Magnetic-Field-Induced Improvement of Photothermal Sterilization Performance by Fe3O4@SiO2@Au/PDA Nanochains

Due to the abuse of antibiotics, the sensitivity of patients to antibiotics is gradually reduced. This work develops a Fe3O4@SiO2@Au/PDA nanochain which shows an interesting magnetic-field-induced improvement of its photothermal antibacterial property. First, SiO2 was wrapped on Fe3O4 nanospheres assembled in a chain to form a Fe3O4@SiO2 nanocomposite with a chain-like nanostructure. Then, the magnetic Fe3O4@SiO2@Au/PDA nanochains were prepared using in situ redox-oxidization polymerization. Under the irradiation of an 808 nm NIR laser, the temperature rise of the Fe3O4@SiO2@Au/PDA nanochain dispersion was obvious, indicating that they possessed a good photothermal effect. Originating from the Fe3O4, the Fe3O4@SiO2@Au/PDA nanochain showed a typical soft magnetic behavior. Both the NIR and magnetic field affected the antimicrobial performance of the Fe3O4@SiO2@Au/PDA nanochains. Escherichia coli and Staphylococcus aureus were used as models to verify the antibacterial properties. The experimental results showed that the Fe3O4@SiO2@Au/PDA nanochains exhibited good antibacterial properties under photothermal conditions. After applying a magnetic field, the bactericidal effect was further significantly enhanced. The above results show that the material has a broad application prospect in inhibiting the growth of bacteria.


Introduction
There are a large number of pathogenic bacteria in the environment of daily life, which seriously threaten people's physical and mental health. In order to meet the increasingly sophisticated needs of the public for health and safety, scientists have been trying to develop a variety of efficient and safe antibacterial drugs. So far, the use of antibiotics is still the most widespread method to treat diseases caused by bacterial infections [1][2][3]. As bacterial infections become more and more serious, antibiotics are used in large quantities, which leads to a great increase in the resistance of bacteria, thereby reducing the therapeutic effect of antibiotics. Especially in the case of local treatment, such as skin lesion or breast cancers, safer treatment is urgently required for the application to have precise targeting, avoiding greater risks to the patient. Therefore, researchers are actively looking for effective methods to treat bacterial infections without causing high drug resistance.
The photothermal therapy of bacteria under near-infrared light irradiation has attracted wide attention due to its unique treating effects [4][5][6]. Photothermal therapy (PTT), as a new technology for the treatment of bacterial infections, has many advantages such as low damage to the body, good antibacterial effects, and low toxicity and side effects. Since photothermal therapy physically kills bacteria through thermal ablation, it can effectively reduce the generation of bacterial drug resistance, thus showing broad application prospects [7][8][9][10]. Considering that PTT also shows some drawbacks such as non-specificity and low penetration, intensive research has been conducted to improve PTT's performance and clarify its mechanism. With the development of nanotechnology, the combination of photothermal therapy with nanomaterials has introduced novel possibilities for antibacterial treatment. During the past decade, various nanomaterials with unique photothermal activity, such as noble metals, semiconductor nanocrystals, and carbon materials, have been intensively studied [11][12][13][14][15]. In addition to their high photothermal effects, multifunctional PTT nanoplatforms with fewer side effects are of special vital importance in developing novel therapeutics against bacterial infections. As a result, core/shell-structured PTT nanocomposites have become attractive since their high surface-modification activity, high biocompatibility, high light-to-heat conversion efficiency, and low toxicity can effectively improve antibacterial performance [16,17].
Magnetic nanocomposites could introduce photothermal nanoplatforms with advantages such as high photothermal conversion, strong magnetic properties, and easy separation [18]. Fe 3 O 4 nanoparticles have been explored in different bacterial and drug-delivery nanosystems due to their wonderful magnetic characteristics. Based on magnetic Fe 3 O 4 nanocrystals, many photothermal nanoplatforms have been studied. Li et al. designed a polydopamine-modified Fe 3 O 4 nanocomposite as a magnetic therapeutic nanoagent for MRI-guided photothermal therapy (PTT) to treat cancer [19]. Zhang et al. successfully prepared Fe 3 O 4 @CuS photothermal microspheres using a simple chemical deposition method [20]. Getiren et al. synthesized a core-shell structured superparamagnetic Fe 3 O 4 @PPy nanocomposite with a strong near-infrared absorption [21]. These materials all have a spherical structure and exhibit excellent performance in antibacterial applications. Recently, it was found that magnetic NiFe 2 O 4 @Au/PDA nanospheres exhibit a high antibacterial performance [22]. Under an applied magnetic field, the photothermal antibacterial effect increased due to the magnetically induced forces on the magnetic nanospheres. Moreover, this wonderful magnetolytic effect has also been shown in the MXene@Fe 3 O 4 /Au/PDA nanosheet photothermal antibacterial system [23]. Obviously, the nanostructure of the magnetic nanocomposites also plays an important role in magnetophotothermal antibacterial performance. As a result, more work should be conducted to develop special magnetic nanostructures and investigate the magnetic-field-induced improvement of photothermal sterilization performance.
Polydopamine (PDA) is a wonderful biocompatible polymer which has the advantages of simple preparation, high adhesion, and easy functionalization. Due to its low cytotoxicity and good binding ability to target cells, PDA has been widely applied to cover nanomaterials to form various functional nanomedicines [22,23]. In this work, a NIR-lightactivated antibacterial system based on Fe 3 O 4 @SiO 2 @Au/PDA nanochains is developed to realize the coupling of high magnetolytic and photothermal antibacterial activity and low cytotoxicity. Due to the presence of a polydopamine (PDA) shell, sandwiched Au nanocrystals, and an inner magnetic Fe 3 O 4 core, the biocompatible Fe 3 O 4 @SiO 2 @Au/PDA nanochains have both photothermal effects and magnetic-field-guided effects. When the concentration of Fe 3 O 4 @SiO 2 @Au/PDA nanochains is 500 µg/mL, the temperature rises to 57 • C if irradiated by an 808 nm laser for 5 min, and the photothermal conversion efficiency is 44.26%. Moreover, the coupled photothermal therapy and magnetic-guided antibacterial properties against Escherichia coli and Staphylococcus aureus were clearly observed under the simultaneous introduction of NIR and a magnetic field. This material shows excellent magnetolytic-photothermal coupling inhibitory effects, and thus possesses a high potential for future antibacterial strategy development.  NO 3 Si), and 3-hydroxytyrosine hydrochloride (DA-HCl) were bought from Aladdin Reagent (Shanghai, China). All chemicals were used as received without any further purification. The water used in the experiment was ultrapure water.

