In Vitro Cytotoxicity of Possible Corrosion Products from Mg-Based Biodegradable Metals: Magnesium Oxide and Magnesium Hydroxide Nanoparticles

: Biodegradable magnesium (Mg) alloys have potential applications in orthopedic implants due to their mechanical and osseointegration properties. However, the surface characteristics, biocompatibility, and toxicity of the released corrosion products in the form of magnesium oxide (MgO) and magnesium hydroxide (Mg(OH) 2 ) nanoparticles (NPs) at the junction of implants and in the surrounding tissue are not completely understood. Here, we investigated in vitro cytotoxicity and morphological changes in human fetal osteoblast (hFOB) 1.19 cells in response to various concentrations (1 mM, 5 mM, 10 mM, and 50 mM) of MgO / Mg(OH) 2 NPs by live / dead assay and scanning electron microscopy (SEM). In this study, we performed a surface characterization of MgO / Mg(OH) 2 NPs to evaluate the size of the NPs. Further, an immersion test was performed in Dulbecco’s Modiﬁed Eagle’s Medium (DMEM) with randomly selected various concentrations (1 mM, 5 mM, 10 mM, 50 mM, and 100 mM) of MgO / Mg(OH) 2 NPs to understand the degradation behavior of the NPs, and the change in the pH values from days 1 to 7 was measured. After conducting an immersion test for seven days, the highest concentration (100 mM) of MgO / Mg(OH) 2 NPs was selected to study the element depositions on nanoparticles through scanning electron microscopy–energy-dispersive X-ray spectroscopy (SEM–EDX) mapping. The results from this in vitro cytotoxicity study suggest that less than or equal to 5-mM concentrations of MgO / Mg(OH) 2 NPs are tolerable concentrations for hFOB 1.19 cells. This study provides a foundational knowledge of MgO / Mg(OH) 2 NP cytotoxicity in hFOB 1.19 cells that can help to develop future sustainable biodegradable magnesium-based alloys for orthopedic applications. The morphological changes studied by SEM analysis showed comparable results to the live / dead assay for cell adhesion, proliferation, and cell death. The results from this in vitro cytotoxicity study suggest that less than or equal to 5-mM concentrations of MgO / Mg(OH) 2 NPs are tolerable concentrations for hFOB 1.19 cells. On the basis of this foundational study, in the future, innovative biodegradable Mg-based alloys can be developed for their application in orthopedics. We also suggest that future research must be done to understand the cytotoxicity of corrosion products through a real-time in vitro sensing system and in vivo testing.


Introduction
Orthopedics is a multibillion-dollar global industry that is mainly focused on the diagnosis, treatment, and prevention of musculoskeletal system via surgical and nonsurgical therapeutic interventions. Orthopedic devices have gained a considerable amount of attention for the treatment of

Immersion Test and pH Measurement
We investigated the degradation behavior of the MgO/Mg(OH) 2 NPs through an immersion test. After the sterilization of various concentrations of MgO/Mg(OH) 2 NPs (1 mM, 5 mM, 10 mM, 50 mM, and 100 mM) through ultraviolet (UV) rays for 15 min, samples were immersed in 1 mL of Dulbecco's Modified Eagle's Medium (DMEM) with 4.5 g/L glucose and sodium pyruvate without L-glutamine and phenol red (Cat# 17-205-CV, Cellgro) for 7 days in a 24-well plate. Each sample was carried out in triplicate. Samples were maintained in an Isotemp incubator (ThermoFisher Scientific, NC, USA) under standard cell culture conditions (37 • C, 5% CO 2 ) to study the change in pH from day 1 to 7.
The pH values were measured at time points during days 1-7 using a pH meter (Oakton ® pH2100, Eutech Instruments, Singapore) to understand the degradation behavior of MgO/Mg(OH) 2 NPs.

