A core-shell nanomaterial with endogenous therapeutic and diagnostic functions
© Springer-Verlag 2010
Received: 1 February 2010
Accepted: 13 April 2010
Published: 5 May 2010
In the present communication, we report the fabrication of a unique core-shell inorganic nanomaterial with potential therapeutic and diagnostic functions. It contains an iron–cobalt (FeCo) core that demonstrates magnetic resonance imaging (MRI) contrast property and a thin nanoshell of gold that inhibits the function of a pro-angiogenic growth factor, VEGF165. Au(FeCo) core-shell nanomaterials are fabricated in the gas phase and characterized using transmission electron microscopy, energy dispersive spectrum, inductively coupled plasma analysis, and MRI. Inhibition of VEGF165 function by Au(FeCo) is demonstrated against VEGF165/VPF-induced signaling cascades and proliferation of human umbilical vein endothelial cells (HUVECs). The self-contrast property of Au(FeCo) is determined in vitro by MRI after incubating HUVECs with Au(FeCo), demonstrating intrinsic contrast property of this potentially therapeutic nanomaterial. In brief, we report here the successful fabrication of an inorganic core-shell nanomaterial with potential therapeutic and diagnostic functions. It inhibits the function of VEGF165 and functions as a MRI contrast agent.
KeywordsNanoparticle Core-shell Angiogenesis Gold Diagnostics Therapeutics
It is recognized that nanotechnology has the potential to play an important role in human health care including angiogenesis (Gannon et al. 2008; Goldstein et al. 1995; Goodman et al. 2004; Han et al. 2007; Hong et al. 2006; Liu et al. 2007; Paciotti et al. 2004; Patra et al. 2008a; Patra et al. 2008b; Shaw et al. 2008; Sokolov et al. 2003; Sullivan and Ferrari 2004). Vascular endothelial growth factor 165 (VEGF165) plays a major role in angiogenesis by engaging VEGFR2 on endothelial cells, turning on a number of signaling cascades leading to endothelial cell proliferation, migration, survival, etc. (Ferrara and Kerbel 2005; Folkman 2007; Folkman and Hanahan 1991; Dvorak et al. 1999). Anti-angiogenic agents presently used in the clinics exhibit serious toxicities (Bhattacharya et al. 2004; Bhattacharya et al. 2007; Mukherjee et al. 2007; Mukherjee et al. 2005). Furthermore, monitoring the effect of anti-angiogenic therapy is also a challenge. Thus, there is a clear need to discover new anti-angiogenic molecules that will exhibit low toxicity and monitor the effect of the anti-angiogenic therapy by self-contrast. Here, we report the fabrication of a unique core-shell inorganic nanomaterial with such an endogenous therapeutic and diagnostic function. It contains an iron–cobalt (FeCo) core that demonstrates magnetic resonance imaging (MRI) contrast property and a thin nanoshell of gold that inhibits the function of a pro-angiogenic growth factor, VEGF165. It is also important to consider the possible toxic effects of this nanomaterial. Since the nanoparticles are in a core-shell structure, only gold is exposed to the cells or any outside environment, and FeCo alloy is prevented from contacting anything else but gold. It is general agreement that gold is noncytotoxic based on a range of studies about modified gold nanoparticles.
Au(FeCo) core-shell nanomaterials are fabricated in the gas phase and characterized using transmission electron microscopy (TEM), energy dispersive spectrum (EDS), inductively coupled plasma-mass spectrometry (ICP-MS) analysis. Inhibition of VEGF165 function by Au(FeCo) was demonstrated against VEGF165/VPF-induced signaling cascades and proliferation of human umbilical vein endothelial cells (HUVECs). Challenging the VEGF165 function in the presence of Au(FeCo) demonstrates the inhibition of VEGF165/VPF-induced proliferation of HUVECs and inhibition of phosphorylation of VEGF receptor 2 (VEGFR2) by this nanomaterial in a dose-dependent manner. However, FeCo alone, without a gold nanoshell, does not inhibit the VEGF165/VPF-induced proliferation of HUVECs nor does it inhibit the VEGF165/VPF-induced VEGFR2 phosphorylation. In the absence of VEGF165/VPF, either Au(FeCo) or FeCo did not affect the HUVEC proliferation, suggesting the non-toxic behavior of this nanocomposite material. In addition, the self-contrast property of Au(FeCo) was determined in vitro by MRI after incubating HUVECs with Au(FeCo), demonstrating the significant contrast behavior of the cells upon nanomaterial treatment compared to non-treated control cells or phospate-buffered saline (PBS). Furthermore, intracellular uptake studies determined by ICP demonstrate a dose-dependent uptake and contrast behavior of Au(FeCo). In brief, we report here the successful fabrication of an inorganic core-shell nanomaterial with potential therapeutic and diagnostic functions. It inhibits the function of VEGF165 and functions as a MRI contrast agent. The potential biomedical applications of this nanomaterial are enormous. In addition, the presence of a gold nanoshell endows flexibility to this material to surface modification for a wide variety of biological applications including targeting.