Preparation of Fe 3 O 4 @SiO 2 Nanochain
First, Fe 3 O 4 nanoparticles were synthesized through a one-pot solvothermal reaction [24]. Generally, FeCl 3 ·6H 2 O (1.08 g) was dissolved in a mixed solution of ethylene glycol (10 mL) and diethylene glycol (30 mL). After being completely dissolved, polyacrylamide (PAA) was added under continuous stirring. After thorough mixing, the homogeneous mixture was transferred and sealed in a stainless steel autoclave lined with polytetrafluoroethylene (PTFE) and heated to 200 • C. Twelve hours later, the system was cooled to room temperature and the obtained Fe 3 O 4 nanoparticles were washed alternately with deionized water and ethanol 4 times. Then, the product was dried using a static magnetic field under vacuum at 40 • C for 12 h.
Next, the Fe 3 O 4 @SiO 2 was prepared. First, 10 mg Fe 3 O 4 was dispersed in ethanol (30 mL) and deionized water (3 mL). After it was uniformly dispersed, 1.8 mL of ammonia monohydrate was added. After sonicating for 10 min, 0.2 mL of TEOS was added. The reaction was conducted for 1.5 h. After the reaction, the product was collected from the solution with a magnet. The obtained black solid was washed with deionized ethanol several times, and dried under vacuum for 12 h to obtain a dark gray powder.

Preparation of Core/Shell Structure Fe 3 O 4 @SiO 2 @Au/PDA Nanochain
The aforementioned Fe 3 O 4 @SiO 2 was used as the core template to synthesize the Fe 3 O 4 @SiO 2 @Au/PDA core/shell nanochains. First, 15 mg Fe 3 O 4 @SiO 2 was ultrasonically dispersed in 50 mL of C 2 H 5 OH. Next, 15 mg of sodium citrate and 60 µL of HAuCl 4 were added to form a mixed solution. Then, 45 mg dopamine was added to 45 mL of Tris (pH = 8.5) to form another solution. After complete dissolution, the two solutions were mixed. After 3 h sonication, the product was collected from the solution using magnetic separation. The obtained black solid was washed alternately with deionized water and ethanol, and dried under vacuum for 12 h to obtain a black powder.

The Photothermal Effect of Fe 3 O 4 @SiO 2 @Au/PDA Nanochain
The prepared Fe 3 O 4 @SiO 2 @Au/PDA standard solution was diluted into 100 µg/mL, 200 µg/mL, 300 µg/mL, 400 µg/mL, and 500 µg/mL solutions. A 2 mL volume of Fe 3 O 4 @SiO 2 @Au/PDA solution at a concentration of 100 µg/mL was placed in a 4 mL centrifuge tube. Under the irradiation of an 808 nm near-infrared laser, the temperature of the solution was recorded with an infrared camera every 20 s. The influence of the different concentrations of Fe 3 O 4 @SiO 2 @Au/PDA solutions on the temperature was also recorded using this method.
2.5. Photothermal Therapy (PTT) and Magnetic Guidance Effect Synergistic Sterilization of the Fe 3 O 4 @SiO 2 @Au/PDA Nanochain First, a certain amount of LB agar medium and broth medium were prepared in proportion. After high-temperature sterilization and cooling, the LB agar medium was shaken in the ultra-clean platform and then was poured into Petri dishes. The Petri dishes were placed horizontally. Then, a certain amount of the original bacterial solution was added to the sterilized broth medium for 10 h to obtain the bacteria in the logarithmic growth phase. Samples with different concentrations were prepared with sterilized LB agar medium, and the experimental group and blank control were set. Escherichia coli or Staphylococcus aureus were added to the experimental groups and treated under different conditions (Group 1: Petri dishes were irradiated with a laser only; Group 2: after laser irradiation, magnetic field treatment was performed). Bacterial suspensions were treated with an NIR laser (L, 2.5 W cm −2 ) and/or a rotating magnetic field (RMF, 15 mT, 350 rpm), and the three groups were labeled as Control, PTT, and PTT + Magnet, respectively. Except for the control group, the treatment time was 6 min, where PTT + Magnet was the combined action of NIR laser and rotating magnetic field for 6 min. During the magnetic treatment, the magnetic field was applied using a magnetic stirrer directly under the solution. In the control group, only bacteria and materials were added without any treatment. The above solution was placed in a 37 • C constant-temperature incubator for 24 h. The co-culture bacterial liquid was gradually diluted with a 24-well plate as a container, and a certain amount of the diluted bacterial liquid was absorbed and coated on the prepared Petri dish, and then placed in an incubator at 37 • C for cultivation for 24 h to observe the growth of the bacterial colony.
2.6. MTT Cell Assays of the Fe 3 O 4 @SiO 2 @Au/PDA Nanochains The biocompatibility and cytotoxicity of Fe 3 O 4 @SiO 2 @Au/PDA nanochains were evaluated with MTT cell assays in human umbilical vein endothelial cells (HUVEC). Under standard conditions (37 • C, 5% CO 2 ), 10% fetal bovine serum (FBS) was added to DMEM medium (Dulbecco's Modified Eagle Medium, a medium containing various amino acids and glucose). HUVEC in the logarithmic growth phase were inoculated on 96-well cell culture plates (1 × 10 4 cells per well, 200 µL) and incubated for 24 h. Then, fresh DMEM medium containing Fe 3 O 4 @SiO 2 @Au/PDA nanochains (with different gradient concentrations) was replaced and incubated for another 24 h. HUVEC were washed with fresh medium and cell viability was confirmed using a standard MTT assay according to the manufacturer's protocol.

Characterization
The morphologies of the nanocomposites were studied using a JEM-2100 F field emission transmission electron microscope (FE-TEM, JEOL, Tokyo, Japan) operating at 200 kV acceleration voltage. The EDS spectra were investigated with the JEM-2100 F field emission transmission electron microscope (FE-TEM). Field emission scanning electron microscopy (FE-SEM) images were operated on a Regulus 8230 HR-FESEM (Hitachi, Tokyo, Japan). The XRD patterns were obtained with a Bruker D8 Advance diffractometer (Karlsruhe, Germany), which was equipped with graphite monochromatized Cu Kα radiation (λ =1.5406 Å). The X-ray photoelectron spectra (XPS) were recorded with an ESCALAB 250(Thermo Scientific, Walthamm, MA, USA). Thermogravimetric (TG) analysis was performed on a DTG-60H thermogravimetric instrument and the nanocomposites were analyzed under air flowing from room temperature to 800 • C at a heating rate of 10 • C min −1 . Hysteresis loops were measured on a vibrating sample magnetometer (SQUID-VSM, QuantumDesign, San Diego, CA, USA) at 300 K.