Surface Morphology and Element Analysis
The surface characteristics of MgO/Mg(OH) 2 NPs were determined by a Hitachi SU8000 Field Emission Scanning Electron Microscope (Hitachi High Technologies America, Dallas, TX) after gold-coating the samples using a Polaron E5400 Sputter coater. This gold coating served as a strain for SEM to enhance the contrast of the images. For effective results, the gold sputter chamber was flushed with argon gas at a low pressure at a direct current (DC) voltage between 1000 and 3000 volts. In addition, after conducting the immersion test for 7 days, samples were gold-coated, and element depositions on the MgO/Mg(OH) 2 NPs were analyzed through EDX Quantax Esprit 1.8.2 software (Bruker). Further, an EDX mapping analysis was performed to evaluate the element distribution on the MgO/Mg(OH) 2 NPs. With the EDX mapping, each element was scanned individually across the entire surface of the MgO/Mg(OH) 2 NPs. An overlay of all the elements distributed on the surface of the MgO/Mg(OH) 2 NPs was observed to predict the presence of the corrosion products.

Cell Culture and Treatment
Human fetal osteoblast (hFOB) 1.19 cells (SV40 large T antigen transfected; American Type Culture Collection) (Cat# ATCC ® CRL-11372™) were cultured in complete growth media (1:1 mixture of Ham's F12 medium with L-glutamine (Cat#10-080-CV, Cellgro) and Dulbecco's Modified Eagle's Medium with 4.5 g/L glucose and sodium pyruvate without L-glutamine and phenol red (Cat# 17-205-CV, Cellgro)) supplemented with 0.3 mg/mL gentamicin sulfate (Cat# 17-518Z, Lonza) and 10% fetal bovine serum (heat-inactivated at 56 • C) (Cat# S1105H, Atlanta Biologicals) under standard cell culture conditions (37 • C, 5% CO 2 ) with humidified air. After the third passage, cells were seeded (50,000 cells/well) in 1 mL of complete growth media on a glass coverslip in a 24-well plate. Further, cells were incubated under standard cell culture conditions (37 • C, 5% CO 2 ) with humidified air for 2-3 days to allow for adhesion to a 24-well plate. Experimental groups received the cells cultured in complete growth media; however, negative control groups received media only and cells cultured in complete growth media. Further, 24-well plates were aspirated.
Various concentrations of MgO/Mg(OH) 2 NPs (1 mM, 5 mM, 10 mM, and 50 mM) were sterilized for 15 min in an ultraviolet (UV) light before exposure to hFOB 1.19 cells to prevent any microbial growth. After sterilization, each concentration of MgO/Mg(OH) 2 NPs was immersed in 1 mL of complete growth media in a 15 mL tube (Cat#05-539-5, Fisher brand). Control groups received 0.5 mL of freshly prepared complete growth media; however, experimental groups received 0.5 mL of various concentrations (1 mM, 5 mM, 10 mM, and 50 mM) of MgO/Mg(OH) 2 NPs prepared in complete growth media on the 24-well plates. Samples were incubated under standard cell culture conditions (37 • C, 5% CO 2 ) with humidified air for 30 min. Each sample was in triplicate for the reproducibility of the results. Further, 24-well plates were aspirated, and samples were rotated slightly in 1X phosphate-buffered saline (PBS) (Cat#21-040-CM, Cellgro) maintained at pH 7.4 to remove nonadherent cells. They were allowed to sit for 10 min at room temperature (RT).