2.1 Synthesis and characterization of Au(FeCo) and FeCo nanoparticles
The FeCo–Au core-shell nanoparticles were synthesized directly in gas phase by a novel “snapshot synthesis” method (Xu and Wang 2007, 2008). The experimental apparatus consisted of a sputtering–gas–condensation source and a deposition chamber. A Fe:Co:Au (35:15:50) composite target was used to synthesize the FeCo–Au core-shell nanoparticles. The vapor of a mixture of Fe, Co, and Au atoms was generated by sputtering process. The atoms were cooled down by the collisions between the atoms and inert gas molecules, which then nucleate and grow into nanoparticles. The core-shell structure was formed by segregating the Au to the surface of the nanoparticles through heat-assisted diffusion during synthesis. The formed nanoparticles were carried out of the source by the gas flow and collected in the deposition chamber. Polyethylene glycol (PEG)-coated glass substrates were used to collect the nanoparticles and transfer them into a solution (H2O). Cu grids covered with amorphous carbon were used for the preparation of TEM samples.
The core-shell structure of FeCo–Au nanoparticles was confirmed by EDS line scan on a single nanoparticle. FeCo-Au nanoparticles were directly deposited on amorphous carbon covered Cu grids. Analysis was done under STEM mode on a field emission gun TEM (FEI Tecnai G2 F30) equipped with an EDS detector. Electron beam scanned across a single FeCo–Au nanoparticle by 1 nm step in the designated direction. A distribution spectrum of Fe, Co, and Au in a nanoparticle was obtained.
2.2 [3H]thymidine incorporation experiments
Proliferation experiments using [3H]thymidine incorporation were performed as described previously (Mukherjee et al. 2005). In brief, serum-starved HUVECs were treated with VEGF165 (10 ng/mL) either free or conjugated to different doses of Au(FeCo) or FeCo. After 24 h, cells were treated with 1 μCi of thymidine for 4 h, followed by washing in PBS, fixing the cells in cold methanol, and lysing the cells with 0.1 N NaOH. The cell lysates were read in a scintillation counter for thymidine incorporation.
2.3 Western blot analysis of VEGFR2 phosphorylation
Effect of Au(FeCo) and (FeCo) on VEGFR2 phosphorylation. Western blot analysis of phospho-VEGFR2 (p-VEGFR2) and total VEGFR2 from (1) control untreated HUVECs ,(2) A, serum-starved HUVECs were stimulated for 5 min withVEGF (10 ng/mL) as a positive control, (3–5) HUVECs treated with VEGF165 while conjugated to Au(FeCo) or (FeCo) at various concentrations [3 = 100 ng, 4 = 1 µg, and 5 = 10 µg of Fe–Co–Au], and (6–8) HUVECs treated with Fe–Co at various concentrations [6 = 100 ng, 7 = 1 µg, and 8 = 10 µg of Fe–Co]. Afterwards, the incubation cells were lysed with RIPA buffer containing PIC and halt. Cell lysates were isolated and Western blot analysis run according to literature procedure (Mukherjee et al. 2005).
2.4 Intracellular uptake of Au(FeCo)
HUVECs were grown in 100-mm collagen-coated tissue culture plates in triplicates in EGM medium and treated with different doses of (FeCo)Au for 2 h. Afterwards, the incubation cells were washed extensively in PBS thrice. Finally, the cells were trypsinized, pooled together, thoroughly washed in PBS again, and finally resuspended in PBS for ICP analysis for gold.
2.5 Magnetic resonance imaging
Samples were evaluated on 1.5 and 3 T clinical systems (GE Twin Speed EXCITE, GE Healthcare, Waukeshau, WI). Samples contained in 1-ml microcentrifuge tubes were placed in a styrofoam tube holder which was then positioned in the center of a birdcage head coil. Following three-plane single-shot fast spin echo localizing sequences, T2* and R2* measurements were performed using a multi-echo gradient echo sequence. Eight echo times (TEs) were acquired, with the following sequence parameters: TR (repetition time) 150 ms, TE 2.6–33.8 ms, flip angle 20, bandwidth 50 kHz, slice thickness of 5 mm, field of view 14 cm, imaging matrix × 256 × 160, two signals averaged. An axial slice was acquired through the bottom of the sample tubes.