Results and Discussion
Scheme 1 shows the synthetic illustration of the Fe 3 O 4 @SiO 2 @Au/PDA nanochains. First, the Fe 3 O 4 nanospheres were assembled to form chain-like nanostructures during synthesis. Then, the SiO 2 was coated on the Fe 3 O 4 nanochains to form the Fe 3 O 4 @SiO 2 core/shell nanochains. At last, the Au/PDA hybrid shell further covered the above particles via an in situ redox-oxidization polymerization method through the reaction between HAuCl 4 and dopamine [25]. Figure 1a shows the SEM of the obtained Fe 3 O 4 @SiO 2 @Au/PDA nanochains. It can be seen that the synthesized chain-like nanostructures have different lengths and their shapes are similar to candied haws. Figure 1b shows the TEM image of the product, which agrees well with the SEM analysis. The samples in the entire field of view are all chain-like structures (Figure 1c), indicating the successful synthesis of chain-like Fe 3 O 4 @SiO 2 @Au/PDA nanostrings. Figure 1d is the high-power transmission electron micrograph. It can be observed that the obtained Fe 3 O 4 @SiO 2 @Au/PDA nanochain has an obvious core/shell nanostructure. The outermost shell layer is a transparent PDA layer and it is uniformly coated on the surface of the nanochain. The sandwiched black layer is a discontinuous layer of Au nanoparticles and the inner black spherical core/shell structure is Fe 3 O 4 @SiO 2 nanochain. samples in the entire field of view are all chain-like structures (Figure 1c), indicating the successful synthesis of chain-like Fe3O4@SiO2@Au/PDA nanostrings. Figure 1d is the highpower transmission electron micrograph. It can be observed that the obtained Fe3O4@SiO2@Au/PDA nanochain has an obvious core/shell nanostructure. The outermost shell layer is a transparent PDA layer and it is uniformly coated on the surface of the nanochain. The sandwiched black layer is a discontinuous layer of Au nanoparticles and the inner black spherical core/shell structure is Fe3O4@SiO2 nanochain.  To further understand the inner nanostructure and composition of the final product, high-angle annular dark-field scanning electron microscopy (HAADF-STEM) and energy dispersive X-ray spectroscopy (EDX) elemental maps were created. As shown in Figure 2, the HAADF-STEM also confirms that the Fe3O4@SiO2@Au/PDA nanocomposite is a qua-Scheme 1. Schematic diagram of photothermal-magnetic coupled sterilization of Fe 3 O 4 @SiO 2 @Au/ PDA nanochains. samples in the entire field of view are all chain-like structures (Figure 1c), indicating the successful synthesis of chain-like Fe3O4@SiO2@Au/PDA nanostrings. Figure 1d is the highpower transmission electron micrograph. It can be observed that the obtained Fe3O4@SiO2@Au/PDA nanochain has an obvious core/shell nanostructure. The outermost shell layer is a transparent PDA layer and it is uniformly coated on the surface of the nanochain. The sandwiched black layer is a discontinuous layer of Au nanoparticles and the inner black spherical core/shell structure is Fe3O4@SiO2 nanochain.  To further understand the inner nanostructure and composition of the final product, high-angle annular dark-field scanning electron microscopy (HAADF-STEM) and energy dispersive X-ray spectroscopy (EDX) elemental maps were created. As shown in Figure 2, the HAADF-STEM also confirms that the Fe3O4@SiO2@Au/PDA nanocomposite is a qua- To further understand the inner nanostructure and composition of the final product, high-angle annular dark-field scanning electron microscopy (HAADF-STEM) and energy dispersive X-ray spectroscopy (EDX) elemental maps were created. As shown in Figure 2, the HAADF-STEM also confirms that the Fe 3 O 4 @SiO 2 @Au/PDA nanocomposite is a quaternary component core/shell nanochain (Figure 2a,b). By observing the element distribution map of Fe, it can be seen that the image size of the Fe element is small (about 70 nm) and it is mainly located in the core (Figure 2a,c). Clearly, the Fe elements collected with each other to form a chain-like nanostructure, which also demonstrates that the Fe 3 O 4 nanochains are formed by the Fe 3 O 4 nanospheres. Figure 2d illustrates that the size of Si is obviously larger than that of Fe, which indicates that SiO 2 covers the surface of Fe 3 O 4 . After the SiO 2 coating, the diameter of the nanochain increases to about 120 nm. The O element shows a similar distribution size with the Si, demonstrating that this immediate shell is composed of SiO 2 ( Figure 2e). Here, the Au/PDA layer is simultaneously coated on the surface of the Fe 3 O 4 @SiO 2 , thus the distribution size of Au is beyond the Si (Figure 2f). However, the distribution density of Au in the core is low and the Au nanocrystals are immobilized around the SiO 2 with a non-continuous nature. This result matches the above TEM analysis. The diameters of the elemental profiles of C and N are approximately the same (Figure 2g,h), further proving that the PDA shell uniformly coats the surface of Fe 3 O 4 @SiO 2 . The size of the N is a little larger than the Au, demonstrating the Au nanocrystals are encapsulated by the PDA shell. Based on the above analysis, it can be concluded that the Fe 3 O 4 @SiO 2 @Au/PDA nanochain with core/shell structure was successfully synthesized. each other to form a chain-like nanostructure, which also demonstrates that the Fe3O4 nanochains are formed by the Fe3O4 nanospheres. Figure 2d illustrates that the size of Si is obviously larger than that of Fe, which indicates that SiO2 covers the surface of Fe3O4. After the SiO2 coating, the diameter of the nanochain increases to about 120 nm. The O element shows a similar distribution size with the Si, demonstrating that this immediate shell is composed of SiO2 ( Figure 2e). Here, the Au/PDA layer is simultaneously coated on the surface of the Fe3O4@SiO2, thus the distribution size of Au is beyond the Si (Figure 2f). However, the distribution density of Au in the core is low and the Au nanocrystals are immobilized around the SiO2 with a non-continuous nature. This result matches the above TEM analysis. The diameters of the elemental profiles of C and N are approximately the same (Figure 2g,h), further proving that the PDA shell uniformly coats the surface of Fe3O4@SiO2. The size of the N is a little larger than the Au, demonstrating the Au nanocrystals are encapsulated by the PDA shell. Based on the above analysis, it can be concluded that the Fe3O4@SiO2@Au/PDA nanochain with core/shell structure was successfully synthesized. The TEM was also applied to analyze the synthesis of the Fe3O4@SiO2@Au/PDA nanochains. Here, the Fe3O4 nanochains assembled by Fe3O4 nanospheres were firstly obtained using the solvothermal method (Figure 3a). During the preparation, they were dried under a static magnetic field in vacuum at 40 °C for 12 h; thus, the Fe3O4 nanospheres assembled to form a chain-like nanostructure since they tend to align with the magnetic flux lines. Due to the interaction of PAA residues in the Fe3O4 nanospheres, the chain-like nanostructure assembled from the Fe3O4 nanospheres is relatively stable (Figure 3b). Therefore, they can be applied as the chain template for the following coating process. In the preparation of Fe3O4@SiO2 nanochains, the chain-like Fe3O4 (a single Fe3O4 with 70 nm) was added to the ethanol solution and ultrasonically dispersed. After introducing