Preparation and Characterization of a Tumor-Targeting Dual-Image System Based on Iron Oxide Nanoparticles Functionalized with Folic Acid and Rhodamine

1Facultad de Quı́mica, Universidad Autónoma del Estado de México, 50120 Toluca, MEX, Mexico 2Instituto Nacional de Investigaciones Nucleares, Departamento de Materiales Radiactivos, 52750 Ocoyoacac, MEX, Mexico 3Instituto de Fı́sica, Universidad Nacional Autónoma de México, 04510 Ciudad de México, Mexico 4Unidad de Investigación Biomédica en Cáncer INCan-UNAM, Instituto Nacional de Cancerologı́a, 14080 Ciudad de México, Mexico 5Centro Conjunto de Investigación en Quı́mica Sustentable UAEM-UNAM, Universidad Autónoma del Estado de México, Toluca, MEX, Mexico


Introduction
Molecular imaging comprises the noninvasive monitoring of functional and spatiotemporal processes at cellular, subcellular, or molecular levels in humans and other living systems.Although molecular imaging has existed for decades, recent advances in molecular and cell biology, imaging technology, and material sciences have greatly increased its power and potential as specific and sensitive medical tools [1].
Nanoparticles (NPs) are submicron moieties with diameters ranging from 1 to 100 nm, depending on their intended purpose, which have many novel physical and chemical properties that are not present in the atom nor the bulk counterpart, related to the dimensions and shape, as well as morphology [2,3]; NPs have been used in many different biological and medical applications as key components for imaging probe design [4][5][6][7].
Iron oxide nanoparticles (IONPs) of magnetite type (Fe 3 O 4 ) have desirable physical and biochemical characteristics (e.g., superparamagnetism, high coercivity, low Curie temperature (  ), high magnetic susceptibility, chemical stability in physiological conditions, high saturation fields, biocompatibility, and biodegradable and nontoxic nature), which make them useful in the diagnosis and treatment in the oncology field [8][9][10].
A desirable molecular imaging probe must be able to reach specific targets with high affinity, sensitivity, and suitable biodistribution properties.Nanoparticle-based molecular imaging probes can be functionalized or modified due to their high surface area-to-volume ratio, by bioactive molecules, typically through chemical coupling via amide or ester bonds in order to reach a target site.Some of the molecules used as targeting elements include small ligands, antibodies and derivatives, aptamers and other nucleic acids, polyunsaturated fatty acids, peptides, and proteins [2,[11][12][13].Furthermore, surface modification can include fluorescence dyes, genes, or drugs, to provide multimodal functionalities [3].
Folic acid (FA) is a water-soluble vitamin, can be easily conjugated to supramolecular and macromolecular structures, and has been used as a vector for cancer cells targeting due to its high affinity (  ∼ 10 −10 mM) for its corresponding folate receptors (FRs: FR  , FR  , and FR  ), to mediate cellular uptake of FA [12,[14][15][16][17][18].
FRs are overexpressed in a large number of cancer cells and are positively associated with tumor stage and histologic grade (e.g., ovarian cancer, endometrial cancer, kidney cancer, colorectal cancer, lung cancer, breast cancer, brain cancer, and myeloid leukemia); FRs provide a special marker that distinguishes cancer cells from normal cells, as these exhibit limited expression, are largely restricted to those important for embryonic development (e.g., placenta and neural tubes), and present low levels in folate resorption through kidney and lung.It has been reported that folate conjugation to the IONPs enhances the cellular uptake to target cells, improving therapeutic efficacy [12,[17][18][19][20][21].
Rhodamine B isothiocyanate, on the other hand, is a fluorophore that belongs to the xanthene dyes family.Due to its photophysical properties and excellent photostability, it is used as fluorescence probes for imaging sensor techniques.Optical imaging allows noninvasive drug visualization in cells and tissues in order to understand molecular processes in real time.Specifically, it has been reported that several MNPs (magnetic nanoparticles) can be used as dual-modality imaging probes, in nuclear and optical fluorescence imaging which is the case of IONPs [22][23][24][25].
Therefore, we aimed to develop a tumor-targeting dualimage system based on IONPs with folic acid as a vector and rhodamine isothiocyanate as an imaging agent, primarily designed for noninvasive monitoring, in order to acquire high-quality targeted images without cytotoxicity to normal cells.