Live/Dead Assay
A Live/Dead ® Viability/Cytotoxicity kit (Cat# L3224, Invitrogen) was utilized to study the cell viability and cytotoxicity in hFOB 1.19 cells in response to various concentrations (1 mM, 5 mM, 10 mM, and 50 mM) of MgO/Mg(OH) 2 NPs. With this two-color fluorescence-based assay, live and dead cells were determined by calcein acetomethoxy (calcein AM) and ethidium homodimer (EthD-1) dyes as a marker for cell viability and intracellular esterase activity and plasma membrane integrity. The intracellular esterase activity through the conversion of nonfluorescent cell-permeable calcein AM to intensified fluorescent calcein determined the live cells. Calcein was retained within the live cells to produce green fluorescence in the live cells (excitation/emission wavelengths of 495/515 nm), whereas EthD-1 entered through the damaged plasma membrane of the cells and showed a 40-fold enrichment of fluorescence upon binding to nucleic acids to produce a bright red fluorescence in dead cells (excitation/emission wavelengths of 495/635 nm).
Samples were allowed to rotate in 1X phosphate-buffered saline (PBS) and sit for 10 min at RT, as mentioned in Section 2.4. Meanwhile, for the preparation of the dye solution, 18 µL EthD-1 was added in 18 mL of PBS, followed by the addition of 18 µL of calcein AM, to achieve 0.5 mL of dye solution per sample in a 24-well plate for MgO/Mg(OH) 2 NPs sample sets. Since each sample was in triplicate, for each sample set, 0.5 mL of freshly prepared dye solution was added slowly in drop-by-drop fashion. The 24-well plates were allowed to sit in the dark for 30-40 minutes, followed by observation under a fluorescence microscope (EVOS XL AMG).
Live (green) and dead (red) cells were counted utilizing Image J software (Version 1.48, National Institutes of Health, Bethesda, Maryland, USA). The percent (%) live cells was calculated as Here, we calculated the total number of cells by adding the number of live cells to the number of dead cells. Further, the results for the percent (%) live cells were analyzed statistically by one-way analysis of variance (ANOVA) techniques using Prism version 5.0 (GraphPad Software, Inc., San Diego, CA, USA). The difference between means was considered statistically significant when the p-value was ≤0.05 when compared to controls. The results obtained were expressed as mean ± standard error (SE) or standard deviation (SD).

Morphological Changes in hFOB 1.19 Cells
A Hitachi SU8000 field emission SEM was utilized to observe morphological changes in the hFOB 1.19 cells in response to various concentrations (1 mM, 5 mM, 10 mM, and 50 mM) of MgO/Mg(OH) 2 NPs. Samples were treated as mentioned in Section 2.4.
Further, samples were rinsed three times with 1X phosphate-buffered saline (PBS) (Cat#21-040-CM, Cellgro) maintained at pH 7.4 to remove any nonadherent cells. The attached hFOB 1.19 cells were fixed in 4% paraformaldehyde (Cat# 19943, Affymetrix) and were left for 15-20 min at RT, followed by aspiration. Further, 1X phosphate-buffered saline (PBS) was added thrice to the samples and was left for 5 min (each at RT), followed by aspiration. Different concentrations of ethanol were prepared in 1X phosphate-buffered saline (PBS): 30%, 50%, 70%, 90%, 95%, and 100%. Each sample was treated with 0.5 mL of each of the prepared concentrations of ethanol, starting from 30% for 5 min, followed by aspiration. Samples were treated with increasing concentrations of ethanol to remove any impurities, if any, before scanning through SEM. Samples were allowed to dry in a chemical fume hood prior to gold-coating on the samples being performed for SEM analysis. Further, an SEM analysis was performed to evaluate morphological changes in the hFOB 1.19 cells.

Results and Discussion
In this study, we investigated in vitro cytotoxicity in hFOB 1.19 cells in response to various concentrations of MgO/Mg(OH) 2 NPs. An immersion test was conducted to study the degradation behavior of various concentrations (1mM, 5mM, 10mM, 50 mM, 100 mM) of MgO/Mg(OH) 2 NPs in DMEM under standard conditions (37 • C, 5% CO 2 ) for 1-7 days. Change in the pH values was measured at time points during days 1-7. After seven days, elemental depositions on MgO/Mg(OH) 2 NPs were analyzed through SEM-EDX analysis. Further, a fluorescence-based live/dead assay was conducted to evaluate the cell viability and cell-mediated cytotoxicity in hFOB 1.19 cells upon exposure to various concentrations (1 mM, 5 mM, 10 mM, and 50 mM) of MgO/Mg(OH) 2 NPs for 30 min. In addition, the morphological characterization of the hFOB 1.19 cells in response to the various concentrations of MgO/Mg(OH) 2 NPs was evaluated using SEM.

