Open Access

Manufacture of IRDye800CW-coupled Fe3O4 nanoparticles and their applications in cell labeling and in vivo imaging

  • Yong Hou1, 2,
  • Yingxun Liu1,
  • Zhongping Chen1,
  • Ning Gu1 and
  • Jinke Wang1, 2Email author
Contributed equally
Journal of Nanobiotechnology20108:25

Received: 9 July 2010

Accepted: 29 October 2010

Published: 29 October 2010



In recent years, near-infrared fluorescence (NIRF)-labeled iron nanoparticles have been synthesized and applied in a number of applications, including the labeling of human cells for monitoring the engraftment process, imaging tumors, sensoring the in vivo molecular environment surrounding nanoparticles and tracing their in vivo biodistribution. These studies demonstrate that NIRF-labeled iron nanoparticles provide an efficient probe for cell labeling. Furthermore, the in vivo imaging studies show excellent performance of the NIR fluorophores. However, there is a limited selection of NIRF-labeled iron nanoparticles with an optimal wavelength for imaging around 800 nm, where tissue autofluorescence is minimal. Therefore, it is necessary to develop additional alternative NIRF-labeled iron nanoparticles for application in this area.


This study manufactured 12-nm DMSA-coated Fe3O4 nanoparticles labeled with a near-infrared fluorophore, IRDye800CW (excitation/emission, 774/789 nm), to investigate their applicability in cell labeling and in vivo imaging. The mouse macrophage RAW264.7 was labeled with IRDye800CW-labeled Fe3O4 nanoparticles at concentrations of 20, 30, 40, 50, 60, 80 and 100 μg/ml for 24 h. The results revealed that the cells were efficiently labeled by the nanoparticles, without any significant effect on cell viability. The nanoparticles were injected into the mouse via the tail vein, at dosages of 2 or 5 mg/kg body weight, and the mouse was discontinuously imaged for 24 h. The results demonstrated that the nanoparticles gradually accumulated in liver and kidney regions following injection, reaching maximum concentrations at 6 h post-injection, following which they were gradually removed from these regions. After tracing the nanoparticles throughout the body it was revealed that they mainly distributed in three organs, the liver, spleen and kidney. Real-time live-body imaging effectively reported the dynamic process of the biodistribution and clearance of the nanoparticles in vivo.


IRDye800CW-labeled Fe3O4 nanoparticles provide an effective probe for cell-labeling and in vivo imaging.


In the past decade, the synthesis of iron-based magnetic nanoparticles has rapidly developed for fundamental biomedical applications, including bioseparation [1, 2], MRI contrast enhancement [3, 4], hyperthermia [5, 6], and drug delivery [7, 8]. For example, the Fe3O4 nanoparticle has attracted great attentions for its potential theranostic applications [912]. As iron nanoparticles are administered to living subjects in most of their clinical applications, their in vivo biodistribution, clearance and biocompatibility must be determined for safe clinical usage. As such, in vivo studies of iron nanoparticles have made great progress in recent years.

In vivo studies of iron nanoparticles have mainly been performed using magnetic resonance imaging (MRI) [1318]. MRI is the most widely used technique for imaging magnetic nanoparticles in small animals and humans. A major advantage of MRI is that it can be used to perform real-time imaging of the dynamic biodistribution and clearance of magnetic nanoparticles in vivo. However, MRI is still prohibitive to the common research laboratory. Therefore, fluorescence imaging techniques have been developed and applied in studies of magnetic nanoparticles. Iron nanoparticles have been labeled with fluorophores, such as FITC [1921], rhodamine B [22, 23] and rhodamine 6G [18], resulting in the generation of bifunctional labeled nanoparticles, having both MRI and fluorescence imaging functions [24, 25]. Magnetic nanoparticles labeled with these conventional fluorophores (350-700 nm absorbing) have often been used to investigate the intracellular distribution of magnetic nanoparticles in cells [17, 18, 26]; however, these nanoparticles cannot be applied to in vivo imaging as the autofluorescence of tissues produce high background under excitation wavelengths less than 700 nm.

In recent years, near-infrared fluorescence (NIRF) imaging technology has been developed and progressively used to obtain biological functions of specific targets in vitro and in small animals [2729]. NIR fluorophores work in the spectrum of 700 to 900 nm, which has a low absorption by tissue chromophores [30]. Therefore, NIRF imaging has minimal background interference. NIR fluorophores also have wide dynamic range and sensitivity, allowing NIRF imaging to obtain detectable signal intensity through several centimeters of tissue [3133]. Based on these features, NIRF imaging has already been used to label nanoparticles and study their biodistribution, clearance and biocompatibility for in vivo biomedical applications. In a recent study, silica nanoparticles were labeled with DY776 and applied for in vivo bioimaging, biodistribution, clearance and toxicity analyses [34]. Furthermore, indocyanine green (ICG)-labeled calcium phosphate nanoparticles have been applied for imaging human breast cancer in vivo [35].

NIRF imaging has also been applied for the labeling of iron nanoparticles. Maxwell et al., used dextran-coated iron oxide nanoparticles (Feridex), covalently modified with Alexa Fluor 750, to label human hepatic stellate cells to monitor the engraftment process in vivo [36]. Furthermore, VivoTag 680-conjugated iron oxide particles have been intravenously injected into mice for imaging tumors [37]. Iron nanoparticles, labeled with Cy5.5 (excitation/emission (ex/em), 660/710 nm), have also been used as a MR contrast agent (CLIO) for sensoring the in vivo molecular environment surrounding the nanoparticles and tracing the in vivo biodistribution of CLIO in liver, spleen and kidneys [38]. Obviously, due to the excellent in vivo imaging performance of the NIR fluorophores, the NIRF-labeled iron nanoparticles provide a fine probe for the labeling of biomolecules or cells and in vivo imaging [3942]. However, there is still a limited selection of available iron nanoparticles labeled with NIRF dyes with an optimal wavelength for imaging in the region of 800 nm, where tissue autofluorescence is minimal. Therefore, it is necessary to develop additional alternative NIRF-labeled iron nanoparticles in this area.

This study manufactured water-soluble 12-nm Fe3O4 nanoparticles labeled with a new NIRF dye, IRDye800CW (Li-Cor Biosciences), which absorb and emit in higher wavelength light (ex/em, 774/789 nm), and investigated their applicability in cell labeling and in vivo imaging.

Results and discussions

Preparation of IRDy800CW-MNPs

M-2, 3-dimercaptosuccinic acid (DMSA) has often been used as a coating on nanoparticles to improve their water solubility [4346]. DMSA-coated nanoparticles have abundant carboxyls on their surface [4749], which can be used to label nanoparticles with fluorophores [23]. Using these features of DMSA, we fabricated novel nanoparticles by firstly creating water-soluble DMSA-coated Fe3O4 nanoparticles (MNPs), which were then reacted with ethyl-3, (3-di-methylaminopropyl carbodiimide) hydrochloride (EDC) to activate the surface carboxyl groups, following which we covalently crosslinked the NIRF dye, IRDy800CW, to the surface of the MNPs. The monodispersibility and size uniformity of MNPs and the IRDy800CW-labeled Fe3O4 nanoparticles (IRDy800CW-MNPs) in their prepared water solution were analyzed by TEM. The results demonstrated that both nanoparticles had fine monodispersibility (Figure 1A and 1B). The average size of the nanoparticles was 11.0 ± 1.25 nm in diameter.
Figure 1

Characterization of IRDy800CW-MNPs. (A) TEM image of MNPs. (B) TEM image of IRDy800CW-MNPs. (C) NIRF signal of nanoparticles. (D) Fluorescent spectrum of the nanoparticles. 1: IRDy800CW-MNPs; 2: MNPs. 3-4: The resuspended precipitate and supernatant of the IRDy800CW-MNPs solution after heat treatment and centrifugation. Abs: absorbance. Em: emission.