Calculation of T2* and R2* was performed using Cine Tool software installed on a GE Advantage Windows 4.3 workstation (GE Healthcare, Waukeshau, WI). A region of interest (ROI) encompassing the bottom of the sample tube was placed on the image with the shortest TE and then copied to the remaining seven images with progressively longer TEs. The average signal intensity of each ROI was then measured and plotted versus TE, and the resulting data were fit to the expected single exponential decay curve describing the loss of transverse magnetization in the sample to solve for T2* and R2* (S = S0e -TE/T2* + S1, where S = signal intensity in arbitrary units, S0 and S1 are constants, and TE is the echo time. R2*, the relaxivity, is the inverse of T2*).
3 Results and discussion
To further confirm whether the inhibition of HUVEC proliferation was due to inhibition of VEGF165 function by Au(FeCo), we investigated the downstream signaling events induced by VEGF165. It is established that VEGF165 engages VEGFRs on endothelial cells leading to receptor dimerization and subsequently receptor phosphorylation at different tyrosine residues.(Mukherjee et al. 2005) Therefore, we wanted to test whether treatment of HUVECs with Au(FeCo) and FeCo had any effect on VEGFR2 phosphorylation (details are in the “Section 2”). VEGF165-induced phosphorylation of VEGFR2 was significantly inhibited when HUVECs were treated with 100 ng–10 μg of Au(FeCo) (Fig. 3c). However, under similar conditions, same doses of FeCo had no significant effect on VEGFR2 phosphorylation, further confirming our observation obtained from HUVEC proliferation experiments. The inhibition of VEGFR2 phosphorylation suggests that Au(FeCo) directly binds to VEGF165 and inhibits its function, leading to abrogation of receptor phosphorylation. These results are in agreement with our previous reports on the anti-angiogenic property of gold nanoparticles (Bhattacharya et al. 2004; Mukherjee et al. 2005; Bhattacharya and Mukherjee 2008). However, we do not rule out the possibility of the involvement of other mechanisms as well that will be investigated in the future.
After confirming the inhibition of VEGF165 function by Au(FeCo), we wanted next to determine the imaging property of this nanomaterial. We resorted to MRI technique as FeCo has the highest saturation magnetization. Cells are treated with different doses of Au(FeCo) and fixed in formalin before imaging.
FeCo cores of Au(FeCo) nanoparticles induce local magnetic field inhomogeneities which in turn cause a significant reduction in T2* (Rad et al. 2007; Bai and Wang 2005). This, in turn, means that samples with smaller values of T2* (or longer values of R2*) reflecting higher concentrations of iron will show more rapid signal decay on images with successively longer TEs. While many factors affect the intrinsic tissue relaxation times, the presence of iron typically represents the dominant contribution, and therefore measurements of T2* or R2* (relaxivity, or the inverse of T2*) can be related to the tissue concentration of iron (Alustiza et al. 2004). It may be noted that T2* does not decrease as much and its nearly reaching a plateau around 32 μg/ml may be due to the saturation uptake of the nanomaterial by the HUVECs. This is further confirmed by quantifying intracellular uptake of the core-shell materials in HUVECs by ICP analysis in terms of gold content. Figure 4b describes the dose-dependent uptake of the core-shell nanomaterials in terms of gold. The figure clearly demonstrates that the intracellular uptake reaches a plateau between 16 and 32 μg/ml of the core-shell nanomaterial (∼6–12 μg/ml in terms of Au). Thus, there is no further significant decrease in T2* beyond these points.
Taken together, the results confirm that the core-shell nanoparticles presented in this report are intrinsically multifunctional. Our results demonstrate the fabrication of Au (FeCo), a core-shell inorganic nanoparticle, containing potential therapeutic as well as diagnostic functions. Au(FeCo) inhibits the function of pro-angiogenic VEGF165 and hence inhibits VEGF165-induced proliferation of HUVECs and inhibits VEGFR2 phosphorylation. In vitro imaging by MRI confirms the self-contrast behavior of this nanomaterial and demonstrates the significant relaxation of the cells when treated with Au(FeCo) compared to control cells and PBS. To the best of our knowledge, this nanoparticle represents the first example of an inorganic nanoparticle with endogenous dual functionality. Thus, this nanomaterial can be used as a diagnostic as well as a therapeutic agent. In the future, this theranostic material may be utilized not only for the therapeutic and diagnostic application of angiogenesis-dependent disorders but may also help to monitor the effect of the treatment on the disease outcome.
This work is supported by STATE-1 (MEDICA), CA135011, CA136494 grant to PM. This work is also supported by National Science Foundation BME 0730825, NSF NNIN program, the Medical Device Center of Institute of Engineering in Medicine and Center for Nanostructures Application at University of Minnesota and Minnesota Mayo Nanotechnology Partnership for JPW.
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