Synthesis of Magnetic Iron Oxide Nanoparticles (IONPs)
and Surface Activation.Bare magnetic iron oxide nanoparticles were synthesized by an alkaline coprecipitation of Fe 3+ and Fe 2+ , in agreement with Banerji et al., [26].For surface activation, a freshly prepared aqueous solution of 2-AEP (1 mM) was added to 4 mM of a colloidal suspension of NPs with sonication using a high-intensity ultrasonic probe during an hour.Then, the resulting nanoparticle suspension was stirred vigorously at 25 ∘ C for 24 h.The particles were then washed with deionized water three times via magnetic decantation and finally dried by evaporation at 37 ∘ C. Samples were stored for posterior use (see Figure 1(a)).

Synthesis of the Iron Oxide Folate Conjugate (IONPs-FA).
Magnetic iron oxide NPs were modified with folic acid (FA) using a solution of FA (2.5 mM) in 5 mL of dichloromethane (DCM).The solution was mixed with an ethanolic solution of N-(3-dimethylaminopropyl)-  -ethylcarbodiimide (EDC) (75 mM) and 4-(dimethylamino) pyridine (DMAP) (15 mM).Afterwards, the solution was sonicated using a high-intensity ultrasound probe during 2 h.The solution was allowed to stand overnight.Posteriorly, the solution was stirred vigorously at 25 ∘ C during 24h, and the IONPs were recovered and washed via magnetic decantation, using ethanol and deionized water as diluents (see Figure 1(b)).The product was stored for use in the subsequent steps.

Synthesis of Amine-Functionalized Magnetofluorescent RITC Nanoparticles (IONPs-RITC
).An aqueous suspension of 2-AEP-functionalized INOPs (∼25 mg) was prepared and homogenized using a high-intensity ultrasound probe for 10 min.Then, RITC (0.25 mM) was dissolved in 10 mL of DMSO, and the solution of RITC was added dropwise to the aqueous suspension.Once the mixture was complete, the resulting suspension was sonicated for an hour in the dark.Nanoparticles were recovered by magnetic concentration and washed thoroughly with deionized water; samples were stored for posterior use.

Synthesis of Iron Oxide Folate Fluorescent Nanoparticles (FA-IONPs-RITC).
To create the multifunctional system, ∼1.3 mg of RITC (0.25 mM) was dissolved in 10 mL of DMSO.Then, the solution was added dropwise in the dark to the previous iron oxide folate suspension (IONPs-FA).The resulting suspension was sonicated during an hour.After that, the system was thoroughly washed with deionized water via magnetic concentration and stored for posterior use (see Figure 1(c)).200 kV in order to observe the two-dimensional relative size and morphology of nanoparticles.Samples were prepared for analysis by evaporating a drop of aqueous product on a carbon-coated TEM copper grid.At least 1000 nanoparticles were measured using the Image J software, to determine the mean diameter of nanoparticles.

X-Ray
Diffraction.X-ray diffraction (XRD) patterns of naked iron oxide cores were recorded on a powder diffractometer Bruker D8 Advance to characterize the crystallite type.Sample was concentered with magnetic decantation and dried by evaporation at room temperature and high vacuum.After that, sample was removed and desiccated thoroughly over dried silica gel and posteriorly screened with the goniometer at 2 angles from 5 ∘ to 80 ∘ at a step width of 0.03 ∘ .

Infrared Spectroscopy.
The IR spectra were acquired from vacuum-dried samples on a PerkinElmer System 2000 spectrometer with an ATR platform (Pike Technologies) by applying the Attenuated Total Reflection Fourier Transform Infrared (ATR-FTIR) spectroscopy with a 4 cm −1 resolution, 40 scans, and operating range at 4000-40 cm −1 .