The labeling effect of MNPs was evaluated by detecting the NIRF signal of the IRDy800CW-MNPs. In comparison with unlabeled MNPs, the IRDy800CW-MNPs had an intense NIRF signal (Figure 1C). The excitation and emission profiles indicated a peak excitation/emission wavelength of the IRDye800CW-MNPs at 775/788 nm. The Stokes shift for the IRDye800CW-MNPs was 13 nm (Figure 1D). The covalent linkage between IRDy800CW and the MNPs was confirmed by a heating experiment (see Methods), in which the IRDy800CW-MNPs retained the NIRF signal after heat treatment (Figure 1C). If the IRDy800CW was nonspecifically absorbed on the surface of MNPs, the heating treatment would destroy this, resulting in the NIRF signal being found in the supernatant. This result accords with the molecular mechanism that EDC is a carboxyl and amine-reactive cross-linker, which creates an amide bond between carboxyl and amino groups [50].

In this study, the DMSA coating was important for the water solubility and NIRF labeling of the MNPs. Normally, the uncoated iron oxide nanoparticle has a very low solubility due to its hydrophobic surface [51, 52]. The DMSA coating makes the surface hydrophilic and dispersible in water solutions [4749, 5359]. Furthermore, this coating can also improve the biocompatability of iron oxide nanoparticles. In a recent study, DMSA-coated Fe2O3 nanoparticles were shown to have a low cytotoxicity [57], and have been used to label a variety of mammalian cells [4749, 55]. Conversely, DMSA-coated iron nanoparticles have abundant carboxyl groups on their surface, which is useful for the covalent labeling of nanoparticles by fluorescent dyes [23].

In this study, MNPs were labeled with a newly developed NIRF dye, IRDye800CW, which has several advantages. Firstly, IRDye800CW is a reactive dye [60], which can be easily conjugated to MNPs. This labeling approach can be generalized to other DMSA-coated nanoparticles. Secondly, the excitation and emission of IRDye800CW are in the spectral region where tissue absorption, autofluorescence, and scattering are minimal (800 nm), allowing for the highest signal-to-noise ratio to be achieved in tissue imaging with this dye. For example, IRDye800 absorbs and emits at a higher wavelength light (ex/em, 774/804 nm) than Cy5 (ex/em, 646/664 nm) and therefore produced images with less background resulting from tissue autofluorescence [61]. A comparison of the in vivo fluorescent imaging performance of the epidermal growth factor (EGF)-conjugated Cy5.5 (ex/em, 660/710 nm) and IRDye800CW (ex/em, 785/830 nm) revealed that the EGF-IRDye800CW had a significantly reduced background, with an enhanced the tumor-to-background ratio (TBR) in comparison to EGF-Cy5.5 [62]. Thirdly, this dye is highly water-soluble and shows very low nonspecific binding to cellular components, while yielding a very high signal [60, 63]. Fourthly, the animal toxicity studies revealed that a single intravenous administration of IRDye800CW carboxylate, at doses of 1, 5, and 20 mg/kg, produced no pathological evidence of toxicity [60]. Furthermore, the animal studies revealed that IRDye800CW and its conjugates were capable of fine in vivo imaging in small animal models, such as the mouse [6367]. IRDye800CW is also reported to be over 50 times brighter than ICG [68]. Based on these features, it is worth developing IRDye800CW-labeled iron nanoparticles as in vivo imaging probes with high signal-to-noise ratios.

Cell labeling with IRDy800CW-MNPs

Cell labeling with iron nanoparticles is very important for biomedical applications [36]. Therefore, this study firstly investigated the applicability of IRDy800CW-MNPs in this field. The macrophage is commonly used as a cellular model to evaluate intravascularly administered agents, especially as it phagocytoses nanoparticles [10]. Therefore, this study employed the mouse macrophage RAW264.7 cell line to perform a cell-labeling assay. The cells were labeled with nanoparticles at various concentrations for 24 h. The cell labeling effect was evaluated by staining cells with Prussian blue and measuring the iron-loading of cells. The Prussian blue staining showed that the cells were effectively labeled by the MNPs and the IRDy800CW-MNPs (Figure 2). The blue-stained agglomerates of the iron nanoparticles in cells increased with the dose of nanoparticles in the cell culture media (Figure 2), which was in accordance with the results of the quantitative measurements of the relative iron-loading of cells using colorimetric and NIRF assays (Figure 3). In comparison, the NIRF assay reported the cellular iron-loading more sensitively than the normal colorimetric assay [6972].
Figure 2

Prussian blue staining of cells. The agglomerates of Fe3O4 nanoparticles are stained in blue.

Figure 3

Measurement of the relative iron-loading of cells. (A) NIRF signal of cells labeled with IRDy800CW-MNPs at doses of 0, 20, 30, 40, 50, 60, 80 and 100 μg/ml (Column 1-8). Each dose contained 6 repeats (Row 1-6). Cells were washed with PBS before imaging. (B) Measurement of the relative iron-loading of cells (A) with colorimetric and NIRF approaches. Row 1-3: NIRF signals; Row 4-6: Colorimetric signals. (C) The intensity of colorimetric and NIRF signals (B). (D) The normalized intensity of colorimetric and NIRF signals (C). The signal of the nanoparticle-labeled cells was normalized to that of the negative control cell. The error bars represent mean and standard deviations of experiments performed in triplicate.

The biocompatability of cells to the nanoparticles is also important to its applications. Therefore, we used an MTT assay to determine cell viability following treatment with the nanoparticles. The results revealed that the cell viability of RAW264.7 was not significantly (p > 0.05) affected by the various doses of both MNPs and IRDy800CW-MNPs (Figure 4). In comparison with MNPs, the IRDy800CW-labeling did not bring toxicity to the MNPs. These results demonstrate that the IRDy800CW-MNPs have increased biocompatability. A dose of 30 μg/ml of the nanoparticles used in this MTT assay corresponds to the optimal blood concentration of a nanoparticle imaging agent, Combidexe, which has been intravascularly administered in humans at 2.6 mg Fe/kg body weight [10, 73].
Figure 4

Measurement of cell viability. (A) NIRF signals of cells treated with MNPs (Column 1-3 and 10-12) and IRDy800CW-MNPs (Column 4-9) at doses of 0, 20, 30, 40, 50, 60, 80 and 100 μg/ml (From row 1-8) for 24 h. (B) NIRF signals of cells (A) after washing three times with PBS. (C) Quantitative measurement of cell viability by MTT assay. The error bars represent mean and standard deviations of experiments performed with 6 repeats.

