Facile Synthesis of Fe3O4@Au/PPy-DOX Nanoplatform with Enhanced Glutathione Depletion and Controllable Drug Delivery for Enhanced Cancer Therapeutic Efficacy

The complex physiological environment and inherent self-healing function of tumors make it difficult to eliminate malignant tumors by single therapy. In order to enhance the efficacy of antitumor therapy, it is significant and challenging to realize multi-mode combination therapy by utilizing/improving the adverse factors of the tumor microenvironment (TME). In this study, a novel Fe3O4@Au/PPy nanoplatform loaded with a chemotherapy drug (DOX) and responsive to TME, near-infrared (NIR) laser and magnetic field was designed for the combination enhancement of eliminating the tumor. The Fe2+ released at the low pH in TME can react with endogenous H2O2 to induce toxic hydroxyl radicals (·OH) for chemodynamic therapy (CDT). At the same time, the generated Fe3+ could deplete overexpressed glutathione (GSH) at the tumor site to prevent reactive oxygen species (ROS) from being restored while producing Fe2+ for CDT. The designed Fe3O4@Au/PPy nanoplatform had high photothermal (PT) conversion efficiency and photodynamic therapy (PDT) performance under NIR light excitation, which can promote CDT efficiency and produce more toxic ROS. To maximize the cancer-killing efficiency, the nanoplatform can be successfully loaded with the chemotherapeutic drug DOX, which can be efficiently released under NIR excitation and induction of slight acidity at the tumor site. In addition, the nanoplatform also possessed high saturation magnetization (20 emu/g), indicating a potential magnetic targeting function. In vivo and in vitro results identified that the Fe3O4@Au/PPy-DOX nanoplatform had good biocompatibility and magnetic-targeted synergetic CDT/PDT/PTT/chemotherapy antitumor effects, which were much better than those of the corresponding mono/bi/tri-therapies. This work provides a new approach for designing intelligent TME-mediated nanoplatforms for synergistically enhancing tumor therapy.


Introduction
According to the latest estimated data from the World Health Organization's International Agency for Research on Cancer (IARC), by 2020, the number of new cancer cases worldwide has risen to 19.29 million, and the number of deaths will reach 9.96 million. Malignant tumors have become one of the serious diseases threatening human health. Recently, more and more researchers are engaged in the design of multi-mode tumor therapy and the synthesis of related materials because the use of a single modality for cancer treatment is limited. Currently, chemotherapy/photodynamic therapy chemotherapy/photodynamic therapy (CT/PDT) [1,2], PDT/photothermal therapy (PDT/PTT) [3], toxic ROS. At the same time, good photothermal conversion performance can promote CDT efficiency. In addition, to maximize the cancer-killing efficiency, the nanoplatform can be successfully loaded with the chemotherapeutic drug DOX, which can be efficiently released under NIR excitation and induction of slight acidity at the tumor site. Both in vitro cell experiments and in vivo tumor-bearing mouse experiments confirmed the nanoplatform's synergistic multimodal antitumor effect. In conclusion, the proposed TME-mediated Fe3O4@Au/PPy nanoplatform represents a new and versatile approach for the development of smart nanomedicines in the field of cancer therapy. Scheme 1. Illustration of the fabrication of the Fe3O4@Au/PPy nanoplatform.

Synthesis of Fe3O4@Au/PPy Nanocomposites
Magnetic Fe3O4 NPs were prepared according to our previously reported method [37]. First, 1.35 g of FeCl3•6H2O was dispersed in 40 mL of ethylene glycol and stirred until it became homogeneous and clear. Then, 3.6 g of NaAc and 1.0 g of polyethylene glycol were added. The mixed solution was stirred vigorously for 30 min and then transferred to a 50 mL Teflon reactor. It was heated at 200 °C for 5 h and cooled naturally to room temperature. Black Fe3O4 products were recovered and separated by magnet, washed with ultra-pure water and anhydrous ethanol several times, and dried for 8 h at 60 °C.
Au NPs were synthesized as reported previously [38]. After 0.25 mL of HAuCl4 solution (0.01 M) was accurately measured, 9.75 mL of CTAB (0.1 M) and 0.6 mL of NaBH4 (0.01 M) were mixed with it. The above mixed solution was stirred for 2 min and allowed to stand for 2 h.
