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. 2015 Jul 25;5(10):1144–1153. doi: 10.7150/thno.11754

Manganese (II) Chelate Functionalized Copper Sulfide Nanoparticles for Efficient Magnetic Resonance/Photoacoustic Dual-Modal Imaging Guided Photothermal Therapy

Renfa Liu 1, Lijia Jing 1,3, Dong Peng 2, Yong Li 3, Jie Tian 2, Zhifei Dai 1,✉
PMCID: PMC4533097  PMID: 26284144

Abstract

The integration of diagnostic and therapeutic functionalities into one nanoplatform shows great promise in cancer therapy. In this research, manganese (II) chelate functionalized copper sulfide nanoparticles were successfully prepared using a facile hydrothermal method. The obtained ultrasmall nanoparticles exhibit excellent photothermal effect and photoaoustic activity. Besides, the high loading content of Mn(II) chelates makes the nanoparticles attractive T1 contrast agent in magnetic resonance imaging (MRI). In vivo photoacoustic imaging (PAI) results showed that the nanoparticles could be efficiently accumulated in tumor site in 24 h after systematic administration, which was further validated by MRI tests. The subsequent photothermal therapy of cancer in vivo was achieved without inducing any observed side effects. Therefore, the copper sulfide nanoparticles functionalized with Mn(II) chelate hold great promise as a theranostic nanomedicine for MR/PA dual-modal imaging guided photothermal therapy of cancer.

Keywords: Copper sulfide nanoparticles, Nanotheranostic agent, Photoacoustic imaging, Magnatic resonance imaging, Photothermal therapy.

Introduction

Photothermal therapy (PTT) employing near infrared (NIR) light-absorbing agents to generate heat and “boil” tumor cells has gained increasing attention for its minimal invasiveness and potential effectiveness 1, 2. A large number of NIR-absorbing nanomaterials including organic nanomaterials and inorganic nanostructures have been explored for photothermal ablation of cancer 3-7. In recent years, image-guided therapy has been developed as a new concept to achieve highly efficient and accurate treatments of cancers 2, 8. By integrating contrast enhanced medical imaging capability with therapeutic agent, the therapeutic efficiency can be greatly enhanced by monitoring the distribution of nanoparticles in real-time before, during and after the therapeutic process avoiding damage to surrounding normal tissues and cells 9, 10. Since no single imaging modality is perfect and sufficient enough to provide all aspects of anatomical and functional information, the development of multi-modal imaging guided therapy is clearly attractive 11-14.

As one of the most prominent imaging tools in daily clinics, magnetic resonance imaging (MRI) has become the preferred tool for detecting cancer owing to its excellent soft tissue contrast and unlimited penetration depth. However, the application of MRI is limited by its poor sensitivity 11, 15. Several groups have explored to combine optical imaging with MRI to compensate the innate limitations of MRI 16-18. However, these traditional optical techniques have limited spatial resolution and penetration depth 19, 20. Photoaoustic imaging (PAI) is an emerging technology that integrates both the merits of optical contrast and ultrasonic resolution 21, 22. By providing high optical contrast images at a microscale resolution and a reasonable penetration depth, PAI is expected to be a promising candidate for combination with MRI 23-25.

Superparamagnetic iron oxide (SPIO) has been a prevailing MRI contrast agent since its development for liver imaging 26. However, the inherent disadvantage of SPIO resulting from the negative contrast effect and magnetic susceptibility greatly limited its applications in MRI 27. Gadolinium (III)-based chelates are another prevailing contrast agent for clinical MRI. Unfortunately, Gd(III) based agents are reported to be possibly involved in nephrogenic system fibrosis and thus restricted for clinical use by the FDA (Food and Drug Administration)28. As an essential element for human, manganese (II) possesses strong qualities for use in MRI comparable to Gd(III) 29, while the biocompatibility of Mn(II) is much better than that of Gd(III) 30. Therefore, in recent years, increasing researches have been done to explore Mn(II) based agents for MRI 31-33.