In vivo imaging with IRDy800CW-MNPs

Animal studies are indispensable to the clinical applications of nanoparticles. The biodistribution, metabolism, clearance and toxicity of nanoparticles must be examined in animal studies prior to their clinical application. In particular, these biological processes should be investigated in a dynamic and real-time form with living animals. In recent years, NIRF labeling has played an increasingly important role in in vivo studies [2833]. Therefore, this study investigated the applicability of the IRDy800CW-MNPs in this field.

The in vivo studies were performed in a mouse model and employed a newly developed optical imaging instrument dedicated to small animal imaging, the Pearl Imager (LI-COR Biosciences) [74]. To obtain fine imaging effects, a naked mouse was used in this study. The mouse was first imaged prior to the administration of the nanoparticles to determine the value of the self-fluorescence background. Following this, the mouse was intravascularly administered IRDy800CW-MNPs at doses of 2 or 5 mg/kg body weight. The mouse was then discontinuously imaged at different time points. The real-time imaging of the mouse showed that the NIRF signal in the liver region and kidneys gradually intensified after injection of nanoparticles, reaching maximum levels at 6 h (Figure 5, 6 and 7), thereby demonstrating a gradual enrichment of the IRDy800CW-MNPs in these regions. Following this, the NIRF signal in these regions gradually decreased, revealing a gradual clearance of the IRDy800CW-MNPs. These results demonstrate that the whole dynamic process of biodistribution and clearance of MNPs in the mouse model could be monitored and tracked by the IRDy800CW labels and the small animal NIRF-imaging system, Pearl Image.
Figure 5

NIRF imaging of a mouse administered IRDye800CW-MNPs at a dose of 2 mg/kg body weight. The images are displayed in pseudo-color mode.

Figure 6

NIRF imaging of a mouse administered the IRDy800CW-MNPs at a dose of 5 mg/kg body weight. The images are displayed in pseudo-color mode.

Figure 7

NIRF imaging of a mouse administered the IRDye800CW-MNPs at a dose of 5 mg/kg body weight. The images are displayed in an overlay mode of light channel image and NIRF channel image.

NIRF imaging of the mouse also clearly revealed that the intensity of signal in the liver region and kidneys was closely related to the dose of the intravenously injected IRDy800CW-MNPs. In comparison, the intensity of the NIRF signals in the liver and kidneys of the mouse injected with 2 mg/kg nanoparticles was much higher than that of the mouse injected with 5 mg/kg nanoparticles (Figure 5 and 6). This signal/dose relationship may be used to investigate the metabolism efficiency of the different doses of nanoparticles.

To clarify the exact biodistribution of nanoparticles in different organs, the mouse was sacrificed after imaging for 5 days, and the organs, including the heart, lungs, liver, spleen and kidneys were isolated and their NIRF signal was measured. The results revealed that the IRDy800CW-MNPs mainly distributed in the liver, spleen and kidneys (Figure 8), with minimal distribution in the heart and lungs. This agrees with the results of whole body imaging. It can be found that the intense NIRF signal in the liver region, as measured by live-body imaging, actually comes from two organs, the liver and spleen. The liver is the largest organ in the body of a mouse and the spleen is far smaller, but the spleen is closely attached to the liver; therefore, it cannot be discerned from the liver in the live-body imaging. However, the organ imaging clearly revealed its importance in evaluating the biodistribution of the nanoparticles. Taken together, the individual NIRF imaging of organs is an important supplement to live-body imaging, as it revealed that the in vivo biodistribution and clearance of the MNPs mainly related to these three organs.
Figure 8

NIRF imaging of organs of a IRDy800CW-MNPs-injected mouse. (A) Light images of heart, lung, liver, spleen and kidney of the mouse administered the IRDye800CW-MNPs. (B) NIRF images of the same organs.

In previous studies, it was found that the magnetic nanoparticles were mainly distributed in the liver and spleen [13, 17, 18, 26, 7577]. This pattern of biodistribution is independent of the routes of administration, such as intravenous injection [1315, 18, 53, 75, 78, 79], intraperitoneal injection [26], intratracheally instillation [77], and inhalation [17]. These results are in agreement with our findings herein. The common highest distribution of various iron magnetic nanoparticles in liver and spleen closely relates to the reticulo-endothelial system (RES), also known as the mononuclear phagocytic system (MPS). The RES contains abundant phagocytic cells which can remove particulate materials from blood [80]. Therefore, the RES plays an important role in the biodistribution and clearance of nanoparticles in vivo [26, 76, 81, 82]. Furthermore, the liver and spleen are the major RES organs in body, with Kupffer cells and macrophages being their main RES members, respectively. It was reported that over 75% of the magnetic nanoparticles were promptly sequestered by the RES, particularly by the liver [83]. It was also reported that after 6 h following administration, approximately 55% iron nanoparticles were enriched in the liver by the RES [76]. TEM observation of the liver and spleen revealed that Kupffer cells contained an increasing number of progressively larger phagolysosomes containing magnetic nanoparticles 7 days after injection, and the macrophages in the spleen contained magnetic nanoparticles in lysosomes [79]. It was also reported that the USPIO accumulated in macrophages of the liver, spleen, lymph nodes and bone marrow [14, 73, 84, 85].

It was also reported that the magnetic nanoparticles were able to distribute in the kidneys, lungs, heart, brain, testes, uterus, ovary, bladder, thyroid, pancreas, and bone marrow [14]. However, the amount of nanoparticles distributed in these organs or tissues was far less than that in liver and spleen. This study revealed that the IRDy800CW-MNPs were also enriched in the kidneys. This may be related to the biological function of the kidneys, which is an important emunctory containing large a volume of blood undergoing filtration. The large difference in the NIRF intensity between the kidneys of mice injected with different doses of the IRDy800CW-MNPs (Figure 8) also demonstrated that the kidneys may play an important role in the biodistribution and clearance of iron nanoparticles.

The dose of the IRDy800CW-MNPs used in the in vivo imaging in this study is similar to those reported by other studies. The magnetic nanoparticles were reported to be intravascularly administered to mouse or rat at doses of 1 [15], 2 [15, 83], 3 [86], 5 [15, 87], and 10 mg Fe/kg body weight [76]. It was also reported that an intravascular nanoparticle imaging agent, Combidexe, was injected at 2.6 mg of Fe/kg body weight to humans for MRI [73].

This study did not measure physiological indexes and therefore cannot comment on any possible or potential effects of the IRDy800CW-MNPs to the health of mouse. However, careful observation of the mouse's behavior over the five days of in vivo imaging revealed that injection of the nanoparticles did not result in any observed adverse effects on activity, eating or drinking of the mouse. This implies that the IRDy800CW-MNPs may have better biocompatability to mice, which is the key small animal employed for the biomedical research of iron nanoparticles.


This study manufactured water-soluble 12-nm DMSA-coated Fe3O4 nanoparticle labeled with a NIRF dye, IRDye800CW, and investigated its applicability in cell labeling and living body imaging. The results demonstrate that the IRDye800CW-labeled Fe3O4 nanoparticles effectively labeled a RAW264.7 cell, but did not significantly affect the cell viability. The animal studies demonstrate that the IRDye800CW-labeled Fe3O4 nanoparticles could sensitively and in real-time monitor the whole dynamic process of the biodistribution and clearance of the Fe3O4 nanoparticles in mouse. Therefore, IRDye800CW-labeled Fe3O4 nanoparticles provide a new selection of available iron nanoparticles labeled with NIRF dyes with an optimal wavelength for imaging centered at 800 nm, which can be applied to in vitro cell labeling and in vivo imaging.


