1. Introduction
The regeneration of bone defects caused by infection or trauma is an important goal in clinical practice, and tissue engineering has been used to control the process of wound healing so that the tissue can be regenerated. The three crucial factors in tissue engineering are cells, scaffold (supporting matrices), and signaling molecules. In terms of the scaffold, hydroxyapatite (HA) is a bone material with osteoconductivity [
1]. The porous structure of HA promotes the ingrowth of cells and microvessel growth leading to bone formation. Moreover, for this bone material, optimal pore sizes from 150 to 500 μm are an important factor in forming new bone [
2].
Even though the adhesion of osteoblast cells to the surface of a scaffold is a crucial factor for the healing of hard tissue, many materials, such as HA or titanium, have a disadvantage in the initial healing process because of their hydrophilicity. To solve this problem, previously, TiO
2 and UV treatments of the surface of materials were adopted. For example, there is biocompatibility based on the formation of a thin TiO
2 layer [
3]. It has been reported that treatment of the surface of dental implants with TiO
2 improves cell adhesion and osseointegration. Fujibayashi and his colleagues [
4] reported in their study on porous titanium material that the complex interconnective macroporous structure improves osteoconductivity. However, titanium and these alloys have been reported to have disadvantages such as low tissue adherence and a degree of toxicity caused by release during corrosion [
5,
6]. Niska and her colleagues [
7] demonstrated that toxicity induced by TiO
2 nanoparticles cause oxidative damage by increasing levels of O
2•− (superoxide anion) in human osteoblast cells. On the other hand, Mani et al. [
8] reported in their in vivo study that hydroxyapatite attenuates the toxicity of TiO
2. In addition, Okumura et al. [
9] studied the initial attachment of osteoblast cells (Saos-2) to different materials, and they reported superior early adhesion of human osteoblast-like cells to HA and titanium than to other materials. Therefore, a combination of HA and TiO
2 for bone regeneration is considered appropriate.
According to several reports on how the surface properties of dental implants improve osseointegration, titanium and these alloys do not show reliable bone-to-implant contact [
4,
10]. They concluded that modifying surface characteristics is necessary to improve osseointegration. Zhao and his colleagues [
11] reported in their study that osteoblasts cultured on hydrophilic surfaces express higher levels of differentiation markers, such as alkaline phosphatase and osteocalcin and generated an osteogenic microenvironment. Ultraviolet (UV) photofunctionalization has been widely studied as a means to increase hydrophilicity to further improve the effect of a scaffold on bone formation [
12,
13,
14]. Radiating the titanium surface with UV enhances the physical properties. One review reported that the unique alteration of the titanium surface after UV treatment is attributed to the surface of TiO
2, which is changed to hydrophilic at the atomic level [
13]. More specifically, UV irradiation of the titanium surface converts Ti
4+ into Ti
3+, which is beneficial for adsorption and makes the titanium surface bioactive by becoming hydrophilic. Thus, in several studies, UV photofunctionalization has been reported as a method for increasing cell attachment and new bone formation to this more hydrophilic surface [
12,
15,
16]. The use of scaffold carriers with increased hydrophilicity is expected to further enhance the initial healing response for regeneration, including angiogenesis and osseointegration.
To reduce nanotoxicity due to nanosized TiO2 particles, we have attempted to lower the ratio of TiO2 by adding a surfactant. An in vitro pilot study indicated that a rapid change in terms of hydrophilicity occurs when concentration of nanosized TiO2 is varied from 1.5 to 5%, as indicated by the change in the contact angle. Therefore, in this study, UV photofunctionalization was examined in 5% TiO2 to determine the minimum dose. This experiment was designed to evaluate the effect of using HA with 5% TiO2 on rabbit calvarial defect models as a bone graft material and to perform histologic and histomorphometric comparisons of the effect of ultraviolet photofunctionalization on new bone formation in the early phase of the healing response.