Copper sulfide nanoparticles (CuS NPs) are promising nanomaterials for PTT developed in recent years 34, 35. Compared with the widely-explored gold nanostructures, CuS NPs are advantageous in regard to their ultrasmall size, low cost of production and unique optical properties without need for elaborate shape design 34. CuS NPs-based nanoplatforms have been studied for image guided therapy, indicating their promising future in cancer theranostics 36. Although several researches have been reported to utilize CuS NPs for PAI or MRI guided therapy 37-40, the application of CuS NPs for MR/PA dual-modal imaging guided cancer therapy through systematic administration has not yet been reported to the best of our knowledge.

Herein, a multifunctional nanoplatform based on CuS NPs functionalized with Mn(II) chelate and poly(ethylene glycol) (PEG) (CuS@MPG NPs) was developed for MR/PA dual-modal imaging guided PTT (Figure 1A&B). The CuS@MPG NPs exhibit ultrasmall size, excellent NIR-absorbing capability and minimal cytotoxicity. The high loading content of Mn(II) chelates confers the CuS@MPG NPs relatively high relaxivity, making it promising non-Gd(III) MRI contrast agent. After i.v. injection into tumor-bearing mice, the CuS@MPG NPs could be efficiently accumulated in tumor, which was demonstrated by PAI and MRI results. The tumors were then irradiated with NIR laser and photothermally ablated without any observed side effects. Our results highlight the bright future of CuS@MPG NPs as a multifunctional nanoplatform for image-guided therapy.

Figure 1.

Figure 1

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Schematic illustration of CuS@MPG NPs: (A) the structure; (B) multifunction for MR/PA dual-modal imaging guided PTT through i.v. injection.

Materials and Methods

Materials

Copper (II) chloride (CuCl2), sodium sulfide nonahydrate (Na2S·9H2O), manganese acetate tetrahydrate ((Mn(CH3COO)2·4H2O), diethylene triamine pentacetate acid (DTPA) was all obtained from Sinopharm Chemical reagent Co. LTD. Thiol-terminated methoxypoly(ethylene glycol) (mPEG-SH; molecular weight 5000 Da) was purchased from Beijing Kaizheng Biotech. Fluorescein poly(ethylene glycol) thiol (FITC-PEG-SH, molecular weight 5000 Da) was obtained from Shanghai ToYongBio. All chemicals are of analytical grade and used directly without further purification. Millipore quality deionized water (DI water) (resistivity is 18.2 MΩ·cm) was utilized in all experiments.

Preparation of NPs

0.1 mmol DTPA was dissolved in 84 mL DI water, and then 5 mL of 10 mM manganese acetate solution were added. The solution were then stirred at 55 °C for 1 h to form stable Mn(II)-DTPA. 20 mg mPEG-SH (for FITC-labeled CuS@MPG NPs, 5% mPEG-SH was replaced with FITC-PEG-SH) and 10 mL of 10 mM CuCl2 solution were added and further stirred for 5 min, followed by drop-wise addition of 1 ml of 0.1 M of Na2S. After 5 min, the reaction mixture was heated to 90 °C and stirred for 30 min until a dark-green solution was obtained. The mixture was then transferred to ice-cold water. Further dialysis was performed to exclude unreacted agents. The dialysis procedure was done against DI water with a relative sample to water volume ratio of 1: 200 for 48 hours. Water was refreshed regularly for at least eight times. After that, the samples were frozen in liquid nitrogen and lyophilized for 24 h using a SIM FD5-3 freeze drier. The powdery CuS@MPG NPs were stored at 4 °C.

PEG-stabilized CuS NPs (PEG-CuS NPs) was synthesized using previously described method 35. For Mn(II)-DTPA, 0.1 mmol DTPA was dissolved in 10 mL phosphate based solution (PBS), after which 0.1 mmol manganese acetate was added. The solution were then stirred at 55 °C for 2 h to form stable Mn(II)-DTPA. The Mn(II)-DTPA solution was stored at 4 °C before using.

Characterizations of CuS@MPG NPs

Transmission electron microscopy (TEM) and high resolution TEM (HRTEM) images of CuS@MPG NPs were obtained using a Hitachi H9000 TEM (Japan) operated at 300 kV. The hydrodynamic diameter of the CuS@MPG NPs was determined with a PALS/90Plus dynamic light scattering (DLS) analyzer (Brookhaven Instruments Co., USA). The absorption spectra of CuS@MPG NPs were recorded using an UV-vis-NIR spectrometer (Evolution 220, Thermo Scientific) using quartz cuvettes with an optical path of 1 cm. The concentration of Cu and Mn element was determined by inductively coupled plasma atomic emission spectroscopy (ICP-AES) (PROFILE SPEC, Leeman).

