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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptNIH Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
Angew Chem Int Ed Engl. Author manuscript; available in PMC May 9, 2012.
Published in final edited form as:
PMCID: PMC3334859
NIHMSID: NIHMS370002

Highly magnetic core-shell nanoparticles with unique magnetization mechanism**

Tae-Jong Yoon, Dr., Prof.,1,#+ Hakho Lee, Dr., Prof.,1,+ Huilin Shao,1 and Ralph Weissleder, Dr., Prof.1,2

Magnetic nanoparticles (MNPs) with high magnetic moments and very small size are under active development, since such materials have growing uses in biotechnology and medicine.[1] Ferromagnetic metals, rather than their corresponding oxides, have been suggested as an ideal constituent for MNPs for their superior magnetization.[2] Unfortunately, monometallic MNPs typically require protective layers to prevent progressive oxidation. To date, however, most core/shell approaches have yielded sub-optimal magnetization, as the shell was formed either by artificially oxidizing the core[3,4] or by coating it with non-magnetic materials.[5]

Here we present an approach to preparing highly magnetic, monometallic MNPs for biomedical use. The particles consisted of an elemental iron (Fe) core and an artificial ferrite-shell (Fe@MFe2O4, M = Fe, Mn, Co). The Fe cores were enlarged into a thermally stable ferromagnetic state to increase the overall magnetization. Subsequently, protective ferrite shells were grown onto the cores and metal-doped to further enhance magnetization. The resultant particles displayed a unique magnetic feature, the presence of hysteresis with negligible coercivity. Further analysis revealed a novel magnetization process wherein the shell effectively reduces the coercivity of the ferromagnetic cores by leading the magnetization process at small magnetic fields. The resulting MNPs attain high saturation magnetization but with negligible remanence to prevent inter-particle aggregations. The utility of the particles was demonstrated through the highly sensitive detection of proteins in the pico-molar ranges and of single cancer cells. The mechanism and MNP featured here could serve as a new strategy in preparing stable, highly magnetic and yet dispersible nanoparticles from ferromagnetic crystals.

We formed Fe MNPs by thermally decomposing metal complexes [Fe(CO)5] in the presence of oleylamine (OY) under air-free conditions (see Methods in Supporting Information; SI). As previously reported,[4,6] larger Fe MNPs could be obtained by lowering the molar ratio of Fe and OY ([Fe]:[OY]). The resulting particles, however, had irregular sizes and spontaneously aggregated with decreasing OY concentrations (Figure S1). The optimal value of [Fe]:[OY] for mono-dispersed particles was ~12:1, which limited the particle diameter (d) < 8 nm. To overcome this problem, we explored a new approach for increasing the particle size. Based on the rationale that higher reactivity of the decomposed iron would lead to larger particles,[7] we elevated the reaction temperature. Indeed, it was possible to fine-tune the particle size through temperature control (Figure 1a and Figure S2). Furthermore, by fixing [Fe]:[OY] = 12:1, all Fe MNPs were highly soluble and mono-disperse with relative size variations of < 5% (Figure S2).

Figure 1
New synthesis of Fe@ferrite MNPs. a) Transmission electron microscope (TEM) images of a single Fe MNP prepared at different reaction temperatures. The oxide shell was formed while transferring the particles for imaging. b) Fe MNPs were rapidly oxidized ...

When exposed to air, Fe MNPs were rapidly oxidized to form a natural iron-oxide shell (Fe@FeO; Figure 1b). The shell had an amorphous structure as confirmed by electron diffraction (Figure 1b, inset) and X-ray diffraction (XRD; Figure 1d). The saturation magnetization (Ms) of the shell, estimated using shell-only particles (Figure S2), was minimal (8 emu·g−1[Fe]). After adjusting for the shell portion, the Ms of the Fe-core was measured at ~206 emu·g−1 [Fe], which is close to that of bulk Fe (210 emu·g−1 [Fe]). The overall Ms for Fe@FeO MNPs, however, was relatively small (92 emu·g−1 [Fe]) due to the small portion of Fe-core. Moreover, the Ms degraded over time (Figure 1e) as the cores were progressively oxidized (Figure S3).