3. Discussion
The aim of this study was to compare the histological and histomorphometric evaluations of the degree of new bone formation in rabbit calvarial defects when applying HA with 5% TiO
2 and ultraviolet irradiation to induce bone formation. As mentioned above, the contact angle for the hydrophilicity evaluation changes according to the TiO
2 concentration in HA, and hence a concentration of 5% TiO
2 in HA was used in with or without the UV irradiation condition. Moreover, the defect size was 8 mm, which is the critical size requiring additional treatment because the defect will not heal naturally during the life of the animal. Histologic evaluations at two and eight weeks were planned to examine the initial healing response [
17,
18].
Following the grafting of HA with 5% TiO
2, new bone formation was significant at the 2nd and 8th weeks of healing compared to that when only HA was applied. Specifically, the TiO
2-coated HA group and UV treatment group had significantly more new bone formation at two and eight weeks compared with that in the HA only group. This indicated that the effect of TiO
2 on new bone formation was stronger in the initial healing reaction. This may support the results of a study that reported that the nanoscale anodized titanium surface affects cell differentiation in the initial healing period, thus accelerating osseointegration and bone boding strength [
19].
When new bone formation was compared between the TiO
2-coated HA with UV group and TiO
2-coated HA group, the percentage of new bone formation was significantly higher in the UV-irradiated group. The higher level of new bone formation in the UV-treated group was probably due to the electron excitation effect of the UV irradiation on TiO
2 mentioned above. Shen et al. [
14] investigated the effect of UV irradiation on the bone response in the tibial metaphyses and femoral condyle of rabbits in a histological and histomorphometric study. It had been reported that the nanostructure and UV treatment enhance the interfacial strength of titanium and intergranular bone to improve osseointegration. This conclusion is supported by the results of this experiment, despite the fact that different sites were evaluated, although the same experimental animals were used.
For this experiment, UV irradiation was performed for 1 min. In many studies, longer UV exposure times result in a more hydrophilic surface because of photofunctionalization. M. Q. Tran and his colleague [
20] reported that when irradiating with UV for 30 min, the transition from a superhydrophobic to superhydrophilic state occurs faster than with TiO
2 nanoparticle-coated samples. In addition, a superhemophilic pattern was observed in a wettability test on blood, indicating that the UV irradiation had a potential effect on the clinical application [
21]. In a study of the photoinduced hydrophilicity effect, the water contact angle was 54.5° for TiO
2 film without any treatment and 29.3° for 1 min of UV exposure [
22]. For irradiation over 10 min, the result was less than 5°, which indicates superhydrophilicity. However, when the initial healing response indicators such as fibrinogen adsorption and platelet adhesion/spreading were evaluated, there was no significant difference between 1 min and 10 min of UV irradiation; thus, it was concluded that further study was needed. Most other studies have reported that longer irradiation times result in a greater hydrophilic effect by photofunctionalization [
15,
23,
24,
25]. However, for clinical use, it is not appropriate to subject the patient to long treatment times, and hence we set a time of 1 min for this study. Additional studies on light irradiation methods will be needed to develop more appropriate clinical applications.
In this study, a heating technique was used to prevent TiO2 nanoparticles, which were coated homogeneously on the HA surface, from being separated. In other words, this heating technique, involving heating in a furnace to 450 °C, can prevent the separation phenomenon from occurring during the conventional method of mixing TiO2 nanoparticles with HA in ethanol solvent and stirring the mixture ultrasonically. Surface hydrophilicity was evaluated by assessing the contact angle and performing wettability tests, and SEM, XRD, and FTIR measurements were used to detect changes in surface morphology. It was confirmed in SEM and XRD analyses that TiO2 was adsorbed uniformly and stably on the surface of HA. Moreover, because SDBS was not present in the FTIR analysis, the biocompatibility of the corresponding sample might be guaranteed. Based on these results, this process was considered to be a suitable method for coating TiO2 nanopowder on porous HA.