Photothermal Heating Experiments in Vitro

The CuS@MPG NPs and PEG-CuS NPs of various concentrations were added in quartz cuvettes (2.0 mL), irradiated by continuous-wave diode NIR laser with a center wavelength of 808 ± 10 nm and output power of 2 W for 5 min. The temperature was measured by a thermocouple inserted into the solution perpendicular to the light path every 10 s.

Cellular experiments

The photothermal ablation effect of CuS@MPG NPs to cancer cells was evaluated with the MDA-MB-231 cells. The cell line was derived from human breast cancer cells. MDA-MB-231 cells were seeded onto a 24-well plate at a density of 5 × 104 cells/well, a day before the experiment. After incubated with CuS@MPG NPs or PEG-CuS NPs, cells were then exposed to NIR laser (808 nm, 0.64W/cm2) for 10 min and stained with calcein AM (calcein acetoxymethyl ester) and PI (propidium iodide) to verify the photohyperthermic effect on cancer cells.

To determine the cellular uptake of CuS@MPG NPs, MDA-MB-231 cells pre-seeded in 12-well plates were incubated with CuS@MPG NPs for 4 h. After washing cells with PBS for 3 times, cells were stained with 40, 6-diamidino-2-phenylindole (DAPI) and then imaged by a confocal laser scanning microscope (Nikon, A1R-si).

The photothermal cytotoxicity of CuS@MPG NPs to MDA-MB-231 cells under NIR irradiation was further quantitatively investigated using the conventional 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) assay. MDA-MB-231 cells were dispensed into a 96-well flat bottom plate (1 × 104 cells/well), 1 day before the experiment. The cells were then exposed to CuS@MPG NPs or PEG-CuS NPs of various concentrations and irradiated by NIR laser (0.64 W/cm2) for 10 min and the cell viabilities were determined by the standard MTT assay according to the manufacturer suggested procedures.

PAI Procedure

All phantom and in vivo mouse imaging experiments were performed using a real-time multispectral optoacoustic tomographic (MSOT) imaging system (inVision 128, iThera Medical GmbH, Neuherberg, Germany).The phantom is made of polyurethane, specially designed to mimic the shape, size and optical properties of the mouse, containing two inner cylindrical channels for holding the control medium (PBS) and the contrast agent dissolved in PBS.

Female Balb/c nude mice were purchased from Beijing Vital River Laboratories and all animal experiments were conducted under protocols approved by Peking University Laboratory Animal Center. Xenograft mice models were established by injecting subcutaneously 5-6 × 106 MDA-MB-231 cells into the right flank of mouse. For in vivo PAI tests, MDA-MB-231 tumor-bearing mice were i.v. injected with CuS@MPG NPs (0.48mg/mouse). A volume ROI consisting of transverse slices with a step size of 0.3 mm spanning through the tumor region was selected by manual inspection of live MSOT images. Multispectral imaging was performed before injection, and 1 h, 3 h, 5 h, 8 h and 24 h after injection. Images were reconstructed using a model-based approach 41, 42.

MRI Procedure

Both in vitro and in vivo MRI tests were performed on a 7.0-T MRI system designed for small animal imaging (Bruker). T1-weighted images of CuS@MPG NPs at various concentrations in pure water were acquired using the following parameters: repetition time (TR) = 1500 ms, echo time (TE) = 7 ms. Relaxivity r1 was calculated from the slopes of relaxation time (T1) versus the concentration of Mn(II). For in vivo MRI tests, MDA-MB-231 tumor-bearing mice were treated with an i.v. injection of CuS@MPG NPs (0.48 mg/mouse) and T1-weighted images were acquired before and 24 h after injection.