The 300 mg of Fe3O4 was added to 70 mL of DI water and stirred for 15 min to form a dispersion. Subsequently, 15 mL of ethanol solution containing 3 mL of pyrrole was added to the Fe3O4 dispersion and ultrasonically stirred for 20 min. After that, 15 mL of HCl aqueous solution (6 M) and 10 mL of the obtained Au NPs solution were mixed into the above suspension and ultrasonically stirred for 1.5 h. The black solid obtained by magnet was dispersed in 70 mL of H2SO4 aqueous solution (0.5 M), with ultrasonic stirring for 4 h. The black suspension was filtered, and the precipitate was washed and dried to obtain the black product, which was labeled as Fe3O4@Au/PPy. The preparation of Fe3O4@PPy was similar to that of Fe3O4@Au/PPy except for the addition of Au NPs.

Synthesis of Fe 3 O 4 @Au/PPy Nanocomposites
Magnetic Fe 3 O 4 NPs were prepared according to our previously reported method [37]. First, 1.35 g of FeCl 3 ·6H 2 O was dispersed in 40 mL of ethylene glycol and stirred until it became homogeneous and clear. Then, 3.6 g of NaAc and 1.0 g of polyethylene glycol were added. The mixed solution was stirred vigorously for 30 min and then transferred to a 50 mL Teflon reactor. It was heated at 200 • C for 5 h and cooled naturally to room temperature. Black Fe 3 O 4 products were recovered and separated by magnet, washed with ultra-pure water and anhydrous ethanol several times, and dried for 8 h at 60 • C.
Au NPs were synthesized as reported previously [38]. After 0.25 mL of HAuCl 4 solution (0.01 M) was accurately measured, 9.75 mL of CTAB (0.1 M) and 0.6 mL of NaBH 4 (0.01 M) were mixed with it. The above mixed solution was stirred for 2 min and allowed to stand for 2 h.
The 300 mg of Fe 3 O 4 was added to 70 mL of DI water and stirred for 15 min to form a dispersion. Subsequently, 15 mL of ethanol solution containing 3 mL of pyrrole was added to the Fe 3 O 4 dispersion and ultrasonically stirred for 20 min. After that, 15 mL of HCl aqueous solution (6 M) and 10 mL of the obtained Au NPs solution were mixed into the above suspension and ultrasonically stirred for 1.5 h. The black solid obtained by magnet was dispersed in 70 mL of H 2 SO 4 aqueous solution (0.5 M), with ultrasonic stirring for 4 h. The black suspension was filtered, and the precipitate was washed and dried to obtain the black product, which was labeled as Fe 3 O 4 @Au/PPy. The preparation of Fe 3 O 4 @PPy was similar to that of Fe 3 O 4 @Au/PPy except for the addition of Au NPs.

Photothermal Performance
In order to investigate the photothermal effect, Fe 3 O 4 @PPy or Fe 3 O 4 @Au/PPy nanocomposites with different concentrations (0.1, 0.2 and 0.3 mg/mL) were prepared. The 1 mL dispersion was added to the sample bottle, and the temperature change under the irradiation of 808 nm laser (1 W/cm 2 ) was recorded by Fluke Ti32 thermal infrared camera.

Detection of ROS
1,3-Diphenylisobenzofuran (DPBF) was used as a molecular probe to detect ROS production. Typically, 20 mL of DPBF (0.09 mM) was mixed with 1 mL of sample dispersion (300 µg/mL), and the absorbance of DPBF in the solution at 410 nm was measured after 808 nm laser the irradiation at different times. To determine the PDT effect of PPy, we etched the Fe 3 O 4 @PPy with HCl (PPy-Etch) and detected the ROS induced by PPy-Etch.

Consumption of GSH and Generation of OH
After 0.0024 g of Fe 3 O 4 @Au/PPy nanocomposites was added into 5 mL of GSH solution (200 µmol/L) dissolved in N,N-dimethylformamide (DMF) solution, 250 µL of o-diphenanthrene solution (100 mmol/L) was added. After stirring for 15 min, the pH of the solution was adjusted to 5.5. The absorbance was measured every hour at a wavelength of 512 nm.
After 0.0028 g of Fe 3 O 4 @Au/PPy nanocomposites was added into 5 mL of GSH solution (200 µmol/L) dissolved in DMF solution, 100 µL of H 2 O 2 (100 mmol/L) and 0.7 mL of methylene blue (MB) solutions (100 mmol/L) were added and stirred for 15 min. The pH of the solution was adjusted to 5.5. The absorbance at 660 nm was measured every hour at a wavelength of 660 nm.