Surface Characterization of MgO/Mg(OH) 2 NPs through SEM
The surface topology of MgO/Mg(OH) 2 NPs was analyzed by SEM. The results showed that the average size of the MgO NPs was <50 nM, whereas the average size of the Mg(OH) 2 NPs was <100 nM, as shown in Figures 1 and 2, respectively. The results in Figure 1 confirm that the average particle size of the MgO NPs was <50 nM (particle sizes of 39.69 nM at a 5 µm resolution and 41.67 nM at a 1 µm resolution are shown). However, the average particle size of Mg(OH) 2 NPs was <100 nM (particles sizes of 59.53 nM at a 5 µm resolution and 92.60 nM at a 1 µm resolution are shown), as shown in Figure 2. The color of the MgO/Mg(OH) 2 NPs was white; however, the particles were irregular in shape. A particle size analysis was conducted using Image-Pro Plus based on the SEM image. Briefly, we randomly selected three regions followed by histogram-based particle selection and particle counting.
Further, 1X phosphate-buffered saline (PBS) was added thrice to the samples and was left for 5 min (each at RT), followed by aspiration. Different concentrations of ethanol were prepared in 1X phosphate-buffered saline (PBS): 30%, 50%, 70%, 90%, 95%, and 100%. Each sample was treated with 0.5 ml of each of the prepared concentrations of ethanol, starting from 30% for 5 min, followed by aspiration. Samples were treated with increasing concentrations of ethanol to remove any impurities, if any, before scanning through SEM. Samples were allowed to dry in a chemical fume hood prior to gold-coating on the samples being performed for SEM analysis. Further, an SEM analysis was performed to evaluate morphological changes in the hFOB 1.19 cells.

Results and Discussion
In this study, we investigated in vitro cytotoxicity in hFOB 1.19 cells in response to various concentrations of MgO/Mg(OH)2 NPs. An immersion test was conducted to study the degradation behavior of various concentrations (1mM, 5mM, 10mM, 50 mM, 100 mM) of MgO/Mg(OH)2 NPs in DMEM under standard conditions (37 °C, 5% CO2) for 1-7 days. Change in the pH values was measured at time points during days 1-7. After seven days, elemental depositions on MgO/Mg(OH)2 NPs were analyzed through SEM-EDX analysis. Further, a fluorescence-based live/dead assay was conducted to evaluate the cell viability and cell-mediated cytotoxicity in hFOB 1.19 cells upon exposure to various concentrations (1 mM, 5 mM, 10 mM, and 50 mM) of MgO/Mg(OH)2 NPs for 30 min. In addition, the morphological characterization of the hFOB 1.19 cells in response to the various concentrations of MgO/Mg(OH)2 NPs was evaluated using SEM.

Surface Characterization of MgO/Mg(OH)2 NPs through SEM
The surface topology of MgO/Mg(OH)2 NPs was analyzed by SEM. The results showed that the average size of the MgO NPs was < 50 nM, whereas the average size of the Mg(OH)2 NPs was < 100 nM, as shown in Figures 1 and 2, respectively. The results in Figure 1 confirm that the average particle size of the MgO NPs was < 50 nM (particle sizes of 39.69 nM at a 5 µm resolution and 41.67 nM at a 1 µm resolution are shown). However, the average particle size of Mg(OH)2 NPs was < 100 nM (particles sizes of 59.53 nM at a 5 µm resolution and 92.60 nM at a 1 µm resolution are shown), as shown in Figure 2. The color of the MgO/Mg(OH)2 NPs was white; however, the particles were irregular in shape. A particle size analysis was conducted using Image-Pro Plus based on the SEM image. Briefly, we randomly selected three regions followed by histogram-based particle selection and particle counting.