ammonia and tetra-orthosilicate, the reaction was started and the Fe3O4@SiO2 nanochains were obtained (Figure 3c). The introduction of the SiO2 coating was to make the chain structure more stable. Obviously, the size of the nanochain increases and the Fe3O4@SiO2 nanochains show the typical core/shell nanostructure. Then, using the Fe3O4@SiO2 nanochain as the template, the Fe3O4@SiO2@Au/PDA could be successfully obtained with the reaction between HAuCl4 and dopamine. HAuCl4 quickly reacted with the dopamine monomer to form Au nanoparticles and PDA polymer chains. The in situ-formed Au nanocrystals The TEM was also applied to analyze the synthesis of the Fe 3 O 4 @SiO 2 @Au/PDA nanochains. Here, the Fe 3 O 4 nanochains assembled by Fe 3 O 4 nanospheres were firstly obtained using the solvothermal method (Figure 3a). During the preparation, they were dried under a static magnetic field in vacuum at 40 • C for 12 h; thus, the Fe 3 O 4 nanospheres assembled to form a chain-like nanostructure since they tend to align with the magnetic flux lines. Due to the interaction of PAA residues in the Fe 3 O 4 nanospheres, the chainlike nanostructure assembled from the Fe 3 O 4 nanospheres is relatively stable (Figure 3b). Therefore, they can be applied as the chain template for the following coating process. In the preparation of Fe 3 O 4 @SiO 2 nanochains, the chain-like Fe 3 O 4 (a single Fe 3 O 4 with 70 nm) was added to the ethanol solution and ultrasonically dispersed. After introducing ammonia and tetra-orthosilicate, the reaction was started and the Fe 3 O 4 @SiO 2 nanochains were obtained (Figure 3c). The introduction of the SiO 2 coating was to make the chain structure more stable. Obviously, the size of the nanochain increases and the Fe 3 O 4 @SiO 2 nanochains show the typical core/shell nanostructure. Then, using the Fe 3 O 4 @SiO 2 nanochain as the template, the Fe 3 O 4 @SiO 2 @Au/PDA could be successfully obtained with the reaction between HAuCl 4 and dopamine. HAuCl 4 quickly reacted with the dopamine monomer to form Au nanoparticles and PDA polymer chains. The in situ-formed Au nanocrystals were protected by the polydopamine (PDA) polymer and they tended to attach onto the surface of the Fe 3 O 4 @SiO 2 nanochains to form Fe 3 O 4 @SiO 2 @Au/PDA nanochains (Figure 3d). Due to the low concentration of HAuCl 4 in our synthesis, the Au nanocrystals showed a non-continuous layer on the Fe 3 O 4 @SiO 2 and they were encapsulated by the external PDA shell.
The chainlike Fe 3 O 4 nanostructure plays a critical role in forming the Fe 3 O 4 @SiO 2 @Au/ PDA nanochains. As a comparison, a Fe 3 O 4 @SiO 2 @Au/PDA nanosphere would be obtained using the monodispersed Fe 3 O 4 nanosphere as the starting material. Figure 4a indicates that the monodispersed Fe 3 O 4 nanosphere has a diameter of about 70 nm. After the SiO 2 coating using the sol-gel method, the diameter of the Fe 3 O 4 @SiO 2 core/shell nanosphere increased to 130 nm, and the thickness of the SiO 2 shell layer was about  (Figure 4b). After the further Au/PDA coating, the product showed an obvious four-layer structure, in which the outermost was the discontinuous Au layer and the continuous and uniform PDA layer (Figure 4c). Figure 4d shows a typical TEM image of a single Fe 3 O 4 @SiO 2 @Au/PDA nanosphere. It is observed that the diameter of Au is about 10 nm and the thickness of the PDA shell is about 20 nm, thus the average size of Fe 3 O 4 @SiO 2 @Au/PDA nanoparticles is about 200 nm. were protected by the polydopamine (PDA) polymer and they tended to attach onto the surface of the Fe3O4@SiO2 nanochains to form Fe3O4@SiO2@Au/PDA nanochains ( Figure  3d). Due to the low concentration of HAuCl4 in our synthesis, the Au nanocrystals showed a non-continuous layer on the Fe3O4@SiO2 and they were encapsulated by the external PDA shell. The chainlike Fe3O4 nanostructure plays a critical role in forming the Fe3O4@SiO2@Au/PDA nanochains. As a comparison, a Fe3O4@SiO2@Au/PDA nanosphere would be obtained using the monodispersed Fe3O4 nanosphere as the starting material. Figure 4a indicates that the monodispersed Fe3O4 nanosphere has a diameter of about 70 nm. After the SiO2 coating using the sol-gel method, the diameter of the Fe3O4@SiO2 core/shell nanosphere increased to 130 nm, and the thickness of the SiO2 shell layer was about 30 nm (Figure 4b). After the further Au/PDA coating, the product showed an obvious four-layer structure, in which the outermost was the discontinuous Au layer and the continuous and uniform PDA layer (Figure 4c). Figure 4d shows a typical TEM image of a single Fe3O4@SiO2@Au/PDA nanosphere. It is observed that the diameter of Au is about 10 nm and the thickness of the PDA shell is about 20 nm, thus the average size of Fe3O4@SiO2@Au/PDA nanoparticles is about 200 nm.  In order to fully investigate the nanostructure of Fe3O4@SiO2@Au/PDA nanospheres, high-angle circular dark-field scanning TEM (HAADF-STEM) images were studied. As shown in Figure 5, TEM images of high-angle dark-field annular scanning indicated that Fe3O4@SiO2 core/shell nanostructure is present inside the Fe3O4@SiO2@Au/PDA nanocomposite. The Si element shows a weak hollow morphology, indicating the SiO2 covers the In order to fully investigate the nanostructure of Fe 3 O 4 @SiO 2 @Au/PDA nanospheres, high-angle circular dark-field scanning TEM (HAADF-STEM) images were studied. As shown in Figure 5, TEM images of high-angle dark-field annular scanning indicated that Fe 3 O 4 @SiO 2 core/shell nanostructure is present inside the Fe 3 O 4 @SiO 2 @Au/PDA nanocomposite. The Si element shows a weak hollow morphology, indicating the SiO 2 covers the Fe 3 O 4 nanosphere to form the core/shell nanostructure. In comparison to the Si and O elements, the distribution size of the Au is larger, which further proves the Au nanocrystals are immobilized on the surface of the SiO 2 shell. The N element is detected in Fe 3 O 4 @SiO 2 @Au/PDA nanospheres, demonstrating that the whole nanosphere is encapsulated within a PDA shell. It can be found that below the Au/PDA hybrid layer is the SiO 2 shell with a thickness of about 60 nm and the central core part is Fe 3 O 4 superparamagnetic nanosphere. Based on the above analysis, it is concluded that the Fe 3 O 4 @SiO 2 @Au/PDA core/shell nanostructure was successfully prepared using the Fe 3 O 4 nanosphere as the template. If the core changes to the Fe 3 O 4 nanochain, the Fe 3 O 4 @SiO 2 @Au/PDA nanochain will be obtained. The synthesis process of the sample can be tracked using thermogravimetry. As shown in Figure 6a. The weight loss rates of Fe3O4, Fe3O4@SiO2, and Fe3O4@SiO2@Au/PDA nanochains are 9.38 wt%, 9.8 wt%, and 17.1 wt%, respectively. With increasing temperature, the weight of Fe3O4 begins to decrease, which must originated from the decomposition of the organic groups and water contained in the Fe3O4 nanochains. When the surface of the Fe3O4 nanochain is coated with an SiO2 shell, its weight loss is about 4.2 wt% higher than that of Fe3O4 due to the high water absorbance in the SiO2 shell prepared with the sol-gel process. After further coating the Au/PDA layer on the Fe3O4@SiO2, the weight loss of Fe3O4@SiO2@Au/PDA nanocomposite is further increased. This result is owing to the PDA's decomposition at high temperatures which causes a larger mass loss.