DOX Loading and Release
In a typical experiment, Fe 3 O 4 @Au/PPy-DOX nanocomposites were prepared by mixing DOX·HCl (at various weights: 1, 3, 5, 10 and 20 mg) in 5 mL of phosphate buffer solution (PBS) with 10 mg Fe 3 O 4 @Au/PPy. The mixture was placed in a dark shaker overnight. Excess DOX was removed by centrifugation, and the precipitate was washed with PBS several times [39][40][41][42][43]. A UV-Vis spectrophotometer was used to measure the absorbance of the collected solution, and the DOX loading on the nanocomposites was calculated by Formula (1) [37,[44][45][46]: Loading rate = amount of added drug − amount of drug in supermatant amount of added drug * 100% (1) In the laser-triggered drug release tests, Fe 3 O 4 @Au/PPy-DOX nanocomposites were added into PBS solution at pH 5.0 and 7.4 under 37 • C and irradiated by the 808 nm laser (0.75 W/cm 2 ) for different durations. The changes in absorbance of DOX at 490 nm were recorded by UV-Vis spectra. All the tests were performed in triplicate, and the average values were taken to calculate the release ratio of DOX from Fe 3 O 4 @Au/PPy-DOX with time using Formula (2): Loading rate = amount of released drug amount of loaded drug * 100% (2)

Cell Experiments
The in vitro cytotoxicities of samples were investigated by MTT assay. Firstly, the prepared nanocomposites (1 mg/mL) were dispersed in incubation medium and then diluted to different concentrations (1, 10, 100 µg/mL). HeLa cells were seeded in 96-well plates at a concentration of 5 × 10 4 cells per well and cultured for 24 h (5% CO 2 , 37 • C) to allow the cells to attach. After removing the incubation medium, 100 µL aliquots of fresh culture medium containing different concentrations of nanocomposites were added to the wells, which were incubated for 4 h. Then, the irradiation groups were exposed to an 808 nm NIR laser at 1 W/cm 2 for 10 min under the same culture conditions. After all groups were incubated for another 20 h, the cell viability was determined by MTT assay.
To further study the cytotoxicity of the nanocomposites toward HeLa cells, Hoechst 33342 and PI were used to observe the cell-killing situation. Firstly, HeLa cells were seeded in 6-well plates with a density of 5 × 10 4 cells per well; after adherence, they were incubated with 1 mg/mL of Fe 3 O 4 @Au/PPy or Fe 3 O 4 @Au/PPy-DOX with or without a magnetic field for about 0.5 h. For phototherapy, corresponding culture dishes were further incubated for 1 h followed by exposure to NIR laser light at 808 nm for 10 min. After irradiation, the HeLa cells were incubated again for 12 h (5% CO 2 , 37 • C), followed by washing with PBS (pH = 7.4) to remove the culture medium and staining with 0.5 mL of Hoechst 33342 (1 µg/mL) or PI (1 µg/mL) for 10 min under darkness. The viable cells or necrotic cells could be identified by intact nuclei dyed with Hoechst 33342 or PI, respectively. Dual fluorescence-stained culture media were washed, and the cells were observed and imaged using an inverted fluorescence microscope. All experiments were performed in triplicate.

Animal Models
Mice were obtained from the Laboratory Animal Center of Anhui Medical University (Certification of Quality 34000200000077, 34000200000078). This study was conducted in strict accordance with the recommendations in the Regulations on the Management of Laboratory Animals in China promulgated in 1988. All the animal experiments were in agreement with the guidelines of the Animal Experiments and Care Regulations of Anhui University and approved by the Animal Use Committee of Anhui University. @Au/PPy-DOX+L. Each group was treated with different samples which were injected via tail vein at the dose of 5-6 mg/kg (sample/mouse weight) and then exposed to different external conditions. Afterward, the mice were weighed and the tumor sizes were measured by a caliper every day; the tumor volume was calculated by Formula (3), and the tumor inhibition rate was calculated by Formula (4):

In Vivo Synergistic Antitumor Effect
where a and b mean the maximum length (mm) and minimum width (mm) of the tumor, respectively. After the treatment of 18 days, all the mice were sacrificed, the tumor of each mouse was collected and cleaned and digital photos of tumors were obtained using a camera.