Pharmacokinetic and Biodistribution Study

Wistar rats were obtained from Beijing Vital River Laboratories. To determine the circulation time, CuS@MPG NPs (0.48mg/mouse) were injected into tumor free rats via the tail vein. Blood samples (0.3 mL) were collected at the time points of 0.2, 0.5, 1, 2, 4, 8, 12, and 24 h after intravenous injection. The pharmacokinetics profile of CuS@MPG NPs in bloodstream was finally evaluated by measuring the Cu content in blood over the course of 24 h via ICP method after decomposing the blood samples by aqua regia.

For biodistribution assay, MDA-MB-231 tumor-bearing mice were sacrificed at 24 h after i.v. injection of CuS@MPG NPs (0.48mg/mouse, n = 3). Major organs including heart, liver, spleen, lung, kidney, and tumor were collected, weighed, and then solubilized by aqua regia. The concentrations of Cu and Mn in those tissue lysate samples were measured by ICP. The levels of CuS@MPG NPs in blood and various organs are presented as the percentage of injected dose per gram of tissue (%ID /g).

PTT in Vivo

MDA-MB-231 tumor-bearing mice were i.v. injected with CuS@MPG NPs solution dispersed in PBS (0.48mg/mouse). In control groups, mice were injected with the same volume of PBS. Mice with and without CuS@MPG NPs injection were irradiated with the 808 nm NIR laser at a power density of 0.64 W/cm2 for 10 min. Temperature elevation of tumor area was monitored in a real-time way with a thermometer inserted into the tumor and an infrared thermal camera (Fluke Ti27). The tumor sizes were measured by a caliper every other day and calculated as the tumor volume = (tumor length) × (tumor width)2 /2. Mice with tumor sizes exceeding 1000 mm3 were euthanatized according to the standard animal protocol. Relative tumor volumes were calculated as V/V0 (V0 was the tumor volume when the treatment was initiated). Vital organs including heart, liver, spleen, lung and kidney of mice in agent+laser group and untreated healthy mice were collected and stained using standard hematoxylin & eosin (H&E) staining protocol.

Results and discussion

Preparation and Characterization of CuS@MPG NPs

The CuS@MPG NPs were prepared using a previously reported method with some modification 38. In brief, the chelating agent of diethylene triamine pentaacetic acid (DTPA) was mixed with manganous acetate to form stable Mn(II)-DTPA, followed by addition of mPEG-SH and copper chloride. Finally, a deep-green CuS@MPG NPs solution was formed upon addition of sodium sulfide. The excess agents were removed through dialyzing against pure water for 48 h. The obtained NPs aqueous solution was then freeze-dried to powder and stored at 4 oC. The TEM images revealed that the CuS@MPG NPs displayed a rather uniform size distribution with an average size at ~ 9 nm (Figure 2A). The effective diameter of CuS@MPG NPs in water measured with DLS test was 31.8 nm (Figure S1), larger than TEM diameter. The difference between these two tests was probably due to the PEGylated modification on the surface of CuS@MPG NPs, which was invisible under TEM. HRTEM images of CuS@MPG NPs showed that the lattice spacing of (102) plane was approximately 0.30 nm (Figure 2B), in agreement with previously reported lattice spacing of (102) plane of hexagonal CuS nanostructures (0.305 nm)43. The powdery CuS@MPG NPs were quite stable and could be stored for several months without any obvious change (data not shown). The CuS@MPG NPs could be well re-dispersed in various solutions and exhibit a quite similar NIR absorption characteristics with a strong absorption peak at ~930 nm (Figure 2C&D), consistent with previously reported CuS NPs 35. Besides, the size and size distribution of CuS@MPG NPs suspended in these solutions were relatively stable without any obvious changes (Figure S1), indicating the colloidal stability of CuS@MPG NPs.

Figure 2.

Figure 2

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Characterization of CuS@MPG NPs: (A) TEM images and particle size distribution based on TEM results (Inset); (B) HRTEM images; (C) UV-vis-NIR spectra; (D) Photos of CuS@MPG NPs dispersed in water, PBS, fetal bovine serum (FBS), RMPI-1640 culture media containing 10% FBS and DMEM culture media containing 10% FBS.