Change in the pH Values in Response to Various Concentrations of MgO/Mg(OH)2 NPs
The degradation behavior of various concentrations of MgO/Mg(OH)2 NPs was studied in 1 ml of DMEM under standard conditions (37 °C, 5% CO2) to understand the degradation behavior of these corrosion products. The change in the pH values was measured from days 1 to 7. As represented in Figure

Change in the pH Values in Response to Various Concentrations of MgO/Mg(OH) 2 NPs
The degradation behavior of various concentrations of MgO/Mg(OH) 2 NPs was studied in 1 mL of DMEM under standard conditions (37 • C, 5% CO 2 ) to understand the degradation behavior of these corrosion products. The change in the pH values was measured from days 1 to 7. As represented in Figure

Change in the pH Values in Response to Various Concentrations of MgO/Mg(OH)2 NPs
The degradation behavior of various concentrations of MgO/Mg(OH)2 NPs was studied in 1 ml of DMEM under standard conditions (37 °C, 5% CO2) to understand the degradation behavior of these corrosion products. The change in the pH values was measured from days 1 to 7. As represented in Figure  3      The immersion test result showed that the size and concentrations of the MgO/Mg(OH)2 NPs regulated their degradation behavior in DMEM. The higher concentrations of NPs ( >50 mM) showed increased degradation behavior when compared to lower concentrations (<50 mM) and the control groups (no influence on the pH). At higher concentrations, the solution was more alkaline due to the release of an OHion. The release of increased OHions at higher concentrations of MgO/Mg(OH)2 NPs indicates a challenge for future biodegradable Mg-based alloys. The result of this immersion test provides tolerable lower concentrations of MgO/Mg(OH)2 NPs that might be released from the biodegradable Mg-based alloys to help develop innovative alloys for successful implementation in future in vivo testing.

Element Depositions on MgO/Mg(OH)2 NPs after Immersion Test
Elemental depositions on MgO/Mg(OH)2 NPs were determined using SEM-EDX analysis after immersion tests in DMEM. Samples with 100-mM concentrations of MgO/Mg(OH)2 NPs were dried, goldcoated, and analyzed through SEM-EDX analysis. Figure 5 shows the presence of Mg, O, Na, Ca, P, Cl, and K as the corrosion products. Figure 6 shows the presence of Mg, O, Na, Ca, P, Cl, and K as the corrosion products for Mg(OH)2 NPs through SEM-EDX analysis after an immersion test conducted in DMEM for seven days.

Element Depositions on MgO/Mg(OH) 2 NPs after Immersion Test
Elemental depositions on MgO/Mg(OH) 2 NPs were determined using SEM-EDX analysis after immersion tests in DMEM. Samples with 100-mM concentrations of MgO/Mg(OH) 2 NPs were dried, gold-coated, and analyzed through SEM-EDX analysis. Figure 5 shows the presence of Mg, O, Na, Ca, P, Cl, and K as the corrosion products.

The Cell Viability and Cytotoxicity Study in hFOB 1.19 Cells
Cell viability and cytotoxicity in hFOB 1.19 cells in response to various concentrations (1 mM, 5 mM, 10 mM, and 50 mM) of MgO/Mg(OH) 2 NPs were studied through a live/dead assay, as represented in

The Cell Viability and Cytotoxicity Study in hFOB 1.19 Cells
Cell viability and cytotoxicity in hFOB 1.19 cells in response to various concentrations (1 mM, 5 mM, 10 mM, and 50 mM) of MgO/Mg(OH) 2 NPs were studied through a live/dead assay, as represented in Figures 9 and 10