Results and Discussion
A novel self-sacrificial template route was proposed for the synthesis of Fe 3 O 4 @Au/PPy nanocomposites, and Fe 3 O 4 and Fe 3 O 4 @PPy were also successfully synthesized for the control experiment. Figure 1 shows the microstructure and phase composition of Fe 3 O 4 , Fe 3 O 4 @PPy and Fe 3 O 4 @Au/PPy NPs. A typical scanning electron microscope (SEM) image ( Figure 1A) and a typical transmission electron microscopy (TEM) image ( Figure 1D) indicated that the obtained Fe 3 O 4 NPs exhibited a uniform spherical shape with a diameter of about 150 nm. Fe 3 O 4 @PPy and Fe 3 O 4 @Au/PPy nanocomposites also had uniform sphere-like structures with diameters larger than Fe 3 O 4 NPs, which may be attributed to the successful capping of PPy on the surface of Fe 3 O 4 NPs ( Figure 1B,C). It can be determined from Figure 1E that the Fe 3 O 4 core was covered with a PPy layer with a thickness of about 10 nm, which presented a clear core-shell structure. As shown in Figure 1F, Au NPs were inserted into the PPy shell. The HRTEM images of Fe 3 O 4 @Au/PPy nanocomposites ( Figure 1G) indicated a lattice spacing of 0.48 nm, which is attributed to the (110) plane of Fe 3 O 4 , demonstrating the presence of a Fe 3 O 4 core. After Au NPs were added in the synthesis process, a small number of black spots could be observed in the PPy shell layer in the TEM image ( Figure 1F), suggesting the existence of Au NPs and the successful preparation of Fe 3 O 4 @Au/PPy nanocomposites. When high-resolution transmission electron microscopy (HRTEM) images of the shell region were taken, lattice fringes of 4.80 and 2.90 Å were observed, which corresponded to the (110) planes of Fe 3 O 4 and the (111) plane of Au, respectively. Subsequently, the composition and crystalline structure of the products were characterized by X-ray diffraction (XRD) patterns ( Figure 1I). In Figure 1I-a, there is only a broad peak located at 2θ of 20-30 • , which implies that pure PPy was amorphous [34]. Due to the presence of Fe, the magnetic hysteresis loops of Fe3O4 NPs and Fe3O4@Au/PPy nanocomposites were investigated by applying an external magnetic field. As shown in Figure 2A, the saturation magnetization of Fe3O4 NPs was 68 emu/g, while that of Fe3O4@Au/PPy nanocomposites was 20 emu/g. Weakening of the magnetization of nanocomposites may be ascribed to the presence of the non-magnetic PPy shell and embedded Au NPs. The illustration at the top left of Figure 2A exhibits that the nanocomposites in water were attracted toward the external magnetic field, revealing the prominent magnetic property of the Fe3O4@Au/PPy nanocomposites. The hysteresis loop diagram of the Fe3O4@Au/PPy nanocomposite in the low magnetic field region ( Figure S1, in the Supporting Materials) demonstrates the ferromagnetic state. The above results indicated Fe3O4@Au/PPy nanocomposites have good application prospects for magnetic-targeted drug delivery. Figure 2B shows the UV-Vis-NIR spectroscopy results exhibiting the optical property of the resultant Fe3O4@Au/PPy. The visible-to-NIR region had an intense and broad absorption band, and three absorption peaks of the Due to the presence of Fe, the magnetic hysteresis loops of Fe 3 O 4 NPs and Fe 3 O 4 @Au/PPy nanocomposites were investigated by applying an external magnetic field. As shown in Figure 2A, the saturation magnetization of Fe 3 O 4 NPs was 68 emu/g, while that of Fe 3 O 4 @Au/PPy nanocomposites was 20 emu/g. Weakening of the magnetization of nanocomposites may be ascribed to the presence of the non-magnetic PPy shell and embedded Au NPs. The illustration at the top left of Figure 2A exhibits that the nanocomposites in water were attracted toward the external magnetic field, revealing the prominent magnetic property of the Fe 3 O 4 @Au/PPy nanocomposites. The hysteresis loop diagram of the Fe 3 O 4 @Au/PPy nanocomposite in the low magnetic field region ( Figure S1, in the Supporting Materials) demonstrates the ferromagnetic state. The above results indicated Fe 3 O 4 @Au/PPy nanocomposites have good application prospects for magnetic-targeted drug delivery. Figure 2B shows the UV-Vis-NIR spectroscopy results exhibiting the optical property of the resultant Fe 3 O 4 @Au/PPy. The visible-to-NIR region had an intense and broad absorption band, and three absorption peaks of the nanocomposites appeared at around 510 nm, 802 nm and 1000 nm, which may have resulted from the polaron and bipolaron band transitions for PPy and the plasmon resonance absorption of Au [37], indicating that the nanocomposites could be used for photothermal therapy by transforming the absorbing NIR light energy into heat.
These results illustrated that the combination of PPy and Au NPs could achieve a synergistic effect for photothermal therapy.