To prevent the core from oxidation, we next coated the as-synthesized Fe MNPs with protective shells. Ferrite was selected as the shell material to further enhance the overall Ms of the particles. Figure 1c shows an example of Fe MNPs encased in Fe3O4 (Fe@Fe3O4). After synthesizing Fe MNPs, we added Fe-oleate complexes and annealed the mixture at elevated temperatures to initiate ferrite formation. The crystallinity of the shell, characterized by XRD, gradually improved with increasing annealing temperature; and after aging at 300 °C for 1 hour, the diffraction pattern matched that of the spinel ferrite structure (Figure 1d). The ferrite shell was polycrystalline presumably to relieve geometrical strain (Figure S4). The relative variation of the overall particle size, however, was maintained at < 7%.

This approach offers several advantages to improve the magnetic properties of Fe MNPs. First, the ferrite shell protects the Fe-core from oxidation. The Ms of the ferrite-coated Fe MNPs were far more stable, reaching a steady value over time (Figure 1e). Second, the ferrite shell could be coated over existing Fe MNPs. Transmission electron microscope (TEM) analysis showed that the size of the Fe-core in Fe@Fe3O4 was similar to that of the initial diameter of the Fe MNPs (dotted circles in Figures 1c and 1b, respectively). Compared to an alternative method, which oxidizes the surface of Fe MNPs to form a ferrite shell[3; 4], the new approach resulted in larger Fe-cores and thereby higher Ms per particle. Third, the shell composition could be changed to tailor the magnetic property of the particles. For example, by co-injecting Mn-oleate or Co-oleate complexes with Fe-oleate ([M]:[Fe] = 1:2; M = Mn, Co), we could obtain Fe@MnFe2O4 or Fe@CoFe2O4 MNPs (Figure S4). The CoFe2O4 shells rendered the particles magnetically hard; whereas the highly magnetic MnFe2O4 shells made Fe@MnFe2O4 assume the highest Ms among Fe-core MNPs.

The prepared Fe@MFe2O4 MNPs (M = Fe, Mn, Co) were made water-soluble by coating their surface with dimercaptosuccinic acid (DMSA). The DMSA-treated MNPs did not elicit acute cytotoxicity when tested at diagnostic concentrations on cancer (HCT116, colon) or on normal (3T3, fibroblast) cells (Figure S5). To render the particles target specific, we conjugated affinity ligands (e.g., biotin, antibody) to the particle surface. The number of antibodies per particle was ~10, and the hydrodynamic diameter was ~42 nm after conjugation. Note that DMSA coating induced a negative zeta potential on the particles, enhancing the colloidal stability (see Table S1 for details).

Figure 2a shows Ms of Fe@MFe2O4 MNPs (d = 16 nm), measured at 2 hours after synthesis. For comparative analysis, ferrite MNPs with different compositions were also synthesized (Figure S6). All types of Fe@MFe2O4 MNPs had larger Ms than the ferrite ones, with Fe@MnFe2O4 assuming the largest Ms. The ferrite shells on Fe@MFe2O4 were found to have reduced magnetization compared to bulk material, presumably because of the polycrystalline nature of the shell (Table S2). Zero-field-cooled (ZFC) and field-cooled (FC) magnetization (Figure 2b) of Fe@MFe2O4 MNPs all displayed peaks at two different temperatures (TB1 > TB2), denoting the separate onset of superparamagnetism in the Fe core (TB1) and the ferrite shell (TB2).[8] The association of TB1 to the Fe-core was further confirmed by similar measurements with smaller Fe-core MNPs, which showed the shift of TB1 toward a lower temperature. Note that TB1 was ≈ 290 K with 16 nm Fe@MFe2O4 which indicated the stable, ferromagnetic nature of the Fe-core at room temperature.

Figure 2
Magnetic properties of Fe@ferrite MNPs. a) All Fe@MFe2O4 MNPs (d = 16 nm) had higher Ms than similarly-sized ferrite MNPs. Among the Fe@MFe2O4 MNPs, the overall Ms was within the same order of magnitude as the shell magnetization. b) Temperature-dependent ...