Cells, animals and chemicals

The RAW264.7 cell line was purchased from the China Center for Type Culture Collection, Chinese Academy of Sciences (Shanghai, China). DMEM cell culture medium was purchased from Gibco, Invitrogen (CA, USA). The naked mouse (CByJ-Cg-Foxn1nu/J) was purchased from Model Animal Research Center of Nanjing, Nanjing University (Nanjing, China). The streptavidin-IRDye 800CW was purchased from Li-Cor Biosciences (Lincoln, NE, USA). The main chemicals, including EDC, HEPES, glutaraldehyde and paraformaldehyde, were purchased from Sigma Aldrich (MO, USA). Other chemicals, including potassium peroxydisulfate (K2S2O8), potassium ferrocyanide (KSCN), iron (III) chloride hexahydrate (FeCl3), and hydrochloric acid, were purchased from Sinopharm Chemical Reagent Co. Ltd (Shanghai, China).

Preparation of IRDy800CW-MNPs

The water-soluble Fe3O4 nanoparticles were synthesized under the following conditions. Firstly, 2.7 g of FeCl3•6H2O was dissolved in 50 ml of methanol, followed by the addition of 8.5 ml oleic acid. Then, a solution with 1.2 g of NaOH in 100 ml methanol was dropwise added into the solution under magnetic stirring conditions. The observed brown precipitate was washed with methanol 4-5 times and dried under vacuum overnight to remove all solvents. The obtained waxy iron-oleate was dissolved in 1-octadecanol at 70°C and reserved as a stable stock solution at room temperature. One milliliter of the stock solution (0.39 mM) was mixed with 4 ml 1-octadecanol and 0.5 ml oleic acid. The reaction mixture was heated to 320°C at a constant heating rate of 3.3°C/min, in a nitrogen atmosphere, and maintained at that temperature for 30 min. The resulting solution was cooled and precipitated by an addition of excess ethanol and centrifugation. The precipitate containing Fe3O4 nanoparticles was washed 4-5 times with ethanol. To prepare water-soluble Fe3O4 nanoparticles, 100 mg of above Fe3O4 nanoparticles was dissolved in 10 ml chloroform, following which 50 μl triethylamine and 10 ml dimethyl sulfoxide (DMSO) containing 50 mg dispersed DMSA was added. The resulting solution was vortexed at 60°C for 12 h until a black precipitate was observed. The solution was subsequently centrifuged and the precipitate was carefully washed twice with ethanol and dissolved in 100 ml ethanol. To introduce more DMSA molecules onto the surface of Fe3O4 nanoparticles, 50 μl triethylamine was added to the above ethanol solution containing Fe3O4 nanoparticles, followed by the addition of a solution with 50 mg DMSA in 10 ml DMSO. The solution was again vortexed at 60°C for 12 h. The reaction solution was then centrifuged and the precipitate washed with ethanol 4-5 times carefully. The final MNPs were collected using a permanent magnet and transferred into 10 ml water.

The MNPs were labeled with NIR fluorophores by the following procedure. Six ml of nanoparticles (0.844 mg/ml Fe) were diluted into 24 ml and sonicated for 20 min. Following this, 10 mg EDC was added and sonicated for 40 min to activate the carboxyl groups on the surface of the nanoparticles. The solution was centrifuged at 12000 rpm for 10 min and the precipitate was resuspended in sterile deionized water. Then, 15 μl of Streptavidin-IRDye800CW was added to the resuspended nanoparticles and the nanoparticle solution was left on a rotator overnight. The nanoparticle solution was centrifuged at 12000 rpm for 10 min and the precipitate was washed 3 times with deionized water. Finally, the IRDye800CW-MNPs were resuspended in sterile deionized water.

The monodispersibility of MNPs and the IRDye800CW-MNPs was evaluated by TEM. Each of nanoparticles in the 30 μg/ml sample was added to a copper grid and observed with a JEM-2100 electron microscope (JEOL, Japan). The size of the nanoparticles was measured with Image Origin 6.1. The NIRF signal of the nanoparticles was detected with Odyssey Infrared Imaging System (Li-Cor). The fluorescent spectrum of the nanoparticles was measured using a Hitachi F-7000 Fluorescence Spectrophotometer. To verify that the IRDy800CW was covalently crosslinked to the nanoparticles and not by nonspecific absorption, the solution of NIRF-labeled nanoparticles was heated at 60°C for 15 min, and centrifuged to precipitate the nanoparticles. The supernatant and nanoparticles were collected separately, and the nanoparticles were resuspended in deionized water. The supernatants and the resuspended nanoparticles were detected with Odyssey Infrared Imaging System.

Cell labeling with IRDy800CW-MNPs

To investigate the labeling of cells with nanoparticles, RAW264.7 cells were seeded into cell culture plates and cultured in DMEM supplemented with 10% fetal calf serum, penicillin (100 units/ml), streptomycin (100 μg/ml) and 10 mM HEPES in a humidified 5% CO2 atmosphere at 37°C for 24 h. Then, the culture medium was discarded and the cells were cultured with fresh media containing nanoparticles at different doses for 24 h.

The labeling effects were evaluated by staining cells with Prussian blue and measurement of the iron-loading of cells. Prussian blue staining, which stains iron nanoparticles blue, was performed as previously described [4749, 5457]. The stained cells were observed with a light microscope (IX51, Olympus) and photographed using a Microscope Digital Camera (DP71, Olympus). The iron-loading of cells was measured with a common colorimetric assay, as previously described [6972]. The iron-loading of the cells labeled by the IRDy800CW-MNPs was also evaluated by the NIRF signal. To measure the NIRF signal, cells were washed with PBS and lysed using SDS lysis buffer. The lysate was imaged and NIRF signal intensity was analyzed using the Odyssey Infrared Imaging System (Li-Cor).

The effect of labeling on the cell proliferation was evaluated by determining cell viability, which was assessed using a MTT assay, as reported elsewhere [8284]. The cell viability of the nanoparticle-untreated cells (blank control) was defined as 100%, with the nanoparticle-treated cells being calculated as percentage of the control.

In vivo imaging with IRDy800CW-MNPs

Before injection of the IRDy800CW-MNPs, the mouse was imaged on a newly-developed infrared fluorescence imaging system, Pearl Image (Li-Cor). Subsequently, the mouse was anesthetized by ether inhalation and the IRDy800CW-MNPs were administered to the mouse by intravascular injection via the tail vein, at doses of 2 or 5 mg Fe/kg body weight. The mouse was housed under normal conditions and discontinuously imaged with Pearl Image at various time points. Just before each image acquisition, the mouse was anesthetized by ether inhalation. All images were captured at the same exciting intensity. After housing and imaging for 5 days following the injection of nanoparticles, the mouse was sacrificed by an overdose of anesthesia and the organs, including the heart, lungs, liver, spleen and kidneys were immediately collected. The organs were washed with PBS and imaged with a normal camera and Odyssey Infrared Imaging System (Li-Cor).




