Photothermal Sensitive 3D Printed Biodegradable Polyester Scaffolds with Polydopamine Coating for Bone Tissue Engineering

Biodegradable scaffolds with photothermal effects and customizable pore structures are a hot topic of research in the field of bone repair. In this study, we prepared porous scaffolds using poly(lactic acid) (PLA) as the raw material and customized the pore structure with 3D printing technology. First, we investigated the effect of pore structure on the mechanical properties of this 3D PLA scaffold. Subsequently, the optimally designed PLA scaffolds were coated with PDA to enhance their hydrophilicity and bioactivity. XRD (X-ray diffraction), FTIR (Fourier transform infrared spectroscopy) and EDS (Energy dispersive spectroscopy) results indicated that PDA was successfully coated on the surface of PLA scaffolds. SEM (Scanning electron microscopy) micrographs showed that the surface of the PDA/PLA scaffolds became rough. WCA (water contact angle) confirmed that the material has enhanced hydrophilic properties. PDA/PLA scaffolds exhibit a tunable photothermal effect under NIR (near infrared) irradiation. The 3D-printed PLA/PDA scaffolds have remarkable potential as an alternative material for repairing bone defects.


Introduction
Bone disorders are of significant concern due to an increase in the median age of the population [1]. In daily life, severe trauma and accidents can lead to severe bone defects, resulting in severe disability that greatly interferes with the patient's life quality [2]. To solve this problem, bone tissue engineering scaffolds have attracted considerable attention because they can provide extracellular matrix and structural support for bone reconstruction and regeneration [3]. Developing a type of bone scaffold with excellent osteoinductivity and programmable pore structure is the current research focus [4]. Several advanced and efficient manufacturing methods are used to manufacture porous biomaterials, such as self-assembly [5,6] and electrospinning [7]. However, most methods for obtaining scaffolds suffer from disadvantages such as poor pore structure and interconnectivity, long subsequent processing steps, and difficulty in rapidly preparing patient-specific scaffolds [8][9][10]. Compared with other methods, the most significant advantage of 3D printing technology based on fused deposition modeling (FDM) is the ability to fabricate custom shapes with an interior lattice network connecting them. They could provide a personalized porous structure that traditional manufacturing techniques cannot adequately attribute, which allows it can programmatically edit and design bone scaffolds with porous structures that can be precisely shaped. These structures are being used for direct implantation into the human body in the biomedical field in areas such as bio-printing, where this potential is being heavily utilized [11]. FDM works by the extrusion of small beads or polymer is suitable for cell adhesion to the transmission was designed and fabricated using PLA as polymer matrix by 3D printing. To enhance the bioactivity of bone scaffolds and further explore more surface modifications, we adopted the abovementioned approach to coat poly(dopamine) on PLA scaffolds (Figure 1a). The chemical composition, morphology, microstructure, and wettability of PDA/PLA porous scaffolds were characterized and analyzed. The biocompatibility of the materials was evaluated by in vitro degradation and in vitro mineralization. Near-infrared irradiation was used to evaluate the photothermal effect of the scaffolds. This material is expected to be an alternative material for bone tissue engineering scaffolds. avoid bacterial infection during surgery, and the inflammatory reaction after surgery and can be used in cancer photothermal therapy [37].
In this work, we aimed to develop a customized biomimetic design for the internal structure of the patient's bone defect area, therefore, a 3D porous bone scaffold model that is suitable for cell adhesion to the transmission was designed and fabricated using PLA as polymer matrix by 3D printing. To enhance the bioactivity of bone scaffolds and further explore more surface modifications, we adopted the abovementioned approach to coat poly(dopamine) on PLA scaffolds (Figure 1a). The chemical composition, morphology, microstructure, and wettability of PDA/PLA porous scaffolds were characterized and analyzed. The biocompatibility of the materials was evaluated by in vitro degradation and in vitro mineralization. Near-infrared irradiation was used to evaluate the photothermal effect of the scaffolds. This material is expected to be an alternative material for bone tissue engineering scaffolds.