The hysteresis loops of Fe@MFe2O4 displayed an unusual feature for MNPs: negligible remanence but the presence of hysteresis loss (Figure 2c and Figure S7). For further analysis, the magnetization of Fe@MFe2O4 MNPs were calculated using an extended Stoner-Wohlfarth model, which includes the effects of non-zero temperature and cubic magnetocrystalline anisotropy (Figure S8).[9] The simulated magnetization curve showed an excellent agreement with the experimental data (Figure S9), and revealed a novel, cooperative magnetization mechanism. In Fe@MFe2O4 MNPs, the shell magnetization (Mshell) followed a typical superparamagnetic curve, whereas the core portion (Mcore) assumed stable single-domain behavior with non-zero coercivity (Hc = 350 Oe; Figure S9). The total magnetization of a particle (Mtot), which is the volume-weighted average of Mcore and Mshell, however, displayed considerably less coercivity (Hc = 40 Oe): the superparamagnetic contribution (from the Mshell) rapidly saturated to overwhelm the relatively slow magnetization of the core at low magnetic fields. The core contribution (Mcore) then became dominant at higher magnetic fields to increase the Mtot. Note that this unique property rendered the particles both highly magnetic and yet soluble in media.

To evaluate the utility of Fe@MFe2O4 MNPs for MR-based sensing, we investigated their transverse relaxivity (r2), the capacity of MNPs to shorten the transverse relaxation time (T2). Figure 3a shows the r2 values of Fe@MFe2O4 MNPs along with those of ferrite particles (see Table S3 for details). In general, the r2 rose with increasing particle size (d), as can be seen among ferrite MNPs. At the fixed size (d = 16 nm), the r2 values were proportional to Ms. Correspondingly, Fe@MFe2O4 MNPs had higher r2 than similarly-sized ferrite particles with Fe@MnFe2O4 assuming the highest value (7×10−14 L·s−1 per particle; 430 s−1·mM−1 [metal]). When analyzed with an outer-sphere model,[10] the observed r2 values were highly compatible with theoretical predictions, which validated our approach for enhancing r2, by increasing both d and Ms. A comparative study of phantoms (Figure 3b) also confirmed the superiority of Fe@MnFe2O4 as a MR contrast agent; compared to the widely-used CLIO (cross-linked iron-oxide), Fe@MnFe2O4 was able to produce the same signal changes at ~10 times lower doses. The same trend was observed in the preliminary in vivo imaging (Figure S10).

Figure 3
Characterization of transverse relaxivity. a) The transverse relaxivity (r2) of various MNPs was measured at the fixed Larmor frequency (f0 = 20 MHz; B0 = 0.47 T) and mapped as a function of both the particle size (d) and the magnetization (M) at 0.47 ...

To demonstrate the biological applications of Fe@MFe2O4 MNPs, we used the particles to sense biological markers with the NMR-based diagnostic platform (DMR, diagnostic magnetic resonance).[11] DMR sensing is based on the change of T2T2) when detection targets in samples are recognized by MNPs. We first performed molecular detection, using biotin-avidin interaction as a model system. When avidin was added to the solution of biotinylated MNPs, the particles were cross-linked to form nanometer-scale clusters, causing avidin dose-dependent ΔT2. [11] Among the other types of MNPs, Fe@MnFe2O4 showed the highest sensitivity by detecting ~1.5 pM of avidin (Methods in SI); the DMR assay thus could be as sensitive as ELISA but with the added advantage of requiring much smaller samples (~1 µL) and shorter assay times (< 30 min).

For cellular detection, we tagged human cancer cells (SkBr3) with MNPs conjugated with HER2/neu antibodies. All conjugated MNPs (Fe@MnFe2O4, Fe3O4, CLIO) showed a similar ligand density and a hydrodynamic size (Table S1). Human cells were incubated with MNPs at saturating particle concentrations (50 µg·ml−1 [metal]) and for a short time (10 min at 37 °C). These conditions were previously shown to minimize nonspecific MNP binding.[12] Following MNP-incubation and removal of unbound MNPs, the T2 values at different cell concentrations were measured and the cellular relaxivities, defined as the relaxation rate (R2 = 1/T2) per cell concentration, were obtained (Figure 4b).[12] With the limited numbers of binding sites per cell, cellular relaxivities were found to be in the same order of the particle r2, with Fe@MnFe2O4 assuming the highest value (4×10−3 µL·s−1). Host cells (leukocytes) similarly incubated with HER2/neu-specific Fe@MnFe2O4, however, showed ~103-fold lower cellular relaxivity (5×10−6 µL·s−1), confirming highly selective cell-labeling. We next prepared artificial clinical samples by spiking human cancer cells (SkBr3) into human whole blood with erythrocyte lysed, and labeled the samples with HER2/neu-specific MNPs. DMR measurements confirmed the superiority of Fe@MnFe2O4, enabling the detection of ~10 cancer cells in the presence of abundant host cells (Figure 4c).