The photodynamic effects of Fe3O4@PPy, PPy-Etch and Fe3O4@Au/PPy were investigated by using DPBF as an indicator. The measured peaks of DPBF solutions at 410 nm over different samples with or without NIR light are presented in Figure 2D. For all samples, the absorption peak intensity at 410 nm was weakened after irradiation, showing all three samples had a PDT effect. Compared with Fe3O4@PPy and PPy-Etch, it was found that not only the PPy but also Fe3O4 NPs could have a PDT effect after irradiation with an 808 nm laser for 10 min. After 10 min of irradiation, the PDT effect of Fe3O4@Au/PPy with embedded Au NPs was significantly enhanced compared to Fe3O4@PPy, which was attributed to the fluorescence resonance energy transfer (FRET) process between Au NPs and PPy. Au NPs could absorb the NIR light efficiently because of the surface plasmon resonance (SPR) effect [47] and transfer the absorbed light energy to PPy for generating more ROS. The above results showed that the Fe3O4@Au/PPy nanocomposites can be used as an effective photodynamic agent for inducing the generation of ROS and killing tumor cells. As we know, Fe3O4 in the prepared nanocomposite could produce Fe 3+ ions in the slightly acidic environment of tumors. Then Fe 3+ ions can be converted to Fe 2+ ions with expressed GSH on the tumor cell membrane (Chemical Equation (1)). The o-diphenanthrene can react with Fe 2+ ions to form a complex and exhibit a characteristic absorption peak at 512 nm. Therefore, the consumption of GSH and generation of Fe 2+ ions were verified by UV-Vis spectroscopy. As seen in Figure 3A, the absorbance of the mixed solution at 512 nm gradually increases with time, indicating that Fe 3+ ions played  Figure 2C shows the photothermal curves of DI water, Fe 3 O 4 @PPy and Fe 3 O 4 @Au/PPy aqueous dispersions with different concentrations under NIR irradiation from 0 to 10 min. It can be clearly observed that Fe 3 O 4 @Au/PPy nanocomposites had a better photothermal effect than Fe 3 O 4 @PPy at the same concentration, indicating the presence of Au NPs enhanced the photothermal efficiency. In addition, the concentration of Fe 3 O 4 @Au/PPy was positively correlated with the photothermal effect. The temperature enhancement of Fe 3 O 4 @Au/PPy nanocomposite dispersion (300 µg/mL) could reach about 22.5 • C after 10 min of irradiation. The photothermal impact of the products was further vividly demonstrated by the thermal images (inset of Figure 2C). These results illustrated that the combination of PPy and Au NPs could achieve a synergistic effect for photothermal therapy.
The photodynamic effects of Fe 3 O 4 @PPy, PPy-Etch and Fe 3 O 4 @Au/PPy were investigated by using DPBF as an indicator. The measured peaks of DPBF solutions at 410 nm over different samples with or without NIR light are presented in Figure 2D. For all samples, the absorption peak intensity at 410 nm was weakened after irradiation, showing all three samples had a PDT effect. Compared with Fe 3 O 4 @PPy and PPy-Etch, it was found that not only the PPy but also Fe 3 O 4 NPs could have a PDT effect after irradiation with an 808 nm laser for 10 min. After 10 min of irradiation, the PDT effect of Fe 3 O 4 @Au/PPy with embedded Au NPs was significantly enhanced compared to Fe 3 O 4 @PPy, which was attributed to the fluorescence resonance energy transfer (FRET) process between Au NPs and PPy. Au NPs could absorb the NIR light efficiently because of the surface plasmon resonance (SPR) effect [47] and transfer the absorbed light energy to PPy for generating more ROS. The above results showed that the Fe 3 O 4 @Au/PPy nanocomposites can be used as an effective photodynamic agent for inducing the generation of ROS and killing tumor cells.