UV-Vis Studies.
The absorption spectra, in the range of 200-700 nm, were obtained through a Thermo Genesys 10S spectrometer using a 1 cm quartz cuvette.

Fluorescence Spectroscopy.
The emission fluorescence spectra, in the range of 450-750 nm, were obtained through a Horiba Jobin Yvon Spectrofluorometer (Fluoromax-P) with dual excitation and emission monochromators in a wavelength range between 350 and 800 nm.Nanoparticles were measured with a  exc of 398 nm using a 1 cm cuvette.Three-/0.5-secondscans were acquired.

Determination of the Concentration of FA Conjugated over the Surface of the IONPs.
The number of FA molecules attached per nanoparticle was calculated by UV-Vis spectroscopy using different FA concentration (2.5 to 10.0 mM), as in the carbodiimide reaction described in the experimental section.The concentration was calculated using the prepared standard curve ( 2 = 0.9997, with excellent linearity from 0.0125 mM to 15 mM).The experiments were conducted in triplicate.
2.4.7.Concentration of RITC Conjugated over the Surface of the IONPs.Conjugation was determined by titration using 0.0125 mM, 0.0375 mM, and 0.0625 mM RITC, employing the synthesis method described in the experimental section.Samples were washed with purified and deionized water, and the corresponding nanoparticles were measured by UV-Vis spectroscopy, calculating the concentration using the prepared rhodamine isothiocyanate standard curve ( 2 ≥ 0.9975, with excellent linearity from 0.0033 mM to 0.0673 mM).The experiments were conducted in triplicate.

Cell Proliferation
Studies/Nanoparticle-Induced Cytotoxicity.HeLa (human cervix adenocarcinoma) cells (1 × 10 4 cells/well) were seeded onto a 96-well plate and cultured in 200 L of folate-free RPMI medium containing 10% FBS, 100 units mL −1 penicillin, 100 g mL −1 streptomycin, and 0.25 g mL −1 amphotericin B at 37 ∘ C in a humidified 5%-CO 2 /95%-air atmosphere and incubated for 24 h.The cells were treated with 20 L of different FA-IONPs-RITC nanoparticle concentrations (0.5 mg mL −1 , 0.25 mg mL −1 , 0.125 mg mL −1 , and 0.0625 mg mL −1 ) and 180 L of media culture was added and incubated for 24 h at 37 ∘ C in a humidified incubator maintained at 5% CO 2 /95% air atmosphere.Thereafter, cells were washed thoroughly with PBS to remove the noninternalized nanoparticles.Cell viability was evaluated using a crystal violet staining.Untreated cells served as 100% viable cells.
2.4.9.Cellular Uptake.Nanoparticle uptake by HeLa cells was evaluated using 5 × 10 5 cells/well seeded onto 24-well plates and cultured in a total volume of 2000 L of folatefree RPMI medium containing 10% FBS, 100 units mL −1 penicillin, 10 g mL −1 streptomycin, and 0.25 g mL −1 amphotericin B at 37 ∘ C in a humidified 5%-CO 2 /95%-air atmosphere at 37 ∘ C in a humidified incubator maintained at 5%CO 2 /95% air atmosphere.To test nanoparticle uptake via folate receptors, a group of HeLa cells were pretreated with 500 L of free folic acid (11 mg/mL) in order to saturate receptors and incubated at 37 ∘ C for 2 h.After receptor saturation, both blocked and nonblocked HeLa cells were treated with 40 L of IONPs (at a concentration of 0.25 mg mL −1 ) eluted in PBS for 3 h, posteriorly supernatants were collected and measured by UV-Vis spectroscopy at 280 nm, and absorbances were extrapolated to FA calibration curve.Uptake percentage was calculated, using the baseline as untreated cells in the same conditions.The experiment was performed in triplicate.Finally the images for the cellular uptake test were obtained with an inverted confocal microscope, consisting of an Olympus IX80 with a Plan-Neofluar 40x, AxioVert (Carl Zeiss) objective, and an AxioVision software.