To further study the internal structure of the Fe3O4@SiO2@Au/PDA nanocomposite, XPS (X-ray photoelectron spectroscopy) was used to analyze the element composition on the surface of the samples. Figure 6b shows the XPS spectra of Fe3O4, Fe3O4@SiO2, and Fe3O4@SiO2@Au/PDA nanochains. The strong signal peaks of Fe, C, and O elements can be clearly observed in the XPS spectrum of Fe3O4. After coating with SiO2, an obvious signal peak of Si is detected in the Fe3O4@SiO2, which indicates the existence of the SiO2 shell. At the same time, it can be seen that the Fe signal peak disappears, which indicates that the SiO2 shell has successfully coated the Fe3O4 surface and blocked the Fe signal. When the Au/PDA layer covers the surface of the Fe3O4@SiO2 to form the Fe3O4@SiO2@Au/PDA nanochains, the typical Au signal peaks and N signal peaks can be observed. Here, the N element comes from the PDA layer. Based on the above analysis, it can be concluded that Fe3O4@SiO2@Au/PDA nanochains were successfully prepared using the simple method. The synthesis process of the sample can be tracked using thermogravimetry. As shown in Figure 6a. The weight loss rates of Fe 3 O 4 , Fe 3 O 4 @SiO 2 , and Fe 3 O 4 @SiO 2 @Au/PDA nanochains are 9.38 wt%, 9.8 wt%, and 17.1 wt%, respectively. With increasing temperature, the weight of Fe 3 O 4 begins to decrease, which must originated from the decomposition of the organic groups and water contained in the Fe 3 O 4 nanochains. When the surface of the Fe 3 O 4 nanochain is coated with an SiO 2 shell, its weight loss is about 4.2 wt% higher than that of Fe 3 O 4 due to the high water absorbance in the SiO 2 shell prepared with the sol-gel process. After further coating the Au/PDA layer on the Fe 3 O 4 @SiO 2 , the weight loss of Fe 3 O 4 @SiO 2 @Au/PDA nanocomposite is further increased. This result is owing to the PDA's decomposition at high temperatures which causes a larger mass loss.
To further study the internal structure of the Fe 3 O 4 @SiO 2 @Au/PDA nanocomposite, XPS (X-ray photoelectron spectroscopy) was used to analyze the element composition on the surface of the samples. Figure 6b shows the XPS spectra of Fe 3 O 4 , Fe 3 O 4 @SiO 2 , and Fe 3 O 4 @SiO 2 @Au/PDA nanochains. The strong signal peaks of Fe, C, and O elements can be clearly observed in the XPS spectrum of Fe 3 O 4 . After coating with SiO 2 , an obvious signal peak of Si is detected in the Fe 3 O 4 @SiO 2 , which indicates the existence of the SiO 2 shell. At the same time, it can be seen that the Fe signal peak disappears, which indicates that the SiO 2 shell has successfully coated the Fe 3 O 4 surface and blocked the Fe signal. When the Au/PDA layer covers the surface of the Fe 3 O 4 @SiO 2 to form the Fe 3 O 4 @SiO 2 @Au/PDA nanochains, the typical Au signal peaks and N signal peaks can be observed. Here, the N element comes from the PDA layer. Based on the above analysis, it can be concluded that Fe 3 O 4 @SiO 2 @Au/PDA nanochains were successfully prepared using the simple method.  Figure 6c shows the XRD patterns of the Fe3O4, Fe3O4@SiO2, and Fe3O4@SiO2@Au/PDA nanochains. The characteristic peaks of all diffraction planes for Fe3O4 nanochains can be indexed as (220), (311), (440), (511), and (440) lattice planes with a face-centered cubic crystallization. Because the SiO2 is amorphous, no new diffraction peak is found in Fe3O4@SiO2. The XRD pattern of Fe3O4@SiO2 is similar to that of Fe3O4, which indicates that the SiO2 coating process does not affect the crystal phase of Fe3O4. When Au/PDA is further fixed on the Fe3O4@SiO2 surface, obvious Au diffraction peaks (111), (200), and (220) appeared at 38°, 44.1°, and 64.8°, respectively. This result also indicates the successful preparation of the Fe3O4@SiO2@Au/PDA nanochains. The magnetic properties of Fe3O4, Fe3O4@SiO2, and Fe3O4@SiO2/Au/PDA nanochains are shown in Figure  3d. Obviously, the magnetic properties of all samples originate from the Fe3O4 core. The saturation magnetization (Ms) of nanocomposites decreases with the addition of nonmagnetic SiO2 and Au/PDA hybrid layers. Although the Ms value of Fe3O4@SiO2@Au/PDA (19.5 emu/g) is lower than those of Fe3O4@SiO2 (30.1 emu/g) and Fe3O4 (70.1 emu/g), its magnetic response capacity is sufficient to use a magnet to remove it from the reaction system. More importantly, the Fe3O4@SiO2@Au/PDA nanochains possess a soft magnetic characteristic (the coercivity of the nanoparticles was smaller than 50 Oe, as shown in the inset of Figure 6d), which must exhibit high potential application prospects in nanocatalysis and targeted drugs.