Preparation of PLA/PDA Scaffolds
Three-dimensional models were first designed using Solidworks 2012, and then the Hori Z300 plus 3D printer (Hori, China) was used to fabricate 3D scaffolds. In the 3D printing machine, a cartridge was used to supply the feedstock filament of PLA (Hori, China) into the fused deposition modeling (FDM) 3D printer.
3-Hydroxytyramine hydrochloride (dopamine hydrochloride) was dissolved in 10 mM Tris buffer (pH 8.5) to 1 mg mL −1 . All scaffolds were rinsed with deionized water before poly(dopamine) deposition. Polymer scaffolds were soaked in 100 μL of dopamine solution at room temperature for various periods. Meanwhile, the scaffolds were stirred under light-proof and airtight conditions. The prepared scaffolds were named PDA/PLAxh, where x stands for the duration of immersion.

Preparation of PLA/PDA Scaffolds
Three-dimensional models were first designed using Solidworks 2012, and then the Hori Z300 plus 3D printer (Hori, China) was used to fabricate 3D scaffolds. In the 3D printing machine, a cartridge was used to supply the feedstock filament of PLA (Hori, China) into the fused deposition modeling (FDM) 3D printer.
3-Hydroxytyramine hydrochloride (dopamine hydrochloride) was dissolved in 10 mM Tris buffer (pH 8.5) to 1 mg mL −1 . All scaffolds were rinsed with deionized water before poly(dopamine) deposition. Polymer scaffolds were soaked in 100 µL of dopamine solution at room temperature for various periods. Meanwhile, the scaffolds were stirred under light-proof and airtight conditions. The prepared scaffolds were named PDA/PLA-xh, where x stands for the duration of immersion.

Physio-Chemical Characterization
Fourier transform infrared (FTIR) analysis was performed in the wavenumber range of 400-4000 cm −1 with 64 scans per spectrum at 4 cm −1 resolution (FTIR, TENSOR-27, Bruker, Germany). Wide angle X-ray scattering (WAXS) was carried out with a step size of 0.07 • at a scanning speed of 0.3 • s −1 with Cu-Kα radiation in the 2θ range of 5-70 • using an X-ray diffractometer (XRD) (DX-2700, China Fangyuan Instrument Co., Ltd., Hongkong, China) operating at 40 kV and 25 mA. The microstructure morphology of the composite scaffolds was analyzed by field emission scanning electron microscopy (FE-SEM, INSPECTF50, FEI, Holland) at an accelerating voltage of 10 kV. Mechanical testing: The mechanical properties of porous composite scaffolds were determined using an electronic universal testing machine (MIT-30KN, Changzhou SFMIT apparatus Co., Ltd., Changzhou, China), and scaffold samples (10 mm × 10 mm × 5 mm) with the same composition were subjected to each test at room temperature, 65% RH and a crosshead speed of 1.0 mm min −1 to obtain an average value. The contact angle can be used to measure the hydrophilicity of the material. The contact angle of the sample was measured by an SDC-200 contact angle tester (Dongguan Shengding Precision Instrument Co., Ltd., Ruian, China). The material was made into a 40 mm × 40 mm × 5 mm sample, 2 µL water droplets were deposited on the surface of the material using deionized water as the medium, and images were captured by the tester. Three parallel samples were set for each sample, and their average value was taken.

Degradation In Vitro
Degradation test composites were determined by quantification of the mass loss of samples (three different pore size scaffolds) after incubation in PBS at body temperature (37 • C). The medium was exchanged for PBS solution every 6 days to prevent saturation. At the same time, the samples were removed, rinsed with distilled water, weighed after drying at 60 • C for 1 day, and returned to the medium after weighing. The liquor change, drying, and weighing processes were repeated three days at a time. Each group of samples was independently analyzed in three experiments, and the test results were averaged. The degradation rate of the scaffold was calculated with the following formula: where W 0 represents the initial weight of the material and W 1 represents the remaining weight of the sample at different times.

Mineralization In Vitro
Simulated body fluid (SBF, pH = 7.4) was used to evaluate the mineralization behavior of porous composite scaffolds in vitro. Each porous PLA/PDA scaffold with different soaking times was soaked in 20 mL of SBF and then placed in a 37 • C water bath for 7 days. After the immersion ended, the porous composite scaffolds were removed from the SBF and dried under a vacuum for SEM observation.