Magnetic resonance imaging


near infrared fluorescence


indocyanine green


Phosphate Buffer Solution


Sodium dodecyl sulfate


transmission electron microscopy


Dulbecco's modified Eagle medium


a form of MION (monocrystalline iron oxide nanoparticles) with cross-linked dextran coating: USPIO: dextran-coated SPIO (superparamagnetic iron oxide)


1-ethyl-3,(3-di-methylaminopropyl carbodiimide) hydrochloride


m-2,3-dimercaptosuccinic acid


3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide



This study was partially funded by the National Important Science Research Program of China (2006CB933205) and the China International Science and Technology Cooperation (2009DFA31990). We thank Gene Company Limited (Shanghai) for use of the Pearl Image equipment and guidance in the in vivo study.

Authors’ Affiliations

State key Laboratory of Bioelectronics, Southeast University
Experimental Center of Biotechnology and Biomaterials, BME, Southeast University


  1. Lewin M, Carlesso N, Tung CH, Tang XW, Cory D, Scadden DT, Weissleder R: Tat peptide-derivatized magnetic nanoparticles allow in vivo tracking and recovery of progenitor cells. Nat Biotechnol. 2000, 18: 410-414. 10.1038/74464.View ArticleGoogle Scholar
  2. Nam JM, Thaxton CS, Mirkin CA: Nanoparticle-based bio-bar codes for the ultrasensitive detection of proteins. Science. 2003, 301: 1884-1886. 10.1126/science.1088755.View ArticleGoogle Scholar
  3. Weissleder R, Moore A, Mahmood U, Bhorade R, Benveniste H, Chiocca EA, Basilion JP: In vivo magnetic resonance imaging of transgene expression. Nat Med. 2000, 6: 351-355. 10.1038/73219.View ArticleGoogle Scholar
  4. Tiefenauer L: Magnetic Nanoparticles as Contrast Agents for Medical Diagnosis. Nanotechnology in Biology and Medicine. Edited by: Tuan Vo-Dinh. 2007, Boca Raton: CRC Press, 29/10Google Scholar
  5. Ito A, Shinkai M, Honda H, Kobayashi T: Heat-inducible TNF-alpha gene therapy combined with hyperthermia using magnetic nanoparticles as a novel tumor-targeted therapy. Cancer Gene Ther. 2001, 8: 649-654. 10.1038/sj.cgt.7700357.View ArticleGoogle Scholar
  6. Hergt R, Dutz S: Magnetic particle hyperthermia-biophysical limitations of a visionary tumour therapy. J Magn Magn Mater. 2007, 311: 187-192. 10.1016/j.jmmm.2006.10.1156.View ArticleGoogle Scholar
  7. Lin BL, Shen XD, Cui S: Application of nanosized Fe3O4 in anticancer drug carriers with target-orientation and sustained-release properties. Biomed Mater. 2007, 2: 132-134. 10.1088/1748-6041/2/2/011.View ArticleGoogle Scholar
  8. Shubayev VI, Pisanic TR, Jin S: Magnetic nanoparticles for theragnostics. Adv Drug Deliv Rev. 2009, 61: 467-477. 10.1016/j.addr.2009.03.007.View ArticleGoogle Scholar
  9. Pankhurst QA, Connolly J, Jones SK, Dobson J: Applications of magnetic nanoparticles in biomedicine. J Phys D Appl Phys. 2003, 36: R167-R181. 10.1088/0022-3727/36/13/201.View ArticleGoogle Scholar
  10. Shaw SY, Westly EC, Pittet MJ, Subramanian A, Schreiber SL, Weissleder R: Perturbational profiling of nanomaterial biologic activity. Proc Natl Acad Sci. 2008, 105: 7387-7392. 10.1073/pnas.0802878105.View ArticleGoogle Scholar
  11. Bacon BR, Stark DD, Park CH, Saini S, Groman EV, Hahn PF, Compton CC, Ferrucci JT: Ferrite particles: a new magnetic resonance imaging contrast agent. Lack of acute or chronic hepatotoxicity after intravenous administration. J Lab Clin Med. 1987, 110: 164-171.Google Scholar
  12. Weissleder R, Stark DD, Engelstad BL, Bacon BR, Compton CC, White DL, Jacobs P, Lewis J: Superparamagnetic iron oxide: pharmacokinetics and toxicity. AJR Am J Roentgenol. 1989, 152: 167-173.View ArticleGoogle Scholar
  13. Lacava LM, Lacava ZGM, Azevedo RB, Chaves SB, Garcia VAP, Silva O, Pelegrini F, Buske N, Gansau C, Da Silva MF, Morais PC: Use of magnetic resonance to study biodistribution of dextran-coated magnetic fluid intravenously administered in mice. J Magn Magn Mater. 2002, 252: 367-369. 10.1016/S0304-8853(02)00654-6.View ArticleGoogle Scholar
  14. Lacava LM, Garcia VAP, Kuckelhaus S, Azevedo RB, Lacava ZGM, Silva O, Pelegrini F, Gansau C, Buske N, Morais PC: Magnetic resonance and light microscopy investigation of a dextran coated magnetic fluid. J Appl Phys. 2003, 93: 7563-7565. 10.1063/1.1540178.View ArticleGoogle Scholar
  15. Briley-Saebo K, Bjornerud A, Grant D, Ahlstrom H, Berg T, Kindberg GM: Hepatic cellular distribution and degradation of iron oxide nanoparticles following single intravenous injection in rats: implications for magnetic resonance imaging. Cell and Tissue Res. 2004, 316: 315-323. 10.1007/s00441-004-0884-8.View ArticleGoogle Scholar
  16. Kalber TL, Smith CJ, Howe FA, Griffiths JR, Ryan AJ, Waterton JC, Robinson SP: A longitudinal study of R2* and R2 magnetic resonance imaging relaxation rate measurements in murine liver after a single administration of 3 different iron oxide-based contrast agents. Invest Radiol. 2005, 40: 784-791. 10.1097/01.rli.0000188025.66872.e4.View ArticleGoogle Scholar
  17. Kwon JT, Hwang SK, Jin H, Kim DS, Minai-Tehrani A, Yoon HJ, Choi M, Yoon TJ, Han DY, Kang YW: Body distribution of inhaled fluorescent magnetic nanoparticles in the mice. J Occup Health. 2008, 50: 1-6. 10.1539/joh.50.1.View ArticleGoogle Scholar
  18. Lee PW, Hsu SH, Wang JJ, Tsai JS, Lin KJ, Wey SP, Chen FR, Lai CH, Yen TC, Sung HW: The characteristics, biodistribution, magnetic resonance imaging and biodegradability of superparamagnetic core-shell nanoparticles. Biomaterials. 2010, 31: 1316-1324. 10.1016/j.biomaterials.2009.11.010.View ArticleGoogle Scholar