As we know, Fe 3 O 4 in the prepared nanocomposite could produce Fe 3+ ions in the slightly acidic environment of tumors. Then Fe 3+ ions can be converted to Fe 2+ ions with expressed GSH on the tumor cell membrane (Chemical Equation (5)). The o-diphenanthrene can react with Fe 2+ ions to form a complex and exhibit a characteristic absorption peak at 512 nm. Therefore, the consumption of GSH and generation of Fe 2+ ions were verified by UV-Vis spectroscopy. As seen in Figure 3A, the absorbance of the mixed solution at 512 nm gradually increases with time, indicating that Fe 3+ ions played important roles in the oxidation of GSH and the effective release of Fe 2+ ions. Thus, GSH was consumed in large quantities, effectively promoting the photodynamic effect. Fe 3+ + GSH → Fe 2+ + GSSG (1) In addition, Fe 2+ ions generated under acidic conditions and from the GSH consumption can further react with H2O2 to produce ·OH through the Fenton reaction to achieve CDT (Chemical Equation (2)). The generation of ·OH was confirmed by the degradation of methylene blue (MB). As shown in Figure 3B, MB was almost completely degraded in the Fe3O4@Au/PPy dispersion after a reaction of 9 h. Therefore, we can conclude that Fe3O4@Au/PPy not only has multiple responses to the tumor environment, such as weak acid, endogenous hydrogen peroxide and GSH, but also regulates and improves the tumor microenvironment. These results indicated that Fe3O4@Au/PPy nanocomposites can induce the formation of ·OH to realize CDT, as well as promote PDT and CDT effects by consuming GSH, thus exerting a synergistic antitumor effect. Fe3O4@Au/PPy nanoplatform not only had the multifunctional effects of PTT, CDT and PDT, but its PPy shell also offered the possibility of loading drugs. The anticancer drug DOX was loaded into the Fe3O4@Au/PPy nanoplatform and its drug release behavior was recorded. Figure 4A shows the UV-Vis absorption spectrum of Fe3O4@Au/PPy-DOX; the characteristic peak at 490 nm can be attributed to DOX, indicating the successful loading. With the increasing proportion of DOX to Fe3O4@Au/PPy, the intensity of the DOX characteristic peak was gradually enhanced. The strength was greatest when the weight ratio was 2:1. The results were consistent with the quantitative analysis shown in Figure 4B. It can be clearly seen that the loading efficiency of DOX shows an upward trend with the addition of DOX, and the saturation loading rate was about 11%, which was not objective compared with other literature [22,23]. Subsequently, the release behavior of Fe3O4@Au/PPy-DOX at different pH values was tracked, as shown in Figure 4C. It can be found that the release rate of DOX was 69% at pH 5.0, while the release rate was 47% at pH 7.4. This may be due to protonation of the amino group in DOX, which provided DOX with a positive charge and facilitated drug release at acidic pH. Furthermore, by controlling the switch of NIR, a slow and controlled DOX release behavior of the Fe3O4@Au/PPy-DOX nanoplatform can be achieved. According to Figure 4D, the cumulative DOX release amount of the Fe3O4@Au/PPy-DOX nanoplatform increased rapidly each time under NIR laser irradiation. The results showed that the release process of NIR light may be due to the loose PPy shell caused by the rapid rise in local temperature. Notably, drug release was more significant at acidic pH 5.0, while DOX release was limited at acidic pH 7.4. This special property provided the basis for the specific release of DOX in the acidic environment of the tumor. In addition, Fe 2+ ions generated under acidic conditions and from the GSH consumption can further react with H 2 O 2 to produce ·OH through the Fenton reaction to achieve CDT (Chemical Equation (6)). The generation of ·OH was confirmed by the degradation of methylene blue (MB). As shown in Figure 3B, MB was almost completely degraded in the Fe 3 O 4 @Au/PPy dispersion after a reaction of 9 h. Therefore, we can conclude that Fe 3 O 4 @Au/PPy not only has multiple responses to the tumor environment, such as weak acid, endogenous hydrogen peroxide and GSH, but also regulates and improves the tumor microenvironment. These results indicated that Fe 3 O 4 @Au/PPy nanocomposites can induce the formation of ·OH to realize CDT, as well as promote PDT and CDT effects by consuming GSH, thus exerting a synergistic antitumor effect.
Fe 3 O 4 @Au/PPy nanoplatform not only had the multifunctional effects of PTT, CDT and PDT, but its PPy shell also offered the possibility of loading drugs. The anticancer drug DOX was loaded into the Fe 3 O 4 @Au/PPy nanoplatform and its drug release behavior was recorded. Figure 4A shows the UV-Vis absorption spectrum of Fe 3 O 4 @Au/PPy-DOX; the characteristic peak at 490 nm can be attributed to DOX, indicating the successful loading. With the increasing proportion of DOX to Fe 3 O 4 @Au/PPy, the intensity of the Molecules 2022, 27, 4003 9 of 14 DOX characteristic peak was gradually enhanced. The strength was greatest when the weight ratio was 2:1. The results were consistent with the quantitative analysis shown in Figure 4B. It can be clearly seen that the loading efficiency of DOX shows an upward trend with the addition of DOX, and the saturation loading rate was about 11%, which was not objective compared with other literature [22,23]. Subsequently, the release behavior of Fe 3 O 4 @Au/PPy-DOX at different pH values was tracked, as shown in Figure 4C. It can be found that the release rate of DOX was 69% at pH 5.0, while the release rate was 47% at pH 7.4. This may be due to protonation of the amino group in DOX, which provided DOX with a positive charge and facilitated drug release at acidic pH. Furthermore, by controlling the switch of NIR, a slow and controlled DOX release behavior of the Fe 3 O 4 @Au/PPy-DOX nanoplatform can be achieved. According to Figure 4D, the cumulative DOX release amount of the Fe 3 O 4 @Au/PPy-DOX nanoplatform increased rapidly each time under NIR laser irradiation. The results showed that the release process of NIR light may be due to the loose PPy shell caused by the rapid rise in local temperature. Notably, drug release was more significant at acidic pH 5.0, while DOX release was limited at acidic pH 7.4. This special property provided the basis for the specific release of DOX in the acidic environment of the tumor.   Figure 5A,B.