FT-IR Studies
3.2.1.Iron Oxide Nanoparticles.The Far-IR and FT-IR (Mid) spectra of IONPs obtained showed the characteristic vibrations for the iron oxide material, in its magnetite phase (Figure 4(a)).For the first case (700-40 cm −1 ), the mediumintense band at 345 cm −1 is attributed to the vibration of the magnetite core.The previously mentioned band has been previously reported to be specific for Fe 3 O 4 [28].In the second case, for the medium zone (4500-400 cm −1 ), the expected vibrational bands were observed at 558 cm −1 and 3256 cm −1 .The first one corresponds to the specific Fe-O vibration of iron oxide nanoparticles, which confirms the material expected.The band at 3256 cm −1 was assigned to the -OH st vibration groups due to adsorbed water on the surface of the iron oxide nanoparticles [29,30].on the nanoparticle surface, which are necessary for the posterior functionalization.The peak for the magnetite core at 558 cm −1 shifts towards higher wavenumbers, to 570 cm −1 .Also, a significant decrease in the intensity of this band was observed, which indicates the adsorption of phosphonic acids onto the magnetite surface.

IONPs-FA System.
In the FT-IR spectrum of folateconjugated nanoparticles (Figure 4(c)), the peak in the range of 3100-3500 cm −1 was assigned to the N-H st vibration from the -NH 2 and amine NH groups from folic acid.At 1648 cm −1 , the band present is related to the carbonyl group st vibration from amide and acidic groups, which exhibits less intensity and was shifted to ∼1700 cm −1 , indicating that folic acid was successfully attached to the IONPs.The bands at 1606 cm −1 and 1548 cm −1 were assigned to the characteristic FA st vibrations (amide II and amide I, resp.), which indicate the successful conjugation to the nanoparticle surface.The presence of the new band at 1530 cm −1 was confirmed from the st vibration of the amide binding between Fe 3 O 4 -NH 2 -FA, which indicates the formation of an extra amide bond attributed to the FA attachment onto the surface of IONPs, as well as the amide bands within the FA structure.Finally, it is important to mention that the vibration from the magnetite core still appears at 548 cm −1 , which suggests that, even with the formation of the conjugate, the core does not suffer any important alteration [18].

UV-Vis Studies.
The UV-Vis spectra from the unmodified magnetite, folic acid conjugate, rhodamine conjugate, folic acid/rhodamine magnetite nanoparticles, folic acid solution, and rhodamine solution have been depicted in the Figure 5(a).The magnetite core of the system, in the range 200-700 nm of the UV-Vis spectra, showed a characteristic band around 360 nm which demonstrated a suitable synthesis.The peak at ∼280 nm was assigned to FA due to the wellknown - * transitions from the pteridine ring moiety in the FA structure [31].This UV-Vis band is present in the FA aqueous solution at 282 nm and in the IONPs-FA system at 283 nm.In the case of the FA-IONPs-RITC system, in which FA is also present, the band still appeared at 283 nm [29].
On the other hand, for the UV-Vis spectra for the same systems but focus on the RITC molecules, a band around 550 nm is present, which has been reported in previous works (536 nm for IONPs-RITC and 580 nm for FA-IONPs-RITC) [32], and although it is broad, the maximum absorption occurs in the same region.