Near Infrared Test
A near-infrared laser transmitter was used to examine the photothermal conversion effect of PLA/PDA scaffolds with different immersion times. These NIR experiments were performed using a laser transmitter with a wavelength of 808 nm (HW808AD2000-34F, Shenzhen Infrared Laser Technology Co., Ltd., Shenzhen, China). The irradiation distance was 0.3 m, and the spot size was 2 cm.

Statistical Analysis
All data are expressed as the means ± standard deviations (SD) with Origin 2021 (OriginLab, Northampton, MA, USA). A Student's t-test was used to assess the statistical significance of the data between groups, and a value of p < 0.05 was considered to be statistically significant.

Analysis of the Optimal Pore Structure
Bone tissue engineering scaffolds require appropriate mechanical properties to provide mechanical support [38]. However, the microstructure (porosity and pore size) of scaffolds has a nonnegligible effect on their mechanical properties [39]. Therefore, the effect of the pore structure of the scaffold on the performance was studied before the PDA-modified PLA scaffold. Figure 2 shows that the different pore sizes all presented high mechanical properties, and the pore size has little effect on the compressive strength of the scaffolds. But it has been reported that the pore size of scaffolds has a large effect on the proliferation and adhesion of cells. For instance, Cove et al. designed PLA porous scaffolds with pore sizes of 300, 600, and 900 µm and functionalized the scaffolds with a collagen coating. After seven days, the scaffolds with pore sizes of 600 µm exhibited relatively higher cell proliferation and adhesion than those with pore sizes of 300 and 900 µm [40]. Inspired by this work, the pore size of the porous scaffolds was determined to be 600 µm. High porosity scaffolds can promote cell migration and nutrient transport [41]. With constant pore size (600 µm), the scaffolds are designed with different porosity (69%, 74%, 89%). Moreover, the compressive strength of high porosity scaffolds was much lower (0.99 GPa). Therefore, the optimal pore structure of the scaffold was fixed to an average pore size of 600 µm and 74% porosity. Finally, the porous bone scaffold was successfully prepared by soaking PDA. , x FOR PEER REVIEW 5 of 14

Analysis of the Optimal Pore Structure
Bone tissue engineering scaffolds require appropriate mechanical properties to provide mechanical support [38]. However, the microstructure (porosity and pore size) of scaffolds has a nonnegligible effect on their mechanical properties [39]. Therefore, the effect of the pore structure of the scaffold on the performance was studied before the PDAmodified PLA scaffold. Figure 2 shows that the different pore sizes all presented high mechanical properties, and the pore size has little effect on the compressive strength of the scaffolds. But it has been reported that the pore size of scaffolds has a large effect on the proliferation and adhesion of cells. For instance, Cove et al. designed PLA porous scaffolds with pore sizes of 300, 600, and 900 μm and functionalized the scaffolds with a collagen coating. After seven days, the scaffolds with pore sizes of 600 μm exhibited relatively higher cell proliferation and adhesion than those with pore sizes of 300 and 900 μm [40]. Inspired by this work, the pore size of the porous scaffolds was determined to be 600 μm. High porosity scaffolds can promote cell migration and nutrient transport [41]. With constant pore size (600 μm), the scaffolds are designed with different porosity (69%, 74%, 89%). Moreover, the compressive strength of high porosity scaffolds was much lower (0.99 GPa). Therefore, the optimal pore structure of the scaffold was fixed to an average pore size of 600 μm and 74% porosity. Finally, the porous bone scaffold was successfully prepared by soaking PDA.