Using an ICP-AES, the molar ratio of copper to manganese in CuS@MPG NPs was determined to be ~5.15. Assuming the density of CuS NPs to be 4.6 g/cm3 34, each CuS@MPG NP was estimated to contain 2140 Mn(II) ions combined with the average diameter of 9 nm. The high loading content of Mn(II) chelates is expected to confer CuS@MPG NPs ability to enhance the contrast in MRI images. We determined the longitudinal relaxivity of CuS@MPG NPs at various concentrations under a 7.0-T MRI scanner (Figure 3A&B). The relaxivity r1 was measured to be 7.10 mM-1s-1, which is a relatively high value among existing Mn(II)-based contrast agents 29. The excellent ability to shorten longitudinal relaxation times of protons from bulk water makes the CuS@MPG NP promising Mn(II)-based contrast agents for T1-weighted MRI.

Figure 3.

Figure 3

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(A) In vitro T1-weighted MRI images of CuS@MPG NPs aqueous solutions with increasing concentrations of Mn(II). (B) Linear relationship between T1 relaxation rate (1/T1) and Mn(II) concentrations in CuS@MPG NPs aqueous solutions. (C) Normalized PA signal and absorbance of CuS@MPG NPs solutions as a function of wavelength. (D) PA signal intensity as a function of optical densities (OD) at 808 nm.

The CuS NPs were reported previously as an excellent PAI contrast agent 37, 39, 40. In order to demonstrate the PA activity of CuS@MPG NPs, a phantom measurement was performed, in the 680-900 nm wavelength range, at five different concentrations using literature-described protocols 44. After image reconstruction, it was shown that the PA activity of CuS@MPG NPs was wavelength-dependent (Figure 3C). The PA spectrum exhibited a strong correlation with optical absorption spectrum. The small difference in trend between NIR absorbance and PA intensities was possibly due to light fluence changes resulting from variations in laser intensity 44. Besides, the PA signals were linearly correlated with concentrations of NPs (Figure 3D). These phantom results showed that the CuS@MPG NPs possessed good PA contrast enhanced capability.

NIR Photothermal Heating Effects

One of the most striking feature of CuS@MPG NPs is their phothermal conversion ability, which can be used for PTT of cancer. To investigate temperature elevation induced by CuS@MPG NPs in combination with NIR laser irradiation, the aqueous solution of CuS@MPG NPs with different concentrations (with same total volume of 2.0 mL) in quartz cuvettes was exposed to a continuous-wave fiber-coupled diode laser (808 nm, 2 W) for 5 min. Figure 4A showed that temperature collected by a digital thermometer every 10 s of samples under irradiation rose with increasing time. The temperature elevation of 6.4, 9.5, 10.7, 13.9 and 15.4 oC was achieved under the NIR laser irradiation of CuS@MPG NPs aqueous solution for 5 min with OD at 808 nm of 0.1, 0.2, 0.3, 0.4, 0.5, respectively (Figure 4B). On the contrary, the temperature changed only 2.3 oC when pure water was exposed to the laser, verifying the excellent photothermal activity of CuS@MPG NPs. The temperature elevation of CuS@MPG NPs is very close to that of PEG-CuS NPs with the same OD at 808 nm (Figure 4B).

Figure 4.

Figure 4

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(A) The temperature of the aqueous dispersion of CuS@MPG NPs with different concentrations changed as time. (B) Plot of temperature elevation (ΔT) of CuS@MPG NPs and PEG-CuS NPs over a period of 5 min versus OD at 808 nm. (C) In vitro cytotoxicity of CuS@MPG NPs and PEG-CuS NPs to MDA-MB-231 cells. (D) Photothermal cytotoxicity to MDA-MB-231 cells as a function of laser irradiation time and NPs concentration.

The photothermal ablation ability of CuS@MPG NPs was then evaluated at cellular level with MDA-MB-231 cells. CuS@MPG NPs could be efficiently internalized by MDA-MB-231 cells after incubation for 4 h (Figure S2), and then heat could be generated with CuS@MPG NPs upon laser irradiation to induce localized cellular death. As shown in Figure S3, cells treated with NPs plus NIR irradiation experienced substantial cellular death while no apparent cellular death was observed in cells treated with NPs or laser alone.