Fluorescence Studies.
In Figure 5(b), the fluorescence emission spectra from magnetite, folic acid conjugate, rhodamine conjugate, folic acid/rhodamine magnetite nanoparticles, folic acid solution, and rhodamine solution have been depicted.
The band around 575 nm for the fluorescent emission spectra of the systems containing rhodamine (FA-IONPs-RITC and IONPs-RITC) and the one for the solution of RITC are in excellent agreement with the previously reported around 570-575 nm [33,34].The differences in the band are due to the chemical environment, and the low intensity is due to the quantity employed in the synthesis procedure (being less than 0.1% of the total system).
For the systems with FA, either FA-IONPs-RITC or IONPs-AF, the emission spectra presented a common band at 545 nm.In the case of FA-IONPs-RITC, a second band appeared at 579 nm that corresponds to the RITC molecule previously described.For the band at 545 nm, according to previous studies, FA could be present in two forms (basic and acid), due to the pteridine ring moiety.In the emission spectra, the alkaline form used to have a band between 300 and 400 nm and another band in the 230-290 nm range with higher absorption coefficients than their acid form.On the other hand, the complete molecule of FA usually presents two bands (at 255 nm and 285 nm) in its alkaline form and an overlapping of the same for the acid form, resulting in a unique band at 285 nm.Considering this and assuming that the system conjugation was carried out according to what is previously proposed, it is possible to suggest that the pteridine moiety is exposed on system surface.Thus, with the fluorescence studies, it was possible to observe a relative increment of the band at 545 nm, which corresponds to the alkaline form, indicating, in that way, the correct and suitable system conjugation.However, the magnetite core presented a lower intensity band in the same region (∼545 nm), so it is possible to suggest that, in the FA-IONPs-RITC and IONPs-RITC systems, a contribution of both compounds (IONPs and FA) existed in order to increase the intensity of the band in that wavelength.As for the IONPs-RITC system, there was no FA (with its pteridine ring moiety), which can cause the appearance of a band.

FA Conjugated over the IONPs' Surface.
In accordance with the percentages obtained from analysis, it was possible to observe that, even at the lowest initial concentration of FA,  > 95% of FA in IONPs surface was reached.Also was important the fact that the reaction had a maximal saturation point with  concentration > 5.0 mM, where the percentages were over 98%.These data results were important to optimize the quantities of FA in the final system.In Table 1, the concentrations of FA employed and the percentage of conjugation over the nanoparticle surface are shown.

RITC Conjugated over the IONPs' Surface.
The results demonstrate that, even at the lowest initial concentration of RITC,  > 95% was conjugated in IONPs surface.The saturation of the system for this specific case was reached even with the lowest initial concentration employed, where the percentages were over 96%.These data results were important to optimize the quantities of RITC in the final system.In Table 1, the RITC concentrations and the conjugation percentage are shown.
Magnetite nanoparticles were successfully prepared in accordance with previous reports using a chemical coprecipitation method in a basic medium, obtaining spheroidal forms with nanometric size [26].The amino-modified nanoparticles were used as precursor, the functionalization was carried out using a derivative of phosphonic acid that undergoes easy formation of a self-assembled, strongly organic monolayer on the nanoparticle surface, and established mechanisms are the chemisorption of 2-AEP on INOPs for the introduction of polar functional groups onto the surface [27].This coating allows further functionalization by chemical reactions [2].Several studies have reported that phosphonates and phosphates bind efficiently to the iron oxide nanoparticle surface and can be useful as potential alternatives to link fatty acids or other functional groups.Also, they have good biocompatibility and a high capacity to form strong complexes with transition metals in aqueous solution and show suitable affinity for the metal oxide surface [2,35]; additionally, a significant increase on colloidal and chemical stability was observed preventing nanoparticle oxidation processes.
Considering that colloidal stability in an aqueous and physiological medium is one of the most important issues related to the biomedical applications of nanoparticles, these polar functional groups render nanoparticles thermodynamically stable against aggregation and keep them well-dispersed in aqueous media.Furthermore, this system facilitates conjugation with a variety of molecules through sulfhydryl, carboxyl, anhydride, or imine groups, allowing easy manipulation of the surface functionality [35].
The molecular imaging techniques provide a reliable methodology to monitor and record the presence, location, and extent of diseases, although methods such as computed tomography and magnetic resonance imaging have been primary tools for cancer diagnostic, the introduction of new criteria and recommendations for the assessment of an adequate diagnostic, and measure of progression disease, promoting the development of bimodal targeted contrast agents for the detection of molecular markers with both MRI and fluorescence imaging.
In our case, the formation of magnetofluorescent nanoparticles was achieved through a covalent immobilization of rhodamine B isothiocyanate (RITC) on the particle surface, by means of a thiourea linkage through a nucleophilic addition of surface-pendent amine to isothiocyanate groups, to which primary amino groups of suitable organic molecules can be covalently linked, forming the magnetic fluorescent carrier, in this particular case [22,36].
To achieve specificity and cell receptor selectivity, the magnetite nanoparticles were functionalized with folic acid.The active-NH 2 groups present on the amino-functionalized nanoparticle surface were covalently conjugated with FA via activation of the carboxyl groups in its glutamic acid moiety by the carbodiimide method.This method may lead to the formation of two structural isomers, in which FA is linked either through the -carboxyl or through -carboxyl group of its glutamic acid moiety.However, the folate linked via carboxyl group is formed as the major isomer because it is more prone to this reaction due to its higher reactivity and retains a strong affinity towards its receptor, whereas its carboxyl derivatives are not recognized as readily [36].
The information obtained with analytical technique suggests that the conjugation of the FA at the surface of the IONPs was carried out successfully, as well as the preparation of the multifunctional system FA-IONPs-RITC.