Analysis of Fourier Transform Infrared Spectroscopy
As shown in Figure 1a, the preparation process of PDA/PLA scaffolds was demonstrated. Meanwhile, Figure 1b shows that the surface of PLA/PDA scaffolds became darker as the soaking time increased. It is observed that the white PLA scaffold soaked with too much amine was attached to a black substance, which was formed by the oxidative self-polymerization of dopamine. This phenomenon can be preliminarily identified as poly(dopamine) being coated on the surface of the material. In the FTIR spectrum shown in Figure 3, which demonstrates that a broad -OH stretching band associated with the polymeric hydrogen bonds of PDA, can be observed in the range of 3200-3400 cm −1 . C-H stretching vibration peaks with -CH3 and -CH-can be observed at approximately 2990 cm −1 . The infrared absorption band of the C=O group of PLA shifts to approximately 1750 cm −1 . Meanwhile, it is noted that the absorption bands of PDA/PLA are shifted to approximately 1077.20 cm −1 , which is due to the stretching vibration of single bond H and the stretching vibration of single bond O stretching and C-O-C in the esterbased structure [42]. For the modified PDA/PLA scaffold, new peaks were observed at 1451.43 cm −1 , which correspond to the characteristic functional groups in PDA [43]. These results indicate that PDA was successfully immobilized on the surface of the PLA scaffold.

Analysis of Fourier Transform Infrared Spectroscopy
As shown in Figure 1a, the preparation process of PDA/PLA scaffolds was demonstrated. Meanwhile, Figure 1b shows that the surface of PLA/PDA scaffolds became darker as the soaking time increased. It is observed that the white PLA scaffold soaked with too much amine was attached to a black substance, which was formed by the oxidative self-polymerization of dopamine. This phenomenon can be preliminarily identified as poly(dopamine) being coated on the surface of the material. In the FTIR spectrum shown in Figure 3, which demonstrates that a broad -OH stretching band associated with the polymeric hydrogen bonds of PDA, can be observed in the range of 3200-3400 cm −1 . C-H stretching vibration peaks with -CH 3 and -CH-can be observed at approximately 2990 cm −1 . The infrared absorption band of the C=O group of PLA shifts to approximately 1750 cm −1 . Meanwhile, it is noted that the absorption bands of PDA/PLA are shifted to approximately 1077.20 cm −1 , which is due to the stretching vibration of single bond H and the stretching vibration of single bond O stretching and C-O-C in the ester-based structure [42]. For the modified PDA/PLA scaffold, new peaks were observed at 1451.43 cm −1 , which correspond to the characteristic functional groups in PDA [43]. These results indicate that PDA was successfully immobilized on the surface of the PLA scaffold.   Figure 4 of XRD shows that there is no peak corresponding to PDA, which is due to the relatively small amount of dopamine hydrochloride added [44]. However, the diffraction peak shown in the figure is consistent with the crystallization peak of pure PLA at approximately 17°, which can be inferred to be the characteristic peak of PLA [45]. The addition of the PDA coating did not change the crystal structure of PLA, and no new diffraction peaks appeared.   Figure 4 of XRD shows that there is no peak corresponding to PDA, which is due to the relatively small amount of dopamine hydrochloride added [44]. However, the diffraction peak shown in the figure is consistent with the crystallization peak of pure PLA at approximately 17 • , which can be inferred to be the characteristic peak of PLA [45]. The addition of the PDA coating did not change the crystal structure of PLA, and no new diffraction peaks appeared.   Figure 4 of XRD shows that there is no peak corresponding to PDA, which is due to the relatively small amount of dopamine hydrochloride added [44]. However, the diffraction peak shown in the figure is consistent with the crystallization peak of pure PLA at approximately 17°, which can be inferred to be the characteristic peak of PLA [45]. The addition of the PDA coating did not change the crystal structure of PLA, and no new diffraction peaks appeared.