Due to the presence of Au and PDA, the Fe3O4@SiO2@Au/PDA nanochains show light absorption and photothermal conversion properties. As shown in Figure 7a, the Fe3O4@SiO2@Au/PDA nanochains have strong and wide absorbance in the ultraviolet to near-infrared range, which gives them great potential in the near infrared light (NIR)triggered photothermal sterilization. With an increase in the laser irradiation time or Fe3O4@SiO2@Au/PDA concentration, the temperature of the nanochain suspension increases rapidly. After exposure for 300 s, the final temperature of the   Figure 3d. Obviously, the magnetic properties of all samples originate from the Fe 3 O 4 core. The saturation magnetization (Ms) of nanocomposites decreases with the addition of non-magnetic SiO 2 and Au/PDA hybrid layers. Although the Ms value of Fe 3 O 4 @SiO 2 @Au/PDA (19.5 emu/g) is lower than those of Fe 3 O 4 @SiO 2 (30.1 emu/g) and Fe 3 O 4 (70.1 emu/g), its magnetic response capacity is sufficient to use a magnet to remove it from the reaction system. More importantly, the Fe 3 O 4 @SiO 2 @Au/PDA nanochains possess a soft magnetic characteristic (the coercivity of the nanoparticles was smaller than 50 Oe, as shown in the inset of Figure 6d), which must exhibit high potential application prospects in nanocatalysis and targeted drugs.
Due to the presence of Au and PDA, the Fe 3 O 4 @SiO 2 @Au/PDA nanochains show light absorption and photothermal conversion properties. As shown in Figure 7a, the Fe 3 O 4 @SiO 2 @Au/PDA nanochains have strong and wide absorbance in the ultraviolet to near-infrared range, which gives them great potential in the near infrared light (NIR)triggered photothermal sterilization. With an increase in the laser irradiation time or Fe 3 O 4 @SiO 2 @Au/PDA concentration, the temperature of the nanochain suspension increases rapidly. After exposure for 300 s, the final temperature of the Fe 3 O 4 @SiO 2 @Au/PDA nanochain suspension with a concentration of 500 µg/mL was 57 • C. According to the temperature-rise curves of different samples in Figure 7b, the temperature increment of pure water is almost negligible under the same illumination time, while the temperature increment of Fe 3 O 4 @SiO 2 @Au/PDA nanochains is larger than the Fe 3 O 4 and Fe 3 O 4 @SiO 2 nanochains. Fe3O4@SiO2@Au/PDA nanochain suspension with a concentration of 500 μg/mL was 57 °C. According to the temperature-rise curves of different samples in Figure 7b, the temperature increment of pure water is almost negligible under the same illumination time, while the temperature increment of Fe3O4@SiO2@Au/PDA nanochains is larger than the Fe3O4 and Fe3O4@SiO2 nanochains. In addition, Fe3O4@SiO2@Au/PDA nanochains have excellent chemical stability and stable photothermal conversion properties. As shown in Figure 7c, the 500 μg/mL Fe3O4@SiO2@Au/PDA can still reach a similar temperature level after five bouts of NIR laser irradiation, which indicates that the Fe3O4@SiO2/Au/PDA nanochain has good photothermal stability and reusability. The photothermal conversion efficiency (η) is an important parameter to evaluate photothermal agents. According to the method established by Rope et al., [26] the accurate η value of the Fe3O4@SiO2@Au/PDA under 808 nm laser irradiation is calculated to be about 44.26% (Figure 7e,f), which is higher than previously reported inorganic photothermal nanomaterials, including Au nanorods (21%), Cu2-XSe NCs (22%), and Cu9S5 NCs (25.7%) [12]. Figure 7g shows near-infrared thermal images of a centrifuge tube containing Fe3O4@SiO2@Au/PDA (500 μg/mL) in aqueous solution. As In addition, Fe 3 O 4 @SiO 2 @Au/PDA nanochains have excellent chemical stability and stable photothermal conversion properties. As shown in Figure 7c, the 500 µg/mL Fe 3 O 4 @SiO 2 @Au/PDA can still reach a similar temperature level after five bouts of NIR laser irradiation, which indicates that the Fe 3 O 4 @SiO 2 /Au/PDA nanochain has good photothermal stability and reusability. The photothermal conversion efficiency (η) is an important parameter to evaluate photothermal agents. According to the method established by Rope et al., [26] the accurate η value of the Fe 3 O 4 @SiO 2 @Au/PDA under 808 nm laser irradiation is calculated to be about 44.26% (Figure 7e,f), which is higher than previously reported inorganic photothermal nanomaterials, including Au nanorods (21%), Cu 2 -X Se NCs (22%), and Cu 9 S 5 NCs (25.7%) [12]. Figure 7g shows near-infrared thermal images of a centrifuge tube containing Fe 3 O 4 @SiO 2 @Au/PDA (500 µg/mL) in aqueous solution. As can be seen from the figure, after 7 min laser irradiation, the inside of the centrifuge tube turns red and the temperature rises significantly. These results directly indicate that Fe 3 O 4 @SiO 2 @Au/PDA nanochains exhibit excellent photothermal activity.