Nanoparticle-Induced Cytotoxicity.
For the cell viability test, the IONPs exposure time was 24 h as usual.It is important to note that the highest IONPs concentration employed (0.5 mg mL −1 ) was lower than concentrations used in other studies with different cell lines but much higher than in many other works with that employed magnetite [37].According to the results shown in Figure 6(a), there was a significant difference between the lowest (0.0 mg mL −1 ) and the highest (0.5 mg mL −1 ) concentrations.Despite this, all treatments showed cell viability higher than 80%.The highest FA-IONPs-RITC concentration (0.5 mg mL −1 ) showed 82.5% of viability, which demonstrated the biocompatibility of the multifunctional system.
3.8.Cellular Uptake.The folate-conjugated nanoparticles were found to be distributed within the cytoplasm, suggesting cellular internalization through receptor-mediated endocytosis, instead of adhesion to the cell surface.This study unequivocally establishes that all the iron oxide folate nanoconjugates, developed in the course of this research, are preferentially targeted towards cancer cells and effectively internalized (63 ± 7% of internalization with respect to 43 ± 5% of the blocked group).Also, the results indicated that the system with FA could enhance the intracellular uptake of the IONPs effectively, assuming that FA works as a tumor-targeting ligand, which likely enhances receptormediated endocytosis [31].Receptor-mediated internalization of nanoparticles by FA receptor in overexpressing cancer cells was further demonstrated using an inverted confocal microscope (Olympus IX80).As was predicted from the cytotoxicity experiments, photomicrographs (taken with an Olympus IX80 inverted confocal microscope and an AxioVision software) clearly showed that cellular structures were well preserved without morphology abnormalities after nanoparticles treatment (see Figure 6(b)).
According to previous reports, a nanoparticle size between 10 and 100 nm results in systems with a size small enough to avoid the mononuclear phagocyte system (MPS) and to penetrate the capillary body cavities.Also, for medical applications, nanoparticles must conform to a size smaller than 100 nm, at which they possess unique physicochemical and pharmacokinetic characteristics are desirables [12,38].
Generally, once a tumor-targeting ligand conjugate has reached its target receptor, uptake and internalization can occur through receptor-mediated bioevents, mainly receptormediated endocytosis, but phagocytosis and pinocytosis can also contribute to internalization.After endocytosis, most but not all ligand-receptor complexes dissociate in the endosomes and the ligand eventually ends up in the lysosomes, while receptors are often recycled and transported back to the cell surface by transport vesicles [31].
The results of the internalization of magnetic nanoparticles are dependent on two factors: (I) the type of coating and (II) the nanoparticle concentration [31].In the system designed, FA demonstrated that it can promote tumor cell receptor-mediated internalization [17].
A promising diagnostic imaging methods consist in molecular targeting with exogenous fluorescent agents, employing sensitive targets to report disease and metabolism activity; FA-IONPs-RITC system provides a new class of magnetic/fluorescent nanomaterial.Additionally, fluorescent properties of this conjugate, water soluble, chemically stable, and biocompatible, are desirable features for pharmaceutical purposes.New molecular imaging devices offer the advantage for better spatial resolution and could be applied to extend three-dimensional tissue architecture and dynamic metabolic processes.The development of hybrid contrast agents is based on increasing capabilities to overcome depth tissue limitations and spatial accuracy by image fusion techniques.