  19. Hatanaka S, Matsushita N, Abe M, Nishimura K, Hasegawa M, Handa H: Direct immobilization of fluorescent dyes onto ferrite nanoparticles during their synthesis from aqueous solution. J Appl Phys. 2003, 93: 7569-7570. 10.1063/1.1558677.View ArticleGoogle Scholar
  20. Yoon TJ, Kim JS, Kim BG, Yu KN, Cho MH, Lee JK: Multifunctional nanoparticles possessing a "magnetic motor effect" for drug or gene delivery. Angew Chem Int Ed Engl. 2005, 44: 1068-1071. 10.1002/anie.200461910.View ArticleGoogle Scholar
  21. Guo J, Yang W, Deng Y, Wang C, Fu S: Organic-dye-coupled magnetic nanoparticles encaged inside thermoresponsive PNIPAM Microcapsules. Small. 2005, 1: 737-743. 10.1002/smll.200400145.View ArticleGoogle Scholar
  22. Kwon JT, Kim DS, Minai-Tehrani A, Hwang SK, Chang SH, Lee ES, Xu CX, Lim HT, Kim JE, Yoon BI: Inhaled fluorescent magnetic nanoparticles induced extramedullary hematopoiesis in the spleen of mice. J Occup Health. 2009, 51: 423-431. 10.1539/joh.L8159.View ArticleGoogle Scholar
  23. Bertorelle F, Wilhelm C, Roger J, Gazeau F, Menager C, Cabuil V: Fluorescence-modified superparamagnetic nanoparticles: intracellular uptake and use in cellular imaging. Langmuir. 2006, 22: 5385-5391. 10.1021/la052710u.View ArticleGoogle Scholar
  24. Laemmel E, Genet M, Le Goualher G, Perchant A, Le Gargasson JF, Vicaut E: Fibered confocal fluorescence microscopy (Cell-viZio) facilitates extended imaging in the field of microcirculation. A comparison with intravital microscopy. J Vasc Res. 2004, 41: 400-411. 10.1159/000081209.View ArticleGoogle Scholar
  25. Lim YT, Kim S, Nakayama A, Stott NE, Bawendi MG, Frangioni JV: Selection of quantum dot wavelengths for biomedical assays and imaging. Mol Imaging. 2003, 2: 50-64. 10.1162/153535003765276282.View ArticleGoogle Scholar
  26. Kim JS, Yoon TJ, Yu KN, Kim BG, Park SJ, Kim HW, Lee KH, Park SB, Lee JK, Cho MH: Toxicity and tissue distribution of magnetic nanoparticles in mice. Toxicol Sci. 2006, 89: 338-347. 10.1093/toxsci/kfj027.View ArticleGoogle Scholar
  27. Frangioni JV: In vivo near-infrared fluorescence imaging. Curr Opin Chem Biol. 2003, 7: 626-634. 10.1016/j.cbpa.2003.08.007.View ArticleGoogle Scholar
  28. Achilefu S: Lighting up tumors with receptor-specific optical molecular probes. Technol Cancer Res Treat. 2004, 3: 393-409.View ArticleGoogle Scholar
  29. Ntziachristos V, Bremer C, Weissleder R: Fluorescence imaging with near-infrared light: new technological advances that enable in vivo molecular imaging. Eur Radiol. 2003, 13: 195-208.Google Scholar
  30. Weissleder R: A clearer vision for in vivo imaging. Nat Biotechnol. 2001, 19: 316-317. 10.1038/86684.View ArticleGoogle Scholar
  31. Loo C, Lowery A, Halas N, West J, Drezek R: Immunotargeted nanoshells for integrated cancer imaging and therapy. Nano Lett. 2005, 5: 709-711. 10.1021/nl050127s.View ArticleGoogle Scholar
  32. Sevick-Muraca EM, Houston JP, Gurfinkel M: Fluorescence-enhanced, near infrared diagnostic imaging with contrast agents. Curr Opin Chem Biol. 2002, 6: 642-650. 10.1016/S1367-5931(02)00356-3.View ArticleGoogle Scholar
  33. Weissleder R, Ntziachristos V: Shedding light onto live molecular targets. Nat Med. 2003, 9: 123-128. 10.1038/nm0103-123.View ArticleGoogle Scholar
  34. Kumar R, Roy I, Ohulchanskky TY, Vathy LA, Bergey EJ, Sajjad M, Prasad PN: In Vivo Biodistribution and Clearance Studies Using Multimodal Organically Modified Silica Nanoparticles. ACS Nano. 2010, 4: 699-708. 10.1021/nn901146y.View ArticleGoogle Scholar
  35. Altinoglu EI, Russin TJ, Kaiser JM, Barth BM, Eklund PC, Kester M, Adair JH: Near-infrared emitting fluorophore-doped calcium phosphate nanoparticles for in vivo imaging of human breast cancer. ACS Nano. 2008, 2: 2075-2084. 10.1021/nn800448r.View ArticleGoogle Scholar
  36. Maxwell DJ, Bonde J, Hess DA, Hohm SA, Lahey R, Zhou P, Creer MH, Piwnica-Worms D, Nolta JA: Fluorophore-conjugated iron oxide nanoparticle labeling and analysis of engrafting human hematopoietic stem cells. Stem Cells. 2008, 26: 517-524. 10.1634/stemcells.2007-0016.View ArticleGoogle Scholar
  37. McCann CM, Waterman P, Figueiredo JL, Aikawa E, Weissleder R, Chen JW: Combined magnetic resonance and fluorescence imaging of the living mouse brain reveals glioma response to chemotherapy. Neuroimage. 2009, 45: 360-369. 10.1016/j.neuroimage.2008.12.022.View ArticleGoogle Scholar
  38. Josephson L, Kircher MF, Mahmood U, Tang Y, Weissleder R: Near-infrared fluorescent nanoparticles as combined MR/optical imaging probes. Bioconjug Chem. 2002, 13: 554-560. 10.1021/bc015555d.View ArticleGoogle Scholar
  39. Jaffer FA, Nahrendorf M, Sosnovik D, Kelly KA, Aikawa E, Weissleder R: Cellular imaging of inflammation in atherosclerosis using magnetofluorescent nanomaterials. Mol Imaging. 2006, 5: 85-92.Google Scholar
  40. Montet X, Ntziachristos V, Grimm J, Weissleder R: Tomographic fluorescence mapping of tumor targets. Cancer Res. 2005, 65: 6330-6336. 10.1158/0008-5472.CAN-05-0382.View ArticleGoogle Scholar
  41. Jaffer FA, Sosnovik DE, Nahrendorf M, Weissleder R: Molecular imaging of myocardial infarction. J Mol Cell Cardiol. 2006, 41: 921-933. 10.1016/j.yjmcc.2006.09.008.View ArticleGoogle Scholar
  42. Funovics M, Montet X, Reynolds F, Weissleder R, Josephson L: Nanoparticles for the optical imaging of tumor E-selectin. Neoplasia. 2005, 7: 904-911. 10.1593/neo.05352.View ArticleGoogle Scholar
  43. Chen ZP, Zhang Y, Zhang S, Xia JG, Liu JW, Xu K, Gu N: Preparation and characterization of water-soluble monodisperse magnetic iron oxide nanoparticles via surface double-exchange with DMSA. Colloid Surf A. 2008, 316: 210-216. 10.1016/j.colsurfa.2007.09.017.View ArticleGoogle Scholar