Based on the excellent properties of the Fe3O4@Au/PPy-DOX nanoplatform, it was expected to become a novel anticancer agent. The relative viability of HeLa cells and different concentrations of Fe3O4@PPy, Fe3O4@Au/PPy and Fe3O4@Au/PPy-DOX after incubation under and without laser irradiation were measured by the MTT method. As expected from Figure 5A, Fe3O4@PPy and Fe3O4@Au/PPy exhibited a negligible cytotoxicity, even at 1 mg/mL. The co-presence of Fe3O4@Au/PPy and 808 nm laser irradiation reduced cell viability, suggesting that the generated heat and ROS of Fe3O4@Au/PPy under the NIR laser irradiation could efficiently kill tumor cells ( Figure  5B). In contrast, with the laser irradiation, the viability of cells incubated with Fe3O4@Au/PPy-DOX was lower (35%), indicating the synergetic anticancer effect from Fe3O4@Au/PPy as well as the anticancer drug DOX. cytotoxicity, even at 1 mg/mL. The co-presence of Fe3O4@Au/PPy and 808 nm laser irradiation reduced cell viability, suggesting that the generated heat and ROS of Fe3O4@Au/PPy under the NIR laser irradiation could efficiently kill tumor cells ( Figure  5B). In contrast, with the laser irradiation, the viability of cells incubated with Fe3O4@Au/PPy-DOX was lower (35%), indicating the synergetic anticancer effect from Fe3O4@Au/PPy as well as the anticancer drug DOX.  Figure 6B,D, the death of HeLa cells incubated with Fe 3 O 4 @PPy or Fe 3 O 4 @Au/PPy in the absence of irradiation was almost not observed (essentially no red fluorescence) owing to the good biocompatibility and low cytotoxicity of these two nanoparticles. However, when HeLa cells were cultured with Fe 3 O 4 @PPy or Fe 3 O 4 @Au/PPy with laser irradiation ( Figure 6C,E), the fluorescence image showed a merge of red and purple, revealing the killing effects of HeLa cells by PDT and PTT from nanocomposites. As shown in Figure 6F, the cells cultured with Fe 3 O 4 @Au/PPy-DOX without laser irradiation were partially killed, which may be due to the slightly acidic environment of tumor cells leading to a partial release of DOX. Strong red fluorescence could be seen after irradiation of HeLa cells cultured with Fe 3 O 4 @Au/PPy-DOX ( Figure 6G), indicating that Fe 3 O 4 @Au/PPy-DOX had an obvious antitumor effect of CT combined with multiple treatments under the excitation of NIR light, which was consistent with the MTT results. Fluorescence images were used to further demonstrate the antitumor effect of Fe3O4@PPy, Fe3O4@Au/PPy and Fe3O4@Au/PPy-DOX in vitro. As shown in Figure 6B,D, the death of HeLa cells incubated with Fe3O4@PPy or Fe3O4@Au/PPy in the absence of irradiation was almost not observed (essentially no red fluorescence) owing to the good biocompatibility and low cytotoxicity of these two nanoparticles. However, when HeLa cells were cultured with Fe3O4@PPy or Fe3O4@Au/PPy with laser irradiation ( Figure  6C,E), the fluorescence image showed a merge of red and purple, revealing the killing effects of HeLa cells by PDT and PTT from nanocomposites. As shown in Figure 6F, the cells cultured with Fe3O4@Au/PPy-DOX without laser irradiation were partially killed, which may be due to the slightly acidic environment of tumor cells leading to a partial release of DOX. Strong red fluorescence could be seen after irradiation of HeLa cells cultured with Fe3O4@Au/PPy-DOX ( Figure 6G), indicating that Fe3O4@Au/PPy-DOX had an obvious antitumor effect of CT combined with multiple treatments under the excitation of NIR light, which was consistent with the MTT results. Although Fe3O4@Au/PPy-DOX had a good therapeutic effect in vitro, its therapeutic effect in vivo also deserved to be further explored ( Figure 7A). We selected H22 tumor-bearing mice as a model and randomly divided them into nine groups: (1) PBS, (2) DOX, (3) DOX+L, (4) Fe3O4@PPy, (5) Fe3O4@PPy+L, (6) Fe3O4@Au/PPy, (7) Fe3O4@Au/PPy+L, (8) Fe3O4@Au/PPy-DOX and (9) Fe3O4@Au/PPy-DOX+L. Figure 7B shows the tumor volume changes of H22 tumor-bearing mice