Conclusions
In this work, iron oxide magnetite nanoparticles, modified with folic acid/rhodamine, were successfully synthetized via carbodiimide reaction.This system demonstrated optimal conditions for their use in medical application.The proposed uptake mechanism is through folic acid receptor endocytosis.However, to assure that such mechanism is involved, it is necessary to carry out studies focused on the labeling and tracing of the mechanism through recognition of its receptor.Also, PK studies are crucial in order to elucidate their behavior in vivo and also to prove their magnetic and fluorescent properties.

2. 4 . 1 .
Size and Morphology.Nanoparticles were analyzed by TEM in a JEOL JEM 2010 HT microscope operating at

Figure 1 :
Figure 1: Schematic synthesis of amine-functionalized magnetite nanoparticles: (a) the surface of IONPs was modified with 2-AEP to form an amine-functionalized phosphonate monolayer, and (b) folic acid/rhodamine isothiocyanate were conjugated through the carbodiimide reaction, in order to obtain FA-IONPs-RITC.
(a)).Size distribution showed a monomodal population; the frequency histogram is shown in Figure 2(b).The EDS patterns shown in (Figure 2(c)), diffraction from the samples consisting of fine particles, and the broad ring patterns from crystal planes attributed to Fe 3 O 4 nanoparticles confirm the nucleus composition.Additionally, crystallographic High Resolution TEM (HRTEM) showed the highly crystalline Fe 3 O 4 nanoparticles with the lattice fringes, corresponding to (220) and (111) planes of magnetite crystal with lattice spacing of 0.30 and 0.49 nm, respectively.
Nanoparticles.The FT-IR of 2-AEP functionalized IONPs (Figure 4(b)) showed a strong band at 1026 cm −1 from the st vibration related to the overlapping of the signals which correspond to the vibrations of M-O-P, P=O, and the P-O bond.The band at 3361 cm −1 corresponds to the -NH 2 group st vibration, which is confirmed with the bending scissoring vibration present at 1631 cm −1 .These two bands confirm the presence of the amino-terminal groups

Figure 2 :
Figure 2: (a) TEM micrograph of unmodified magnetite nanoparticles; (b) particle size distribution (PSD) histogram and adjusted fit function; (c) HRTEM of a fine particle and (d) DR pattern attributed to the diffraction from the crystal planes of Fe 3 O 4 nanoparticles.

Figure 6 :
Figure 6: (a) Effect of folate-rhodamine-conjugated nanoparticles on the HeLa cells viability.Cells incubated with different nanoparticle concentrations for 24 h at 37 ∘ C followed by crystal violet staining.* No significant reduction ( < 0.05) in cellular viability was observed, the survival rate being higher than 80%, even at the highest nanoparticle concentration.(b) Photomicrographs of cellular uptake test in HeLa cells at two different concentrations.The black arrows show the internalization of the system, which is visible even at low concentrations (0.065 mg mL −1 ).

Table 1 :
Vis spectra of unmodified magnetite, folic acid conjugate, rhodamine conjugate, folic acid/rhodamine magnetite nanoparticles, folic acid solution, and rhodamine solution.(b) Fluorescence emission spectra of magnetite, folic acid conjugate, rhodamine conjugate, folic acid/rhodamine magnetite nanoparticles, folic acid solution, and rhodamine solution.Determination of concentration of FA and RITC conjugated over the IONPs' surface.