  44. Kalambur VS, Longmire EK, Bischof JC: Cellular level loading and heating of superparamagnetic iron oxide nanoparticles. Langmuir. 2007, 23: 12329-12336. 10.1021/la701100r.View ArticleGoogle Scholar
  45. Rad AM, Janic B, Iskander A, Soltanian-Zadeh H, Arbab AS: Measurement of quantity of iron in magnetically labeled cells: comparison among different UV/VIS spectrometric methods. Biotechniques. 2007, 43: 627-628. 10.2144/000112599. 630, 632 passimView ArticleGoogle Scholar
  46. Hafelli UO, Riffle JS, Harris-Shekhawat L, Carmichael-Baranauskas A, Mark F, Dailey JP, Bardenstein D: Cell Uptake and in Vitro Toxicity of Magnetic Nanoparticles Suitable for Drug Delivery. Mol Pharm. 2009, 6: 1417-1428. 10.1021/mp900083m.View ArticleGoogle Scholar
  47. Auffan M, Decome L, Rose J, Orsiere T, De Meo M, Briois V, Chaneac C, Olivi L, Berge-Lefranc JL, Botta A: In vitro interactions between DMSA-coated maghemite nanoparticles and human fibroblasts: A physicochemical and cyto-genotoxical study. Environ Sci Technol. 2006, 40: 4367-4373. 10.1021/es060691k.View ArticleGoogle Scholar
  48. Ju SH, Teng GJ, Zhang Y, Ma M, Chen F, Ni YC: In vitro labeling and MRI of mesenchymal stem cells from human umbilical cord blood. Magn Reson Imaging. 2006, 24: 611-617. 10.1016/j.mri.2005.12.017.View ArticleGoogle Scholar
  49. Song M, Moon WK, Kim Y, Lim D, Song IC, Yoon BW: Labeling efficacy of superparamagnetic iron oxide nanoparticles to human neural stem cells: Comparison of ferumoxides, monocrystalline iron oxide, cross-linked iron oxide (CLIO)-NH2 and tat-CLIO. Korean J Radiol. 2007, 8: 365-371. 10.3348/kjr.2007.8.5.365.View ArticleGoogle Scholar
  50. Nakajima N, Ikada Y: Mechanism of Amide Formation by Carbodiimide for Bioconjugation in Aqueous-Media. Bioconjugate Chem. 1995, 6: 123-130. 10.1021/bc00031a015.View ArticleGoogle Scholar
  51. Fauconnier N, Pons JN, Roger J, Bee A: Thiolation of maghemite nanoparticles by dimercaptosuccinic acid. J Colloid Interface Sci. 1997, 194: 427-433. 10.1006/jcis.1997.5125.View ArticleGoogle Scholar
  52. Valois CRA, Braz JM, Nunes ES, Vinolo MAR, Lima ECD, Curi R, Kuebler WM, Azevedo RB: The effect of DMSA-functionalized magnetic nanoparticles on transendothelial migration of monocytes in the murine lung via a beta(2) integrin-dependent pathway. Biomaterials. 2010, 31: 366-374. 10.1016/j.biomaterials.2009.09.053.View ArticleGoogle Scholar
  53. Chaves SB, Lacava LM, Lacava ZGM, Silva O, Pelegrini F, Buske N, Gansau C, Morais PC, Azevedo RB: Light microscopy and magnetic resonance characterization of a DMSA-coated magnetic fluid in mice. IEEE T MAGN. 2002, 38: 3231-3233. 10.1109/TMAG.2002.802495.View ArticleGoogle Scholar
  54. Frank JA, Miller BR, Arbab AS, Zywicke HA, Jordan EK, Lewis BK, Bryant LH, Bulte JWM: Clinically applicable labeling of mammalian and stem cells by combining; Superparamagnetic iron oxides and transfection agents. Radiology. 2003, 228: 480-487. 10.1148/radiol.2281020638.View ArticleGoogle Scholar
  55. Riviere C, Boudghene FP, Gazeau F, Roger J, Pons JN, Laissy JP, Allaire E, Michel JB, Letourneur D, Deux JF: Iron oxide nanoparticle-labeled rat smooth muscle cells: Cardiac MR imaging for cell graft monitoring and quantitation. Radiology. 2005, 235: 959-967. 10.1148/radiol.2353032057.View ArticleGoogle Scholar
  56. Wilhelm C, Billotey C, Roger J, Pons JN, Bacri JC, Gazeau F: Intracellular uptake of anionic superparamagnetic nanoparticles as a function of their surface coating. Biomaterials. 2003, 24: 1001-1011. 10.1016/S0142-9612(02)00440-4.View ArticleGoogle Scholar
  57. Wilhelm C, Gazeau F: Universal cell labelling with anionic magnetic nanoparticles. Biomaterials. 2008, 29: 3161-3174. 10.1016/j.biomaterials.2008.04.016.View ArticleGoogle Scholar
  58. Wilhelm C, Gazeau F, Bacri JC: Magnetophoresis and ferromagnetic resonance of magnetically labeled cells. Eur Biophys J. 2002, 31: 118-125. 10.1007/s00249-001-0200-4.View ArticleGoogle Scholar
  59. Wilhelm C, Gazeau F, Roger J, Pons JN, Bacri JC: Interaction of anionic superparamagnetic nanoparticles with cells: Kinetic analyses of membrane adsorption and subsequent internalization. Langmuir. 2002, 18: 8148-8155. 10.1021/la0257337.View ArticleGoogle Scholar
  60. Marshall MV, Draney D, Sevick-Muraca EM, Olive DM: Single-Dose Intravenous Toxicity Study of IRDye 800CW in Sprague-Dawley Rats. Mol Imaging Biol. 2010Google Scholar
  61. Blum G, von Degenfeld G, Merchant MJ, Blau HM, Bogyo M: Noninvasive optical imaging of cysteine protease activity using fluorescently quenched activity-based probes. Nat Chem Biol. 2007, 3: 668-677. 10.1038/nchembio.2007.26.View ArticleGoogle Scholar
  62. Adams KE, Ke S, Kwon S, Liang F, Fan Z, Lu Y, Hirschi K, Mawad ME, Barry MA, Sevick-Muraca EM: Comparison of visible and near-infrared wavelength-excitable fluorescent dyes for molecular imaging of cancer. J Biomed Opt. 2007, 12: 024017-10.1117/1.2717137.View ArticleGoogle Scholar
  63. Tanaka E, Ohnishi S, Laurence RG, Choi HS, Humblet V, Frangioni JV: Real-time intraoperative ureteral guidance using invisible near-infrared fluorescence. J Urology. 2007, 178: 2197-2202. 10.1016/j.juro.2007.06.049.View ArticleGoogle Scholar
  64. Foster AE, Kwon S, Ke S, Lu A, Eldin K, Sevick-Muraca E, Rooney CM: In vivo fluorescent optical imaging of cytotoxic T lymphocyte migration using IRDye800CW near-infrared dye. Applied Optics. 2008, 47: 5944-5952. 10.1364/AO.47.005944.View ArticleGoogle Scholar
  65. Kovar JL, Volcheck W, Sevick-Muraca E, Simpson MA, Olive DM: Characterization and performance of a near-infrared 2-deoxyglucose optical imaging agent for mouse cancer models. Anal Biochem. 2009, 384: 254-262. 10.1016/j.ab.2008.09.050.View ArticleGoogle Scholar