Figure 4
Biological applications of Fe@MFe2O4 MNPs. a) The detection of small molecules was demonstrated using biotinylated MNPs. Upon the addition of avidin, biotinylated MNPs aggregated, changing the T2 of samples. Fe@MnFe2O4 MNPs showed the best detection threshold ...

In summary, we have developed a synthetic process for iron-core and ferrite-shell MNPs, wherein we achieved high magnetization by increasing the core size and modifying the shell composition. Most important, the novel magnetization of the particles provided a new insight into implementing highly magnetic nanoparticles; ferromagnetic cores can be enlarged to enhance the overall magnetic moments, while superparamagnetic shells can retain the core coercivity to prevent inter-particle aggregations. The resulting MNPs assumed high magnetic moments and commensurately high transverse relaxivities, which was utilized in MR-based diagnostics. The particles can also benefit other applications, such as bio-separation (e.g., proteins, cells) and the direct detection of biological targets using magnetometers.

Experimental Section

Details on the experimental method are available in Supporting Information online.

Footnotes

**The authors thank C. Ross (MIT) for his generous support in magnetic measurements; R. Zhang, G. Wojtkiewicz, J. Figueiredo, J. Chen and M. Nahrendorf for their assistance in MRI; N. Sergeyev for synthesizing CLIO; D. Issadore, M. Liong and E. Keliher for their helpful discussions; Y. Fisher-Jeffes for reviewing the manuscript. This work was supported in part by National Institute of Health Grants 2R01-EB004626, U54-CA119349, and TPEN contract (HHSN268201000044C).

Supporting information for this article is available on the WWW under http://www.angewandte.org or from the author.

References

1. a) Kim J, Piao Y, Hyeon T. Chem. Soc. Rev. 2009;38:372–390. [PubMed]b) Jun YW, Seo JW, Cheon J. Acc. Chem. Res. 2008;41:179–189. [PubMed]
2. a) Huber D. Small. 2005;1:482–501. [PubMed]b) Qiang Y, Antony J, Sharma A, Nutting J, Sikes D, Meyer D. J. Nanopart. Res. 2006;8:489–496.
3. Lee H, Yoon TJ, Weissleder R. Angew. Chem. Int. Ed. Engl. 2009;48:5657–5660. [PMC free article] [PubMed]
4. Peng S, Wang C, Xie J, Sun S. J. Am. Chem. Soc. 2006;128:10676–10677. [PubMed]
5. a) Ban Z, Barnakov YA, Li F, Golub VO, O'Connor CJ. J. Mater. Chem. 2005;15:4660–4662.b) Cheng J, Ni X, Zheng H, Li B, Zhang X, Zhang D. Mater. Res. Bull. 2006;41:1424–1429.
6. Shao HP, Lee H, Huang YQ, Ko IY, Kim C. IEEE Trans. Magn. 2005;41:3388–3390.
7. Park J, An K, Hwang Y, Park J, Noh H, Kim J, Park J, Hwang N, Hyeon T. Nature Mater. 2004;3:891–895. [PubMed]
8. Farrell D, Majetich SA, Wilcoxon JP. J. Phys. Chem. B. 2003;107:11022–11030.
9. Joffe I, H.R Philos. Mag. 1974;29:1051–1059.
10. Roch A, Muller RN, Gillis P. J. Chem. Phys. 1999;110:5403–5411.
11. Lee H, Sun E, Ham D, Weissleder R. Nat. Med. 2008;14:869–874. [PMC free article] [PubMed]
12. Lee H, Yoon TJ, Figueiredo J, Swirski F, Weissleder R. Proc. Natl. Acad. Sci. USA. 2009;106:12459–12464. [PMC free article] [PubMed]
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