However, the sample size of the TiO
2-coated HA particles changed during the process of ultrasonic dispersion. The pore size of the commercial porous HA (Bongros; Daewoong Pharmaceutical Co. Ltd., Seongnam, Korea) was 300 μm, but the mixed graft material changed to a powder form during the stirring process; thus, the particle size and pore size may have decreased. In a study that evaluated the amount of new bone formation after applying various particle sizes of HA to temporal bullae in rats, larger HA particles were associated with faster new bone formation rates [
26]. This finding explains why the rate of new bone formation was lower in this experiment when using a sample with smaller particle size than the rate reported in our previous study. Chang et al. studied the osteoconductivity of HA samples with various sizes of cylindrical pores, and they reported that active osteoconduction was also observed in HA with 50-μm cylindrical pores [
27]. This can explain the osteoconductivity seen in this experiment, in which the pore size might have decreased. However, further studies on how this affected bone regeneration are needed before conclusions regarding the clinical evaluation and usefulness of the material can be made.
4. Materials and Methods
4.1. Preparation of Bone Graft Materials
Porous HA (Bongros; Daewoong Pharmaceutical Co. Ltd., Seongnam, Korea) was used for this study as a bone graft material. Sodium dodecylbenzenesulfonate (SDBS) was used as a surfactant to enhance the dispersibility of TiO2 nanoparticles on the HA surface. First, 0.2 g of SDBS was completely dissolved in 20 mL of deionized water, and 0.01 g of TiO2 nanoparticles was added to the solution under continuous stirring at 200 rpm for 20 min. Then, 0.2 g of HA and TiO2/SDBS powders, which were obtained from the centrifugation process, were thoroughly stirred into 20 mL ethanol for 20 min. After that, heat treatment at 450°C for 3 h was applied to the mixture (mixing ratio: HA 0.2 g, TiO2 0.01 g) to remove volatile SDBS.
The microscopic surface structures of porous HA and TiO2-coated HA were analyzed using scanning electron microscopy (SU8220, Hitachi High Technologies, Tokyo, Japan) following the platinum coating of the samples. The quantitative and qualitative measurements for the structural identification of the graft material compositions were performed using an energy dispersive X-ray spectrometer (X-ManN50 011; HORIBA, Kyoto, Japan).
4.2. Wettability Test
To evaluate hydrophilicity, a wettability test was performed to measure the contact angle of water droplets (interval time: 3 min) with HA and a certain amount of TiO2 coated on HA. All the procedures were carried out in a class 10 clean room under the conditions of 20°C and 46% humidity.
4.3. UV Photofunctionalization
Photofunctionalization was performed by irradiating the HA graft materials containing TiO2 with UV light in a dark room for 1 min using a photo device immediately before grafting. Specifically, the UV treatment was performed at room temperature for a fixed distance of 3 cm between the sample (the irradiated area on the sample was 2 × 2 cm2) and the UV light source (UV radiation with a peak at 253.7 nm, power: 8 W).
4.4. Animal Study
Twelve New Zealand white rabbits weighing 2.7 to 3.2 kg were used in this study. The animals were fed a standard diet and housed in separate cages under standard laboratory conditions. This experiment, including animal selection, management, and the surgery protocol, was approved by the Institutional Animal Care and Use Committee of Kyungpook National University, Daegu, Korea (certification #2017-0094; 05/07/2017). General anesthesia was induced by intramuscular injection of a mixture of zolazepam (0.2 mL/kg; Zoletil, Virbac, Carros, France) and xylazine (0.25 mL/kg; Rompun, Bayer Korea Co., Seoul, Korea). The surgical site was shaved and then covered with alcohol and povidone iodine. Complementary infiltrative anesthesia was administrated at the surgical site using 2% lidocaine with 1/100,000 epinephrine (1:100,000 epinephrine; Yuhan Co., Seoul, Korea) to control bleeding. The surgical site was exposed with a sagittal midline incision through the skin and the periosteum at the midline of the calvaria and a full-thickness flap elevation. Four standardized transosseous circular defects (of critical size: diameter 8 mm) were prepared using a stainless steel trephine bur in the frontal and parietal bones of each animal under cool-saline irrigation (
Figure 6a).