The Cell Viability and Cytotoxicity Study in hFOB 1.19 Cells
Cell viability and cytotoxicity in hFOB 1.19 cells in response to various concentrations (1 mM, 5 mM, 10 mM, and 50 mM) of MgO/Mg(OH) 2 NPs were studied through a live/dead assay, as represented in Figures 9 and 10, respectively. Fluorescence microscope results showed green (live), healthy, and viable hFOB 1.19 cells with a few red (dead) cells upon exposure to lower concentrations (5 mM or less) of MgO/Mg(OH) 2 NPs when compared to the higher concentrations (10 mM or more). The negative control group Figures 9b and 10b results showed green (live), healthy, and viable cells with no red (dead) cells. An increase in competitive red (dead) cells at the higher concentrations indicated cytotoxicity in the cells. Figure 10f

Discussion
In this study, we investigated the exposure of various concentrations (1 mM, 5 mM, 10 mM, and 50 mM) of MgO/Mg(OH)2 NPs in hFOB 1.19 cells to understand in vitro cytotoxicity. The determination of cytotoxicity in response to concentrations of MgO/Mg(OH)2 NPs in hFOB 1.19 cells will help develop sustainable biodegradable alloys as implant materials for commercial orthopedic devices. A recent study showed that the hemostasis of bone is affected by local pH and oxygen tension [22]. Hypoxia inhibits the proliferation and differentiation of the osteoblast cells responsible for bone formation and stimulates osteoclast cells that are associated with bone resorption. In addition, a foundational study on Mg-based implants reported a faster corrosion rate for implants in the physiological environment of the body, which makes it challenging to establish Mg as a biodegradable material [16]. One study also suggested that the

Discussion
In this study, we investigated the exposure of various concentrations (1 mM, 5 mM, 10 mM, and 50 mM) of MgO/Mg(OH)2 NPs in hFOB 1.19 cells to understand in vitro cytotoxicity. The determination of cytotoxicity in response to concentrations of MgO/Mg(OH)2 NPs in hFOB 1.19 cells will help develop sustainable biodegradable alloys as implant materials for commercial orthopedic devices. A recent study showed that the hemostasis of bone is affected by local pH and oxygen tension [22]. Hypoxia inhibits the proliferation and differentiation of the osteoblast cells responsible for bone formation and stimulates osteoclast cells that are associated with bone resorption. In addition, a foundational study on Mg-based implants reported a faster corrosion rate for implants in the physiological environment of the body, which makes it challenging to establish Mg as a biodegradable material [16]. One study also suggested that the

