in the hepatic and renal tissue; while, at concentration of 10 mg/kg, edema and losing cytoplasm were seen in the liver cells, which might be the result of an accumulation of G4@IONPs in the liver during 4 h after injection (1.92 ppm); furthermore, indirect bilirubin and BUN levels significantly increased at 10 mg/kg and 100 mg/kg, respectively. IONPs have been reported to be toxic at 60 mg/kg of body mass, while in our study the toxicity level of G4@IONPs was decreased (100 mg/kg), possibly due to dendrimer coating.45 IONPs are generally assumed to be biocompatible and non-toxic materials, as their LD50 (the dose needed to kill half of the tested animals during a specified time) was reported to be 200–600 mg Fe/kg body weight, while this value increased to 2,000–6,000 mg Fe/kg for dextran-coated IONPs.46
Our results showed good agreement with outcomes of other studies; as Jain et al12 assessed the toxicity of Pluronic coated IONPs with a hydrodynamic size of 186–206 nm in rats, by checking ALT, aspartate aminotransferase and ALP in serum after injection. Also, the amount of lipid hydroperoxide in different tissues was used to analyze the levels of their oxidative stresses due to the administration of the IONPs. They showed that the IONPs only caused minor transient changes, over a period of 6–24 h in the liver enzyme levels. Oxidative stress levels in different tissues also declined after 3 days. These results were also confirmed by histological analyses of the organs, which showed no apparent abnormal changes. In another study, Gu et al16 studied the in vivo toxicity of the monodisperse oleic acid capped IONPs with a size of 5, 15, and 30 nm, coated with a layer of phospholipid–PEG copolymer. One day after injection, the hematology results revealed an increase in the number of neutrophils which returned back to normal during the next 30 days. This was recognized as the host body defense response to the presence of IONPs. All the other parameters were without any change.
We also assessed the toxicity of G4@IONPs in cardiac muscle by TUNEL assay, because of the following reasons; an increase of LDH in the blood test, accumulation of a high amount of G4@IONPs in this tissue, and application of dendrimers in cardiovascular imaging.32,47 The results indicated that G4@IONPs could increase apoptosis at concentrations of 5 and 10 mg/kg.
Furthermore, no major change was noted in mice weight and mortality during the experiment time, similar to the other studies. For example, Malik et al48 found that three daily doses of G3.5 PAMAM (95 mg/kg) injected into C57 mice bearing B16F10 tumors had no adverse weight changing. In another study, no toxicity or mortality was seen when a single dose (up to 2.56 g/kg) of PEGylated melamine dendrimer was injected into male C3H mice. Also, BUN levels or transaminases remained unchanged.49
For biodistribution investigation, the concentration of G4@IONPs in different tissues was measured during 24 h. At this time point, the maximum amount of G4@IONPs accumulated in the lung and kidney tissues. It is worth mentioning that the most favorite excretion route for IONPs from the body is through the kidneys, which have negligible intracellular catabolism, so the probability of reactive oxygen species generation is low.2 Barry50 claimed that IONPs smaller than 50 nm evade opsonization and are then slowly collected by macrophages in RES; while in our study G4@IONPs were mainly taken up by the kidney tissue.
The results showed a decrease in accumulated G4@IONPs in all tissues 8 h after injection. The iron levels at this time declined to approximately half of the primary concentration, except the lung tissue, in which this decrease was only 14%. This might be due to a return of absorbed G4@IONPs to the bloodstream and then to the spleen or lymph nodes, while the inherent immune system in lungs acts as the main barrier against G4@IONPs and prevents them from returning to the bloodstream and other organs.51
The iron level detected in blood was highest 4 h after injection, while after 8 h this amount decreased. This might be because of accumulation of G4@IONPs inside the tissues. As mentioned before, at this time, also the amount of iron decreased in tissues so there was just a hypothesis that G4@IONPs was taken up by other tissues such as lymph nodes or the spleen. After 12 h, the amount of iron increased again and then, at the end of 24 h, this value reached approximately half of the primary amount (1.6 ppm).
There were some limitations in our study; first, the experiment duration to determine the biodistribution could have been longer than 24 h. In most tissues, a steady decline in G4@IONPs concentration was seen, so a longer duration might be necessary to study longer tissue distribution. Second, we did not measure the iron content in the spleen and lymph nodes, which are important organs in RES. Further research could elaborate on the biodistribution of the other generations of dendrimers.
IONPs are gradually being assessed for their potential in targeted drug delivery, magnetic hyperthermia, gene delivery, and as a contrast agent in MRI. A comprehensive clarification of their toxicity and clearance platform seems to be essential. This study indicated that dendrimers could be an appropriate coating for IONPs, due to their unique properties, such as acceptable toxicity, clearance pattern, and also long circulation time in the BALB/c mice. Obviously, there is a high demand to assess the toxicity and biokinetics of coated IONPs with the other dendrimer generations.
This research was supported by a grant from Tehran University of Medical Sciences (grant no. 28169).
The authors report no conflicts of interest in this work.
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