The standard MTT assay was then conducted to quantitatively determine the relative viabilities of MDA-MB-231 cells under various treatments. The concentration of Mn in CuS@MPG NPs solution at the OD808 nm of 0.5 was measured to be ~0.058 mM. As shown in Figure 4C & Figure S4, cell viabilities of MDA-MB-231 cells remained higher than 80% when treated with CuS@MPG NPs, bulk PEG-CuS NPs and Mn(II)-DTPA at comparable concentrations, indicating negligible cytotoxicity of CuS@MPG NPs. However, less than 20% of MDA-MB-231 cells survived when treated with CuS@MPG NPs at the OD808 nm of 0.4 under NIR irradiation (808 nm, 0.64 W cm-2) for 10 min (Figure 4D). Besides, the photothermal cytotoxicity of CuS@MPG NPs against MDA-MB-231 cells was dose-dependent similar to PEG-CuS NPs. These results demonstrated the potential of CuS@MPG NPs as a photothermal agent for localized ablation of cancer cells under NIR laser irradiation.

Dual-modal Imaging in Vivo

The ideal nano-agent for cancer therapy should be able to be efficiently accumulated in tumor site after systematic administration. Utilizing the real-time MSOT imaging system, the in vivo behavior of CuS@MPG NPs was investigated. PA images were collected before and after a single i.v. injection of CuS@MPG NPs. As shown in Figure 5A, the initial PA signal in the tumor site before injection was rather weak. But just 1 h after injection, the signal clearly showed up and gradually increased over time (Figure 5A&B). While the overall PA signal in the tumor region nearly reaches the highest in 5 h, the signals expanded throughout the region in the following time, suggesting that large amounts of CuS@MPG NPs circulated in the blood and then accumulated at the tumor site. It provided a good evidence of the high efficiency of tumor targeting of these nanoparticles. CuS@MPG NPs could be passively accumulated into tumor due to the enhanced permeation and retention (EPR) effect.

Figure 5.

Figure 5

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(A) PA images collected by MOST imaging system before (pre) and at various time points (1 h, 3 h, 5 h, 8 h, 24 h) after i.v. injection of CuS@MPG NPs. (B) PA signals in the tumor region as a function of time post-injection. (C) T1-weighted MRI images before (pre) and 24 h after i.v. injection of CuS@MPG NPs. (D) MR signals in the tumor region pre-injection and 24 h post-injection (P < 0.05, Student's t-test).

The MSOT results were further confirmed by in vivo MRI results. Utilizing the relatively high r1 relaxivity of CuS@MPG NPs, we performed in vivo MRI tests under the 7.0-T MR imaging system. As shown in Figure 5C&D, compared to images collected pre-injection, significantly enhanced T1-weighted MR signals were observed in the tumor 24 h post-injection, which was correlated with MSOT results. It suggested that the CuS@MPG NPs remained in the tumor sites as long as 24 h to provide adequate time for the following treatment. All these results demonstrated the potential of CuS@MPG NPs as MR/PA dual-modal imaging contrast agents.

In Vivo Blood Circulation and Biodistribution

The in vivo behavior of CuS@MPG NPs was also investigated using standard ICP method. As shown in Figure S5A, CuS@MPG NPs displayed a prolonged blood circulation half-time of 3.56 ± 0.43 h. The biodistribution data of CuS@MPG NPs in vivo at 24 h post-injection indicated that the highest uptake of CuS@MPG NPs was found in reticuloendothelial systems (RES) such as liver and spleen, followed by tumor (Figure S5B). The higher uptake of CuS@MPG NPs by tumor can be attributed to the EPR effect and the longer circulation time, in agreement with the in vivo imaging results. Besides, no significant difference between the biodistribution of Cu and Mn content was observed, indicating the relatively well stability of CuS@MPG NPs. Therefore, the passively targeted CuS@MPG NPs can be used to display the tumor area by MR/PA dual-modal imaging to guide the NIR laser irradiation for photothermal ablation of tumors without damaging surrounding healthy tissues.