Discussion
In this study, we investigated the exposure of various concentrations (1 mM, 5 mM, 10 mM, and 50 mM) of MgO/Mg(OH) 2 NPs in hFOB 1.19 cells to understand in vitro cytotoxicity. The determination of cytotoxicity in response to concentrations of MgO/Mg(OH) 2 NPs in hFOB 1.19 cells will help develop sustainable biodegradable alloys as implant materials for commercial orthopedic devices. A recent study showed that the hemostasis of bone is affected by local pH and oxygen tension [22]. Hypoxia inhibits the proliferation and differentiation of the osteoblast cells responsible for bone formation and stimulates osteoclast cells that are associated with bone resorption. In addition, a foundational study on Mg-based implants reported a faster corrosion rate for implants in the physiological environment of the body, which makes it challenging to establish Mg as a biodegradable material [16]. One study also suggested that the exposure of corrosion products such as MgO to an aqueous solution leads to the formation of Mg(OH) 2 [19]. Further, the corrosion of Mg(OH) 2 in an aqueous solution containing 150 mmol/L of Cl − forms magnesium chloride (MgCl 2 ) and hydrogen (H 2 ) gas [23]. In this study, we observed the presence of trace amounts of Cl for both MgO and Mg(OH) 2 NPs after conducting the immersion test for seven days, as analyzed through SEM-EDX mapping (shown in Figures 7 and 8). This result suggests the formation of water-soluble MgCl 2 − . The presence of Ca and P indicates that these corrosion products might interact with the Ca and P present in the environment and disintegrate in bulk in the case of implant degradation into the surrounding medium, as explained in the biocorrosion model [24]. These insoluble complex compounds of MgO/Mg(OH) 2 NPs in the form of magnesium phosphates might introduce cytotoxicity into hFOB 1.19 cells, as shown below: The immersion test result showed rapid degradation behavior of MgO/Mg(OH) 2 NPs in DMEM due to the release of more OH − , which was indicated by an increase in the pH values for the concentrations 10 mM, 50 mM, and 100 mM when compared to lower concentrations (1 mM and 5 mM) and the control groups. On the basis of the results of the pH values obtained from the immersion test, we optimized the higher concentration selection to 50 mM, as no significant difference was observed between the 50-mM and 100-mM concentrations. Therefore, selected concentrations of 1 mM, 5 mM, 10 mM, and 50 mM of MgO/Mg(OH) 2 NPs were used for further live/dead assays and SEM analyses to determine cytotoxicity and morphological changes, respectively.
The live/dead assay results showed that upon exposure to lower concentrations (1 mM and 5 mM) of MgO/Mg(OH) 2 NPs in hFOB 1.19 cells, proliferation and adhesion with fewer dead cells was observed. However, upon exposure to higher concentrations (10 mM and 50 mM) of MgO/Mg(OH) 2 NPs, a reduction in cell proliferation in hFOB 1.19 cells was observed. Interestingly, upon exposure to 50-mM concentrations of Mg(OH) 2 NPs in hFOB 1.19 cells, the clustering of cells due to the disruption of plasma membrane integrity and the formation of insoluble complex compounds was observed. Besides, the SEM analyses showed morphological changes in hFOB 1.19 cells upon exposure to various concentrations of MgO/Mg(OH) 2 NPs. The SEM analysis results showed that upon exposure to lower concentrations (1 mM and 5 mM) of MgO/Mg(OH) 2 NPs, cells adhered, proliferated, and elongated; however, at the higher concentrations (10 mM and 50 mM), the morphology of the cells changed to a round structure, thereby indicating the disruption of plasma membrane integrity and cytotoxicity when compared to control groups. The results from the live/dead assays and the SEM analyses, therefore, were comparable in terms of cell adhesion, proliferation, and cell death. Hence, this in vitro study provides a foundational knowledge for an acceptable concentration of MgO/Mg(OH) 2 NPs that might be released from biodegradable Mg-based alloys in their application in orthopedic implants in future in vivo studies.

Conclusions
In this present study, in vitro cytotoxicity in hFOB 1.19 cells in response to various concentrations (1 mM, 5 mM, 10 mM, and 50 mM) of MgO/Mg(OH) 2 NPs was studied. The determination of cytotoxicity in hFOB 1.19 cells provides a foundational knowledge for an allowable concentration of MgO/Mg(OH) 2 NPs that might be released from biodegradable Mg-based alloys in their application in orthopedic implants in future in vivo studies. The immersion test result showed that MgO/Mg(OH) 2 NPs degraded at a faster rate with the release of increased OH − ions at higher concentrations (50 mM and 100 mM), which was determined by the change in the pH values from days 1 to 7. However, there was no significant difference observed between the change in the pH values of 50-mM and 100-mM concentrations; therefore, we selected 100-mM concentrations of MgO/Mg(OH) 2 to conduct SEM-EDX mapping to understand the element depositions on MgO/Mg(OH) 2 NPs after the immersion test. SEM-EDX mapping showed the presence of Mg, O, Na, Ca, P, Cl, and K in both MgO and Mg(OH) 2 NPs.
Further, an in vitro cytotoxicity study in hFOB 1.19 cells in response to the exposure to various concentrations (1 mM, 5 mM, 10 mM, and 50 mM) of MgO/Mg(OH) 2 NPs (observed by live/dead assay) showed cell proliferation and viability at lower concentrations (5 mM or less). However, at higher concentrations (10 mM and 50 mM) of NPs, an agglomeration of the cells was observed, which indicated the formation of complex compounds that might be the reason for cell death in hFOB 1.19 cells.