  66. Wang GJ, Liu Y, Qin A, Shah SV, Deng ZB, Xiang X, Cheng Z, Liu C, Wang J, Zhang L: Thymus exosomes-like particles induce regulatory T cells. J Immunol. 2008, 181: 5242-5248.View ArticleGoogle Scholar
  67. Duysen EG, Lockridge O: Whole body and tissue imaging of the butyrylcholinesterase knockout mouse injected with near infrared dye labeled butyrylcholinesterase. Chem-Biol Interact. 2008, 175: 119-124. 10.1016/j.cbi.2008.02.011.View ArticleGoogle Scholar
  68. Tanaka E, Choi HS, Fujii H, Bawendi MG, Frangioni JV: Image-guided oncologic surgery using invisible light: Completed pre-clinical development for sentinel lymph node mapping. Ann Surg Oncol. 2006, 13: 1671-1681. 10.1245/s10434-006-9194-6.View ArticleGoogle Scholar
  69. Tucker BA, Rahirntula M, Mearow KM: A procedure for selecting and culturing subpopulations of neurons from rat dorsal root ganglia using magnetic beads. Brain Res Protoc. 2005, 16: 50-57. 10.1016/j.brainresprot.2005.10.004.View ArticleGoogle Scholar
  70. Cheng FY, Su CH, Yang YS, Yeh CS, Tsai CY, Wu CL, Wu MT, Shieh DB: Characterization of aqueous dispersions of Fe3O4 nanoparticles and their biomedical applications. Biomaterials. 2005, 26: 729-738. 10.1016/j.biomaterials.2004.03.016.View ArticleGoogle Scholar
  71. Liu SY, Long L, Yuan Z, Yin LP, Liu R: Effect and intracellular uptake of pure magnetic Fe3O4 nanoparticles in the cells and organs of lung and liver. Chinese Med J. 2009, 122: 1821-1825.Google Scholar
  72. Jain TK, Morales MA, Sahoo SK, Leslie-Pelecky DL, Labhasetwar V: Iron oxide nanoparticles for sustained delivery of anticancer agents. Mol Pharm. 2005, 2: 194-205. 10.1021/mp0500014.View ArticleGoogle Scholar
  73. Harisinghani MG, Saini S, Hahn PF, Weissleder R, Mueller PR: MR imaging of lymph nodes in patients with primary abdominal and pelvic malignancies using ultrasmall superparamagnetic iron oxide (Combidex). Acad Radiol. 1998, 5: S167-S169. 10.1016/S1076-6332(98)80095-0.View ArticleGoogle Scholar
  74. Chen Y, Dhara S, Banerjee SR, Byun Y, Pullambhatla M, Mease RC, Pomper MG: A low molecular weight PSMA-based fluorescent imaging agent for cancer. Biochem Biophys Res Commun. 2009, 390: 624-629. 10.1016/j.bbrc.2009.10.017.View ArticleGoogle Scholar
  75. Gamarra LF, Pontuschka WM, Amaro E, Costa-Filho AJ, Brito GES, Vieira ED, Carneiro SM, Escriba DM, Falleiros AMF, Salvador VL: Kinetics of elimination and distribution in blood and liver of biocompatible ferrofluids based on Fe3O4 nanoparticles: An EPR and XRF study. Mat Sci Eng C-Bio S. 2008, 28: 519-525. 10.1016/j.msec.2007.06.005.View ArticleGoogle Scholar
  76. Jain TK, Reddy MK, Morales MA, Leslie-Pelecky DL, Labhasetwar V: Biodistribution, clearance, and biocompatibility of iron oxide magnetic nanoparticles in rats. Mol Pharm. 2008, 5: 316-327. 10.1021/mp7001285.View ArticleGoogle Scholar
  77. Zhu MT, Feng WY, Wang Y, Wang B, Wang M, Ouyang H, Zhao YL, Chai ZF: Particokinetics and extrapulmonary translocation of intratracheally instilled ferric oxide nanoparticles in rats and the potential health risk assessment. Toxicol Sci. 2009, 107: 342-351. 10.1093/toxsci/kfn245.View ArticleGoogle Scholar
  78. Lacava LM, Garcia VAP, Kuckelhaus S, Azevedo RB, Sadeghiani N, Buske N, Morais PC, Lacava ZGM: Long-term retention of dextran-coated magnetite nanoparticles in the liver and spleen. J Magn Magn Mater. 2004, 272-76: 2434-2435. 10.1016/j.jmmm.2003.12.852.View ArticleGoogle Scholar
  79. Lacava LM, Azevedo RB, Bao SN, Morais PC, Lacava ZGM: Dextran-coated magnetite nanoparticles effects in mice: a transmission electron microscopy investigation. Magnetics Conference, 2005 INTERMAG Asia 2005 Digests of the IEEE International. 2005, 455-456. full_text.View ArticleGoogle Scholar
  80. Ferrucci JT, Stark DD: Iron oxide-enhanced MR imaging of the liver and spleen: review of the first 5 years. AJR Am J Roentgenol. 1990, 155: 943-950.View ArticleGoogle Scholar
  81. Gajdosikova A, Gajdosik A, Koneracka M, Zavisova V, Stvrtina S, Krchnarova V, Kopcansky P, Tomasovicova N, Stolc S, Timko M: Acute toxicity of magnetic nanoparticles in mice. Neuro Endocrinol. 2006, 27: 96-99.Google Scholar
  82. Zhai Y, Wang XL, Wang XM, Xie H, Gu HC: Acute toxicity and irritation magnetic of water-based dextran-coated magnetic fluid injected in mice. J Biomed Mater Res. 2008, 85A: 582-587. 10.1002/jbm.a.31189.View ArticleGoogle Scholar
  83. Chouly C, Pouliquen D, Lucet I, Jeune JJ, Jallet P: Development of superparamagnetic nanoparticles for MRI: Effect of particle size, charge and surface nature on biodistribution. J Microencapsul. 1996, 13: 245-255. 10.3109/02652049609026013.View ArticleGoogle Scholar
  84. Weissleder R, Heautot JF, Schaffer BK, Nossiff N, Papisov MI, Bogdanov A, Brady TJ: Mr Lymphography - Study of a High-Efficiency Lymphotrophic Agent. Radiology. 1994, 191: 225-230.View ArticleGoogle Scholar
  85. Anzai Y, Mclachlan S, Morris M, Saxton R, Lufkin RB: Dextran-Coated Superparamagnetic Iron-Oxide, an Mr Contrast Agent for Assessing Lymph-Nodes in the Head and Neck. AJNR Am J Neuroradiol. 1994, 15: 87-94.Google Scholar
  86. Okon E, Pouliquen D, Okon P, Kovaleva ZV, Stepanova TP, Lavit SG, Kudryavtsev BN, Jallet P: Biodegradation of Magnetite Dextran Nanoparticles in the Rat - a Histologic and Biophysical Study. Lab Invest. 1994, 71: 895-903.Google Scholar
  87. Briley-Saebo K, Hustvedt SA, Haldorsen A, Bjornerud A: Long-term imaging effects in rat liver after a single injection of an iron oxide nanoparticle based MR contrast agent. J Magn Reson Imaging. 2004, 20: 622-631. 10.1002/jmri.20175.View ArticleGoogle Scholar


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