PTT in Vivo

Both of the PAI and MRI results indicated that CuS@MPG NPs can be efficiently accumulated in the tumor site 24 h after i.v. injection, which may be the optimal time for further photothermal ablation of tumor. We then performed in vivo PPT on MDA-MB-231 tumor-bearing nude mouse xenograft models. The tumor-bearing mice were divided into four groups: control group, laser-only group, agent-only group and agent+laser group. Mice in agent-only group and agent+laser group were i.v. injected with CuS@MPG NPs (200 µL, 0.48mg/mouse), while 200 µL PBS per mouse in control group and laser-only group. After 24 h, tumors in laser-only group and agent+laser group were exposed to the NIR laser (808 nm, 0.64 W/cm2, 10 min). The temperature in tumor region was recorded in real-time with a thermometer inserted into tumor and an infrared thermal camera (Figure 6A&B). The center tumor temperature in agent+laser group reached ~54.5 °C in 10 min and remained above 50 °C for more than 6 min, obviously beyond the threshold cancer cells could tolerate. On the contrary, tumor temperature in laser-only group did not exceed 41 °C.

Figure 6.

Figure 6

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In vivo photothermal therapy using CuS@MPG NPs. (A) Temperature evolution on tumors of MDA-MB-231 tumor-bearing mice with and without CuS@MPG NPs monitored with a thermometer during laser treatment. (B) The infrared thermal images from tumor region in laser-only group and agent+laser group, respectively (808 nm laser, 0.64 W/cm2 for 10 min. The thermal images were taken in the last second of laser irradiation). (C) The tumor growth curves and (D) body weights of mice bearing MDA-MB-231 tumors after different treatments indicated (n = 5). (E) Representative photographs of mice in four groups 21 days after treatments. (F) Histological examination of vital organs (heart, liver, spleen, lung and kidney) of mice in agent+laser group at 21th day after treatments. Untreated healthy mouse was used as control. Scale bar = 50 µm.

The high tumor temperature in agent+laser group resulted in tumor growth inhibition in the following days after treatment. As shown in Figure 6C, mice tumors in agent+laser group were obviously inhibited after treatment and completely eliminated within the first week. In contrast, tumor growth in laser-only group and agent-only group was not affected compared with control group. This indicated only CuS@MPG NPs injection plus NIR irradiation were able to account for tumor inhibition, while either of them alone could not.

During our experimental process, no body weight loss or other abnormalities were observed in the four groups (Figure 6D&E), suggesting all treatments during PTT were acceptable to tumor-bearing mice. The histological examination further demonstrated biocompatibility of our treatments (Figure 6F). No noticeable abnormality including inflammation, cell necrosis and apoptosis were observed in heart, liver, spleen, lung and kidney.

These results all demonstrated the potential of CuS@MPG NPs as a theranostic agent for image-guided photothermal therapy. After systematic administration, CuS@MPG NPs firstly act as a MR/PA dual-modal contrast agent. Utilizing the synergistic advantage of MRI and PAI, the in vivo behavior of CuS@MPG NPs is monitored and the location and size of tumor are identified. After that, CuS@MPG NPs can then be applied for PTT under guidance of MR/PA dual-modal imaging results and real-time monitoring of infrared thermal imaging, resulting in greatly improved therapeutic efficiency of tumor without damaging surrounding normal tissues.

Conclusion

In summary, we have successfully prepared Mn(II) chelate functionalized copper sulfide nanoparticles for combined MR/PA dual-modal imaging-guided phototherapy. The resultant CuS@MPG NPs exhibit ultrasmall size, high photothermal conversion efficiency and minimal in vitro cytotoxicity. The in vivo MRI and PAI results indicated that the nanoparticles could be accumulated in the tumor region by EPR effect in 24 h after i.v. injection, which was further verified by ICP results. The in vivo PTT results showed that the tumors were efficiently ablated. No recurrences or side effects were observed during the experiments. Hence, our results promise the exploration of CuS NPs-based systems as theranostic nanomedicine for accurate and personalized treatment of cancer.

Supplementary Material

Supplementary Figures S1-S5.

Click here for additional data file. (1.1MB, pdf)

Acknowledgments

This work was financially supported by National Natural Science Foundation for Distinguished Young Scholars (Grant No. 81225011), State Key Program of National Natural Science of China (Grant No. 81230036), National Natural Science Foundation of China (Grant No. 21273014) and the Foundation for Innovative Research Groups of the National Natural Science Foundation of China (Grant No. 81421004).

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