Hydrophilicity
Surface wettability has a crucial influence on the initial biological response of scaffolds [46]. The adhesion and proliferation of MSCs could be enhanced on a moderately  [47]. However, PLA is a typical hydrophobic polymeric material that lacks cell recognition signals and has limited applications in biomaterials [48]. The structure of poly(dopamine) contains a large number of phenolic hydroxyl and amino functional groups, and the introduction of poly(dopamine) to PLA scaffolds can effectively improve hydrophilicity and bioactivity. In this study, pure PLA material and PDA/PLA material with different coating times were tested for water contact angle, and the results are shown in Figure 5. The results demonstrate that the water contact angle of pure PLA scaffold material is 75.7 • , which may be related to the pore structure of the scaffold causing droplet drift. Due to the abundance of phenol hydroxy and amino functional groups of poly(dopamine), the hydrophilicity of the PLA scaffold was enhanced. With the gradual increase in polydopamine coating time, the poly(dopamine) coating on the scaffolds continued to increase, resulting in a gradually decreasing trend of the water contact angle of the scaffolds (75.7 • to 63.5 • ). Surface wettability has a crucial influence on the initial biological response of scaffolds [46]. The adhesion and proliferation of MSCs could be enhanced on a moderately hydrophilic surface (water contact angle of 40-80°) [47]. However, PLA is a typical hydrophobic polymeric material that lacks cell recognition signals and has limited applications in biomaterials [48]. The structure of poly(dopamine) contains a large number of phenolic hydroxyl and amino functional groups, and the introduction of poly(dopamine) to PLA scaffolds can effectively improve hydrophilicity and bioactivity. In this study, pure PLA material and PDA/PLA material with different coating times were tested for water contact angle, and the results are shown in Figure 5. The results demonstrate that the water contact angle of pure PLA scaffold material is 75.7°, which may be related to the pore structure of the scaffold causing droplet drift. Due to the abundance of phenol hydroxy and amino functional groups of poly(dopamine), the hydrophilicity of the PLA scaffold was enhanced. With the gradual increase in polydopamine coating time, the poly(dopamine) coating on the scaffolds continued to increase, resulting in a gradually decreasing trend of the water contact angle of the scaffolds (75.7° to 63.5°).

Micromorphology
The pore structure of polylactic acid scaffolds has an important influence on the adhesion, migration, and proliferation of cells in the human body, and the pore size of polylactic acid scaffolds largely determines whether cells can migrate and grow in scaffolds [41]. Figure 6 exhibits the microscopic images of the samples from SEM, showing the morphology of the PDA/PLA scaffold and the morphology of the hole wall surface with different PDA coating times. The abovementioned figure shows that the scaffold maintained a good porous structure, and the surface morphology of the PDA/PLA scaffold was different from that of the pure PLA scaffold. It can be seen that the coating of PDA made the surface of PLA rough, and the longer dopamine immersion time improved the surface roughness of the scaffold. The rough surface could improve the protein adsorption and cell adhesion ability of the materials [49]. In addition, EDS results

Micromorphology
The pore structure of polylactic acid scaffolds has an important influence on the adhesion, migration, and proliferation of cells in the human body, and the pore size of polylactic acid scaffolds largely determines whether cells can migrate and grow in scaffolds [41]. Figure 6 exhibits the microscopic images of the samples from SEM, showing the morphology of the PDA/PLA scaffold and the morphology of the hole wall surface with different PDA coating times. The abovementioned figure shows that the scaffold maintained a good porous structure, and the surface morphology of the PDA/PLA scaffold was different from that of the pure PLA scaffold. It can be seen that the coating of PDA made the surface of PLA rough, and the longer dopamine immersion time improved the surface roughness of the scaffold. The rough surface could improve the protein adsorption and cell adhesion ability of the materials [49]. In addition, EDS results in Figure 7 showed that C, O, and N atoms were evenly distributed on the surface of the scaffold, suggesting that PDA was successfully coated on the surface of the scaffold. in Figure 7 showed that C, O, and N atoms were evenly distributed on the surface of the scaffold, suggesting that PDA was successfully coated on the surface of the scaffold.