after different treatments. Compared with other groups, the group of Fe3O4@Au/PPy-DOX with light irradiation was found to exhibit the best suppression, which demonstrated the excellent synergistic antitumor effect of Fe3O4@Au/PPy-DOX under NIR light. The body weight of each treatment group increased slightly as a result of the normal feeding process ( Figure S2). Although Fe 3 O 4 @Au/PPy-DOX had a good therapeutic effect in vitro, its therapeutic effect in vivo also deserved to be further explored ( Figure 7A). We selected H22 tumorbearing mice as a model and randomly divided them into nine groups: (1) PBS, (2) DOX,  Figure 7B shows the tumor volume changes of H22 tumor-bearing mice after different treatments. Compared with other groups, the group of Fe 3 O 4 @Au/PPy-DOX with light irradiation was found to exhibit the best suppression, which demonstrated the excellent synergistic antitumor effect of Fe 3 O 4 @Au/PPy-DOX under NIR light. The body weight of each treatment group increased slightly as a result of the normal feeding process ( Figure S2). Overall, there was no significant difference in body weight in each group after treatment, indicating that the prepared samples had high therapeutic biosafety. The excellent antitumor effect was further proved by Figure 7C-E. In Figure 7C, we can observe that the Fe 3 O 4 @Au/PPy-DOX group possessed an outstanding ability to inhibit tumor growth under NIR light; the tumor inhibition rate could reach up to 91% ( Figure 7D). The digital photo in Figure 7E intuitively shows the size of each group of tumors. Compared with other groups, the tumor growth of H22 tumor-bearing mice injected with Fe 3 O 4 @Au/PPy-DOX with light irradiation was significantly inhibited. The in vivo experiment vividly certified that Fe 3 O 4 @Au/PPy-DOX could serve as a preferred nanomaterial for trimodal antitumor therapy. These in vivo experiments vividly demonstrated that Fe 3 O 4 @Au/PPy-DOX may be an excellent antitumor nanoagent combined with multiple therapeutic approaches under the action of NIR light and the tumor microenvironment.

Conclusions
In summary, in this work, a magnetic-targeted Fe3O4@Au/PPy-DOX nanoplatform with TME-mediated and NIR-excited multimodel tumor therapy was developed by following a sacrificial template strategy. When Fe3O4@Au/PPy-DOX is aggregated at the tumor site, it can produce heat and ROS under NIR light for PTT and PDT. Under the stimulation of the acidic environment and GSH overexpression in a tumor,

Conclusions
In summary, in this work, a magnetic-targeted Fe 3 O 4 @Au/PPy-DOX nanoplatform with TME-mediated and NIR-excited multimodel tumor therapy was developed by following a sacrificial template strategy. When Fe 3 O 4 @Au/PPy-DOX is aggregated at the tumor site, it can produce heat and ROS under NIR light for PTT and PDT. Under the stimulation of the acidic environment and GSH overexpression in a tumor, Fe 3 O 4 @Au/PPy-DOX can release Fe 3+ to catalyze the overexpressed H 2 O 2 to generate ·OH through the Fenton reaction, which can be used to realize CDT and increase ROS production. Simultaneously, the low-pH environment of the tumor can jointly trigger the release of DOX in the nanoplatform to achieve an effective synergistic antitumor therapy. It was confirmed that this work will provide distinctive horizons for the development of more novel multifunctional antitumor nanoplatforms. Meanwhile, nanoplatforms with more triggering mechanisms and more DOX capacity are expected to be investigated in the future.
Supplementary Materials: The following supporting information can be downloaded at: https://www. mdpi.com/article/10.3390/molecules27134003/s1, Figure S1: The enlarged version of Figure 2A in the region of low magnetic field.
Author Contributions: Conceptualization, C.Q. and Y.S.; Data curation, P.W. and B.G.; Formal analysis, W.W.; Investigation, H.C. and X.W.; Methodology, A.X. All authors have read and agreed to the published version of the manuscript.