Biocompatibility is very important for nanomedicine, since a toxic nanomaterial cannot be applied. Human umbilical vein endothelial cells (HUVEC) are commonly applied to test the cell viability of nanomedicines. In this work, the biocompatibility of the Fe 3 O 4 @SiO 2 @Au/PDA nanochains was tested with an in vitro MTT activity study and apoptosis determination. In vitro biocompatibility and cytotoxicity of Fe 3 O 4 @SiO 2 @Au/PDA nanochains were evaluated using MTT cell assays in human umbilical vein endothelial cells (HUVEC). Under standard conditions (37°C, 5% CO 2 ), 10% fetal bovine serum (FBS) was added to DMEM and HUVEC in the logarithmic growth phase was inoculated on 96-well cell culture plates (1×10 4 cells per well, 200 µL) and incubated for 24 h. Then, fresh DMEM medium containing Fe 3 O 4 @SiO 2 @Au/PDA nanochains (with different gradient concentrations) was replaced and incubated for another 24 h. HUVEC was washed with fresh medium and cell viability was confirmed using a standard MTT assay according to the manufacturer's protocol. As shown in Figure 8, the Fe 3 O 4 @SiO 2 @Au/PDA nanochains are biocompatible and basically non-toxic. Therefore, this kind of material can be further applied in medicine. turns red and the temperature rises significantly. These results directly indicate that Fe3O4@SiO2@Au/PDA nanochains exhibit excellent photothermal activity. Biocompatibility is very important for nanomedicine, since a toxic nanomaterial cannot be applied. Human umbilical vein endothelial cells (HUVEC) are commonly applied to test the cell viability of nanomedicines. In this work, the biocompatibility of the Fe3O4@SiO2@Au/PDA nanochains was tested with an in vitro MTT activity study and apoptosis determination. In vitro biocompatibility and cytotoxicity of Fe3O4@SiO2@Au/PDA nanochains were evaluated using MTT cell assays in human umbilical vein endothelial cells (HUVEC). Under standard conditions (37℃, 5% CO2), 10% fetal bovine serum (FBS) was added to DMEM and HUVEC in the logarithmic growth phase was inoculated on 96-well cell culture plates (1×10 4 cells per well, 200 μL) and incubated for 24 h. Then, fresh DMEM medium containing Fe3O4@SiO2@Au/PDA nanochains (with different gradient concentrations) was replaced and incubated for another 24 h. HUVEC was washed with fresh medium and cell viability was confirmed using a standard MTT assay according to the manufacturer's protocol. As shown in Figure 8, the Fe3O4@SiO2@Au/PDA nanochains are biocompatible and basically non-toxic. Therefore, this kind of material can be further applied in medicine. Owing to its wonderful photothermal effect, Fe3O4@SiO2@Au/PDA nanochains can be applied as a PTT reagent. To evaluate the antibacterial properties of Fe3O4@SiO2@Au/PDA nanochains, the inhibition of bacterial growth under different conditions was studied using Escherichia coli as a bacterial model. First, three groups of samples with different concentration gradients (0, 200, 400 μg/mL) were prepared and added into LB medium. One group was set as blank control group, and the other two groups were experimental groups with PTT or PTT/Magnetic conditions. Here, PTT means the experiment is conducted by applying an 808 nm NIR laser for 10 min and PTT/Magnetic means both NIR and a magnetic field are applied.
Then, the experimental groups treated under different conditions were placed in an incubator at 37 °C for 12 h. Finally, a certain amount of culture solution was absorbed and coated on the prepared plate, and then placed in an incubator at 37 ℃ for cultivation for 24 h to observe the growth of the colony. Figure 9 shows the antibacterial performance of the Fe3O4@SiO2@Au/PDA nanochains against Escherichia coli. Clearly, the Escherichia coli in Owing to its wonderful photothermal effect, Fe 3 O 4 @SiO 2 @Au/PDA nanochains can be applied as a PTT reagent. To evaluate the antibacterial properties of Fe 3 O 4 @SiO 2 @Au/PDA nanochains, the inhibition of bacterial growth under different conditions was studied using Escherichia coli as a bacterial model. First, three groups of samples with different concentration gradients (0, 200, 400 µg/mL) were prepared and added into LB medium. One group was set as blank control group, and the other two groups were experimental groups with PTT or PTT/Magnetic conditions. Here, PTT means the experiment is conducted by applying an 808 nm NIR laser for 10 min and PTT/Magnetic means both NIR and a magnetic field are applied.
Then, the experimental groups treated under different conditions were placed in an incubator at 37 • C for 12 h. Finally, a certain amount of culture solution was absorbed and coated on the prepared plate, and then placed in an incubator at 37°C for cultivation for 24 h to observe the growth of the colony. Figure 9 shows the antibacterial performance of the Fe 3 O 4 @SiO 2 @Au/PDA nanochains against Escherichia coli. Clearly, the Escherichia coli in the control group without any external treatment show a good growth trend (the first row of Figure 9), and the increasing concentration of the Fe 3 O 4 @SiO 2 @Au/PDA nanochains shows few effects on the growth of the bacteria, which also agrees that the prepared materials are biocompatible. If no sample was added (the first column of Figure 9), the growth trend of Escherichia coli was almost the same, which ruled out the influence of NIR and magnetic field on bacterial growth. Under NIR laser irradiation alone, the Fe 3 O 4 @SiO 2 @Au/PDA nanochains showed a clear sterilization against Escherichia coli due to the thermal effect. Moreover, with an increase in the concentration, the sterilization effect was better. This result is because the larger the concentration of the Fe 3 O 4 @SiO 2 @Au/PDA nanochains, the stronger the absorption at 808 nm, and the higher the photothermal effect. As a result, the sterilization effect becomes better. the control group without any external treatment show a good growth trend (the first row of Figure 9), and the increasing concentration of the Fe3O4@SiO2@Au/PDA nanochains shows few effects on the growth of the bacteria, which also agrees that the prepared materials are biocompatible. If no sample was added (the first column of Figure 9), the growth trend of Escherichia coli was almost the same, which ruled out the influence of NIR and magnetic field on bacterial growth. Under NIR laser irradiation alone, the Fe3O4@SiO2@Au/PDA nanochains showed a clear sterilization against Escherichia coli due to the thermal effect. Moreover, with an increase in the concentration, the sterilization effect was better. This result is because the larger the concentration of the Fe3O4@SiO2@Au/PDA nanochains, the stronger the absorption at 808 nm, and the higher the photothermal effect. As a result, the sterilization effect becomes better. Under the NIR laser irradiation, if an external magnetic field is introduced, the sterilization effect of Fe3O4@SiO2@Au/PDA nanochains at the same concentration also shows an enhanced effect. During the treatment, Escherichia coli sinks to the bottom of the centrifuge tube due to the action of gravity. In the presence of an external magnetic field, the Fe3O4@SiO2@Au/PDA nanochains are subjected to the Lorentz force in the magnetic field and converge towards the magnetic field (Scheme 1). At this time, there will be a continuous penetrating force on the bacteria. This may be the reason why the sterilization effect is better than that of simple photothermal sterilization. As a result, the Fe3O4@SiO2@Au/PDA nanochains possess a wonderful coupled magnetolytic-photothermal inhibitory effect (Figure 9). It was found that the Fe3O4@SiO2@Au/PDA nanochains exhibited a unique photothermal effect and thus possess photothermal antibacterial behavior. The magnetic field induced the magnetic nanochains to form a magnetic force which further led to physical damage to the bacteria. As a result, the Fe3O4@SiO2@Au/PDA nanochains possess a coupled magnetic-photothermal antibacterial effect. Here, the magnetic properties of the Fe3O4@SiO2@Au/PDA nanochains do not improve the photothermal property but enhance the antibacterial performance.