Defects were filled with following graft materials (
Figure 6b), 0.025 g of HA, HA group; 0.025 g of TiO
2-coated HA, TiO
2-coated HA group; 0.025 g of TiO
2-coated HA, treated with UV for 1 min, TiO
2-coated HA with UV group; and the last defect was left unfilled as a negative control (NC), NC group. After surgery, surgical defects were covered with a resorbable collagen membrane (collatape; Zimmer, Carlsbad, CA, USA), and the soft tissues were closed in layers and sutured for primary closure using braided polyglycolic acid sutures (5-0 surgifit; AILEE, Busan, Korea) and Monofilament sutures (4-0 nylon; NYLON (blue); AILEE, Busan, Korea). Antibiotics (Baytril, Bayer Korea Co., Seoul, Korea) and analgesics (Nobin, Bayer Korea Co., Seoul, Korea) were injected intramuscularly for 3 days to control pain and prevent postsurgical infection as a postoperative management. Six animals were sacrificed by intravenous injections of air under general anesthesia at 2 weeks postoperatively, and the rest were sacrificed 8 weeks after the surgery. After sacrifice, the area of the surgical defect site and surrounding tissues were removed en bloc. These collected samples were fixed in 4% neutral-buffered paraformaldehyde.
4.5. X-ray Microcomputed Tomography Analysis
First, all en bloc samples were subjected to X-ray microtomography. This protocol micro-CT imaging was performed at the Pohang Center for Evaluation of Biomaterials, Pohang Technopark in Pohang, Korea, using a Siemens Inveon Trimodality Image system (INVEON; Siemens, Washington, DC, USA).
The CT slice images were reconstructed using Siemens Inveon Acquisition Workplace Software (INVEON; Siemens, Washington, DC, USA). CT Acquisition: For a whole body CT scan, set current at 500 uA, voltage at 80 kV, exposure time at 280 msec, and 180 steps for 360° rotation. For X-ray detector, select resolution at “low system magnification” with 57.6 mm axial imaging field and single bed mode. We selected “real time reconstruction” using the “Common Cone-Beam Reconstruction” method so that the host PC talks with a dedicated real timereconstruction computer (Cobra) to initiate the task. The corresponding images, produced by stacking all cross-sectional images, create a map of the local X-ray attenuation coefficient plus the enhanced boundaries by the interference of transmitting coherent X-rays. Image analysis software (Amira Version 6.2; FEI Co., Hillsboro, OR, USA) was used for tridimensional (3D) visualization. In the image analysis, newly formed bone fragments were clearly distinguished from the HA in the gray level. Analysis of the 3D images allowed calculating the regenerated total volume of surgical defects and the extent of the newly formed radiopaque area at two weeks and eight weeks postoperatively.
4.6. Surface Characteristics and Histological and Histomorphometric Analyses
For histological analysis, the fixed samples were decalcified in 10% ethylenediaminetetraacetic acid (EDTA) for 1 month and then embedded in paraffin. The paraffin-embedded tissues were cut from the center at 3-µm intervals using a Leica microtome (RM2245; Leica Microsystems, Bannockbrun, IL, USA), and the most central sections from each sample were subjected to hematoxylin-eosin (H&E) and Masson’s trichrome staining. Histological evaluations were performed by observing the stained sections under a microscope (Olympus BX53, Olympus, Tokyo, Japan) equipped with a 10 × 0.30 UPLANFL N objective lens (Olympus, Tokyo, Japan). Images were captured using a digital camera (Olympus, Tokyo, Japan) attached to the microscope. Histomorphometric analysis was performed using image analysis software (I-solution; iMTechnology, Daejeon, Korea) to calculate the amount of new bone ingrowth in the defect sites: (1) the percentage of new bone (%) = the area of new bone between the defect margins (mm2)/the total augmented area (mm2) × 100 (%) and (2) the percentage of residual bone material (%) = the area of residual bone material between the defect margins (mm2)/the total augmented area (mm2) × 100 (%).
4.7. Data Analysis
Statistical analyses were conducted using IBM SPSS Statistics (SPSS Inc., Chicago, IL, USA). Statistical analyses included a nonparametric Kruskal–Wallis analysis of variance test to evaluate differences in the percentages of new bone formation and remaining bone particles. The Mann–Whitney U-test was used to evaluate the difference in bone regeneration between groups. Statistical significance was defined as a p-value less than 0.05.