Degradation In Vitro
As a biodegradable polymer, poly (lactic acid) (PLA) is commonly used as a scaffold material for repairing tissue defects. The degradation of pure PLA scaffolds and polydopamine-coated PLA scaffolds with different coating times in pH = 7.4 PBS buffer was recorded. Figure 8 shows that pure PLA scaffolds degraded more in the early stage. Due to the large contact-specific surface area of the porous structure, some small molecules were washed out during the PBS soaking process, and the quality was significantly reduced. However, the hydroxyapatite in the PBS buffer solution will be deposited in the inside of the pores of the scaffold and cannot be completely removed, resulting in an increase in mass, which eventually leads to fluctuations in the weight loss rate of the stent. However, in the later stage, the degradation rate became stable and was maintained at a slower rate. After three months of degradation, the quality of the PLA scaffolds decreased by approximately 2.22%, and the total mass of PDA/PLA-4 h decreased by 1.3%. For PDA/PLA-8 h, it was decreased by 0.75%, while for PDA/PLA-12 h, it was decreased by 0.36%. It can be seen that the poly(dopamine) coating layer delays the degradation of the poly(lactic acid) scaffold to a certain extent due to its refractory degradability. However, it has been previously demonstrated that PDA can be taken up by cells and remain stable in major organ cells for several weeks; thus, the insolubility of PDA does not affect its biocompatibility [50]. Degradation of PLA typically occurs through hydrolytic cleavage of ester bonds. In this case, random chain scission leads to a decrease in molecular weight and a rapid decrease in oligomer and monomer content; finally, complete dissolution of the polymer can be observed. The degradation rate of the composite material prepared in this experiment is maintained at a slow level, and the degradation period may be longer; thus, it can be used to repair bone tissue with a long in Figure 7 showed that C, O, and N atoms were evenly distributed on the surface of the scaffold, suggesting that PDA was successfully coated on the surface of the scaffold.

Degradation In Vitro
As a biodegradable polymer, poly (lactic acid) (PLA) is commonly used as a scaffold material for repairing tissue defects. The degradation of pure PLA scaffolds and polydopamine-coated PLA scaffolds with different coating times in pH = 7.4 PBS buffer was recorded. Figure 8 shows that pure PLA scaffolds degraded more in the early stage. Due to the large contact-specific surface area of the porous structure, some small molecules were washed out during the PBS soaking process, and the quality was significantly reduced. However, the hydroxyapatite in the PBS buffer solution will be deposited in the inside of the pores of the scaffold and cannot be completely removed, resulting in an increase in mass, which eventually leads to fluctuations in the weight loss rate of the stent. However, in the later stage, the degradation rate became stable and was maintained at a slower rate. After three months of degradation, the quality of the PLA scaffolds decreased by approximately 2.22%, and the total mass of PDA/PLA-4 h decreased by 1.3%. For PDA/PLA-8 h, it was decreased by 0.75%, while for PDA/PLA-12 h, it was decreased by 0.36%. It can be seen that the poly(dopamine) coating layer delays the degradation of the poly(lactic acid) scaffold to a certain extent due to its refractory degradability. However, it has been previously demonstrated that PDA can be taken up by cells and remain stable in major organ cells for several weeks; thus, the insolubility of PDA does not affect its biocompatibility [50]. Degradation of PLA typically occurs through hydrolytic cleavage of ester bonds. In this case, random chain scission leads to a decrease in molecular weight and a rapid decrease in oligomer and monomer content; finally, complete dissolution of the polymer can be observed. The degradation rate of the composite material prepared in this experiment is maintained at a slow level, and the degradation period may be longer; thus, it can be used to repair bone tissue with a long

Degradation In Vitro
As a biodegradable polymer, poly (lactic acid) (PLA) is commonly used as a scaffold material for repairing tissue defects. The degradation of pure PLA scaffolds and polydopamine-coated PLA scaffolds with different coating times in pH = 7.4 PBS buffer was recorded. Figure 8 shows that pure PLA scaffolds degraded more in the early stage. Due to the large contact-specific surface area of the porous structure, some small molecules were washed out during the PBS soaking process, and the quality was significantly reduced. However, the hydroxyapatite in the PBS buffer solution will be deposited in the inside of the pores of the scaffold and cannot be completely removed, resulting in an increase in mass, which eventually leads to fluctuations in the weight loss rate of the stent. However, in the later stage, the degradation rate became stable and was maintained at a slower rate. After three months of degradation, the quality of the PLA scaffolds decreased by approximately 2.22%, and the total mass of PDA/PLA-4 h decreased by 1.3%. For PDA/PLA-8 h, it was decreased by 0.75%, while for PDA/PLA-12 h, it was decreased by 0.36%. It can be seen that the poly(dopamine) coating layer delays the degradation of the poly(lactic acid) scaffold to a certain extent due to its refractory degradability. However, it has been previously demonstrated that PDA can be taken up by cells and remain stable in major organ cells for several weeks; thus, the insolubility of PDA does not affect its biocompatibility [50]. Degradation of PLA typically occurs through hydrolytic cleavage of ester bonds. In this case, random chain scission leads to a decrease in molecular weight and a rapid decrease in oligomer and monomer content; finally, complete dissolution of the polymer can be observed. The degradation rate of the composite material prepared in this experiment is maintained at a slow level, and the degradation period may be longer; thus, it can be used to repair bone tissue with a long growth cycle and can effectively avoid the degradation caused by rapid material degradation.