Similar to the Escherichia coli, the Fe3O4@SiO2@Au/PDA nanochains also show a coupled magnetolytic-photothermal antibacterial performance against Staphylococcus aureus Under the NIR laser irradiation, if an external magnetic field is introduced, the sterilization effect of Fe 3 O 4 @SiO 2 @Au/PDA nanochains at the same concentration also shows an enhanced effect. During the treatment, Escherichia coli sinks to the bottom of the centrifuge tube due to the action of gravity. In the presence of an external magnetic field, the Fe 3 O 4 @SiO 2 @Au/PDA nanochains are subjected to the Lorentz force in the magnetic field and converge towards the magnetic field (Scheme 1). At this time, there will be a continuous penetrating force on the bacteria. This may be the reason why the sterilization effect is better than that of simple photothermal sterilization. As a result, the Fe 3 O 4 @SiO 2 @Au/PDA nanochains possess a wonderful coupled magnetolytic-photothermal inhibitory effect ( Figure 9). It was found that the Fe 3 O 4 @SiO 2 @Au/PDA nanochains exhibited a unique photothermal effect and thus possess photothermal antibacterial behavior. The magnetic field induced the magnetic nanochains to form a magnetic force which further led to physical damage to the bacteria. As a result, the Fe 3 O 4 @SiO 2 @Au/PDA nanochains possess a coupled magnetic-photothermal antibacterial effect. Here, the magnetic properties of the Fe 3 O 4 @SiO 2 @Au/PDA nanochains do not improve the photothermal property but enhance the antibacterial performance.
Similar to the Escherichia coli, the Fe 3 O 4 @SiO 2 @Au/PDA nanochains also show a coupled magnetolytic-photothermal antibacterial performance against Staphylococcus aureus ( Figure 10). Staphylococcus aureus is a Gram-positive bacteria and a common food-borne pathogen. In recent years, there have been numerous reports of food poisoning caused by Staphylococcus aureus. Therefore, it is very necessary to study the antibacterial properties of Fe 3 O 4 @SiO 2 @Au/PDA nanochains against Staphylococcus aureus. Similar to the results for Escherichia coli, when Fe 3 O 4 @SiO 2 @Au/PDA nanochains are co-cultured with Staphylococcus aureus without other external conditions, Staphylococcus aureus shows a similar growth trend, indicating that the material itself has no killing effect on bacteria. When the Fe 3 O 4 @SiO 2 @Au/PDA nanochain is not added, either treating the solution with 808 nm NIR laser irradiation or a magnetic field, a negative effect on the growth of Staphylococcus aureus is observed, indicating that the Fe 3 O 4 @SiO 2 @Au/PDA nanochain is a main reason for the bactericidal effect. In the NIR laser irradiation alone treatment, the antibacterial effect of the 400 µg/mL sample is significantly better than that of the 200 µg/mL sample, because the higher concentration leads to a better photothermal effect. Similarly, the sterilization effect of Fe 3 O 4 @SiO 2 @Au/PDA nanochains against Staphylococcus aureus at the same concentration is also enhanced when the NIR laser irradiation and a magnetic field are both applied in comparison to the NIR alone. Obviously, the Fe 3 O 4 @SiO 2 @Au/PDA nanochain produces a magnetic force on the Staphylococcus aureus in the presence of an external magnetic field. It was found that this magnetic force is very weak, so the magnetic field alone is not large enough to break the bacteria; thus, the magnetolytic effect cannot be distinguished without applying the NIR irradiation. Under the NIR treatment, the bacteria are inhibited due to the high temperature. Here, the magnetic-field-induced forces improved the antibacterial performance. As a result, the Fe 3 O 4 @SiO 2 @Au/PDA nanochain has a coupled magnetolytic-photothermal antibacterial performance against both Escherichia coli and Staphylococcus aureus (Scheme 1).  Figure 10). Staphylococcus aureus is a Gram-positive bacteria and a common food-borne pathogen. In recent years, there have been numerous reports of food poisoning caused by Staphylococcus aureus. Therefore, it is very necessary to study the antibacterial properties of Fe3O4@SiO2@Au/PDA nanochains against Staphylococcus aureus. Similar to the results for Escherichia coli, when Fe3O4@SiO2@Au/PDA nanochains are co-cultured with Staphylococcus aureus without other external conditions, Staphylococcus aureus shows a similar growth trend, indicating that the material itself has no killing effect on bacteria. When the Fe3O4@SiO2@Au/PDA nanochain is not added, either treating the solution with 808 nm NIR laser irradiation or a magnetic field, a negative effect on the growth of Staphylococcus aureus is observed, indicating that the Fe3O4@SiO2@Au/PDA nanochain is a main reason for the bactericidal effect. In the NIR laser irradiation alone treatment, the antibacterial effect of the 400 μg/mL sample is significantly better than that of the 200 μg/mL sample, because the higher concentration leads to a better photothermal effect. Similarly, the sterilization effect of Fe3O4@SiO2@Au/PDA nanochains against Staphylococcus aureus at the same concentration is also enhanced when the NIR laser irradiation and a magnetic field are both applied in comparison to the NIR alone. Obviously, the Fe3O4@SiO2@Au/PDA nanochain produces a magnetic force on the Staphylococcus aureus in the presence of an external magnetic field. It was found that this magnetic force is very weak, so the magnetic field alone is not large enough to break the bacteria; thus, the magnetolytic effect cannot be distinguished without applying the NIR irradiation. Under the NIR treatment, the bacteria are inhibited due to the high temperature. Here, the magnetic-field-induced forces improved the antibacterial performance. As a result, the Fe3O4@SiO2@Au/PDA nanochain has a coupled magnetolytic-photothermal antibacterial performance against both Escherichia coli and Staphylococcus aureus (Scheme 1).

Conclusions
This work reports a core/shell structured Fe3O4@SiO2@Au/PDA nanochains which exhibit a coupled magnetolytic-photothermal antibacterial performance. Using an Fe3O4 nanochain as the template, the Fe3O4@SiO2@Au/PDA nanochain is prepared with a simple

Conclusions
This work reports a core/shell structured Fe 3 O 4 @SiO 2 @Au/PDA nanochains which exhibit a coupled magnetolytic-photothermal antibacterial performance. Using an Fe 3 O 4 nanochain as the template, the Fe 3 O 4 @SiO 2 @Au/PDA nanochain is prepared with a simple SiO 2 coating and a subsequent in situ redox-oxidization polymerization of an Au/PDA layer. Owing to the presence of Au and PDA, the Fe 3 O 4 @SiO 2 @Au/PDA nanochain possesses a good photothermal property. The Fe 3 O 4 also endows the Fe 3 O 4 @SiO 2 @Au/PDA nanochain with soft magnetic characteristics. With the application of NIR irradiation, the Fe 3 O 4 @SiO 2 @Au/PDA nanochain shows excellent antibacterial performance against both Escherichia coli and Staphylococcus aureus due to the photothermal effect. Interestingly, the magnetic field induces an additional breakage of the bacteria and thus further improves the inhibitory performance. As a result, the Fe 3 O 4 @SiO 2 @Au/PDA nanochain has a coupled magnetolytic-photothermal antibacterial performance against both Escherichia coli and Staphylococcus aureus. In considering biocompatible surfaces, this kind of material possesses a wide potential for future antibacterial substances and nanomedicine.