Mineralization In Vitro
The ion concentration of simulated body fluid (SBF) is approximately equal to that of human plasma. This PLA/PDA scaffold can form apatite on its surface in the environment of human blood, and this process can be reproduced in SBF. This means that through the formation of mineralized apatite on the SBF surface, the in vivo bioactivity of the material can be predicted [51]. The surface of the porous scaffold shown in Figure 9 demonstrates visible changes after 7 days of SBF soaking, and extensive deposits appeared on the surface of the material. With the increase in the coating time of polydopamine on the surface of the scaffold, the deposition of particles that appeared on the scaffold surface, showed an increasing trend with coating time, which might be hydroxyapatite (HA). In addition, the XRD pattern of PDA/PLA samples after mineralization ( Figure 10) showed that the strength of the PLA crystal peak was weakened, which was caused by the degradation of the scaffold and the deposition of estimated HA on the scaffold. It furtherly proved that PDA/PLA scaffold can promote bone deposition sufficiently. It suggests that the formation of apatite can be improved on the surface of the material due to the excellent biological activity and adhesion properties of poly(dopamine).

Mineralization In Vitro
The ion concentration of simulated body fluid (SBF) is approximately equal to that of human plasma. This PLA/PDA scaffold can form apatite on its surface in the environment of human blood, and this process can be reproduced in SBF. This means that through the formation of mineralized apatite on the SBF surface, the in vivo bioactivity of the material can be predicted [51]. The surface of the porous scaffold shown in Figure 9 demonstrates visible changes after 7 days of SBF soaking, and extensive deposits appeared on the surface of the material. With the increase in the coating time of polydopamine on the surface of the scaffold, the deposition of particles that appeared on the scaffold surface, showed an increasing trend with coating time, which might be hydroxyapatite (HA). In addition, the XRD pattern of PDA/PLA samples after mineralization ( Figure 10) showed that the strength of the PLA crystal peak was weakened, which was caused by the degradation of the scaffold and the deposition of estimated HA on the scaffold. It furtherly proved that PDA/PLA scaffold can promote bone deposition sufficiently. It suggests that the formation of apatite can be improved on the surface of the material due to the excellent biological activity and adhesion properties of poly(dopamine).

Near Infrared Response Test
In Figure 11, it shows the temperature-changing curves of PLA/PDA scaffolds with different immersion times using NIR laser emitter irradiation (0.2 W/cm 2 ) and the critical temperature values are presented. As could be seen, pure PLA samples showed no photothermal effect, other PDA/PLA samples showed a similar trend, i.e., a rapid temperature increase for a relatively short time, followed by a platform of slower heating. When the laser was turned off, the temperature of all samples rapidly cooled in air. With more polydopamine coating, the scaffold heating rate was further accelerated, and the critical temperature of heating was increased from 46.3 • C to 57.6 • C. This efficient photothermal effect is attributed to the uniform coating of PDA on the PLA scaffold. Of note, the temperature of the bone scaffold can be effectively controlled by adjusting the NIR power. It has been demonstrated that the cancer cells can be killed after maintenance at 42 • C for 15-60 min [52], so when conducting photothermal therapy, the heating time and temperature should cause researchers to be wary of causing damage to normal somatic cells. To sum up, the PDA coating makes the PLA/PDA composite scaffold prepared in this work have broad application prospects in the field of photothermal therapy on the basis of excellent biological activity.

Near Infrared Response Test
In Figure 11, it shows the temperature-changing curves of PLA/PDA scaffolds with different immersion times using NIR laser emitter irradiation (0.2 W/cm 2 ) and the critical temperature values are presented. As could be seen, pure PLA samples showed no photothermal effect, other PDA/PLA samples showed a similar trend, i.e., a rapid temperature increase for a relatively short time, followed by a platform of slower heating. When the laser was turned off, the temperature of all samples rapidly cooled in air. With more polydopamine coating, the scaffold heating rate was further accelerated, and the critical temperature of heating was increased from 46.3 °C to 57.6 °C. This efficient photothermal effect is attributed to the uniform coating of PDA on the PLA scaffold. Of note, the temperature of the bone scaffold can be effectively controlled by adjusting the

Near Infrared Response Test
In Figure 11, it shows the temperature-changing curves of PLA/PDA scaffolds with different immersion times using NIR laser emitter irradiation (0.2 W/cm 2 ) and the critical temperature values are presented. As could be seen, pure PLA samples showed no photothermal effect, other PDA/PLA samples showed a similar trend, i.e., a rapid temperature increase for a relatively short time, followed by a platform of slower heating. When the laser was turned off, the temperature of all samples rapidly cooled in air. With more polydopamine coating, the scaffold heating rate was further accelerated, and the critical temperature of heating was increased from 46.3 °C to 57.6 °C. This efficient photothermal effect is attributed to the uniform coating of PDA on the PLA scaffold. Of note, the temperature of the bone scaffold can be effectively controlled by adjusting the NIR power. It has been demonstrated that the cancer cells can be killed after maintenance at 42 °C for 15-60 min [52], so when conducting photothermal therapy, the heating time and temperature should cause researchers to be wary of causing damage to normal somatic cells. To sum up, the PDA coating makes the PLA/PDA composite scaffold prepared in this work have broad application prospects in the field of photothermal therapy on the basis of excellent biological activity.

Conclusions
In this study, a light-sensitive biodegradable surface modified PLA scaffold was designed and fabricated using 3D printing and 3D modeling software. The developed PLA scaffolds were designed of an average pore size of 600 μm a porosity of 74%. By soaking the scaffold in dopamine hydrochloride solution and using the selfpolymerization reaction of dopamine, the PLA surface was surface functionalized with a polydopamine coating, resulting in a good biological activity of bone engineering. XRD and FTIR results indicated that PDA was successfully coated on the surface of PLA scaffolds. SEM micrographs showed that the surface of the PDA/PLA scaffolds became rough due to the surface coating. After 12 h of PDA immersion, the contact angle of the scaffolds decreased from 75.7° to 63.5°, which shows the improvement of hydrophilicity that can promote cell adhesion. PDA/PLA scaffolds exhibit a tunable photothermal effect under NIR irradiation, and the maximum saturation temperature is 57.8 °C, which means that PDA-coated PLA scaffolds have great potential to be used in photothermal therapy. The 3D-printed PLA/PDA scaffolds have remarkable potential as an alternative material for repairing bone defects.

Conclusions
In this study, a light-sensitive biodegradable surface modified PLA scaffold was designed and fabricated using 3D printing and 3D modeling software. The developed PLA scaffolds were designed of an average pore size of 600 µm a porosity of 74%. By soaking the scaffold in dopamine hydrochloride solution and using the self-polymerization reaction of dopamine, the PLA surface was surface functionalized with a polydopamine coating, resulting in a good biological activity of bone engineering. XRD and FTIR results indicated that PDA was successfully coated on the surface of PLA scaffolds. SEM micrographs showed that the surface of the PDA/PLA scaffolds became rough due to the surface coating. After 12 h of PDA immersion, the contact angle of the scaffolds decreased from 75.7 • to 63.5 • , which shows the improvement of hydrophilicity that can promote cell adhesion. PDA/PLA scaffolds exhibit a tunable photothermal effect under NIR irradiation, and the maximum saturation temperature is 57.8 • C, which means that PDA-coated PLA scaffolds have great potential to be used in photothermal therapy. The 3D-printed PLA/PDA scaffolds have remarkable potential as an alternative material for repairing bone defects.

Conflicts of Interest:
The authors declare no conflict of interest.