- Nano Express
- Open Access
Endothelialization of TiO2 Nanorods Coated with Ultrathin Amorphous Carbon Films
© Chen et al. 2016
- Received: 30 January 2016
- Accepted: 7 March 2016
- Published: 15 March 2016
Carbon plasma nanocoatings with controlled fraction of sp3-C bonding were deposited on TiO2 nanorod arrays (TNAs) by DC magnetic-filtered cathodic vacuum arc deposition (FCVAD). The cytocompatibility of TNA/carbon nanocomposites was systematically investigated. Human umbilical vein endothelial cells (HUVECs) were cultured on the nanocomposites for 4, 24, and 72 h in vitro. It was found that plasma-treated TNAs exhibited excellent cell viability as compared to the untreated. Importantly, our results show that cellular responses positively correlate with the sp3-C content. The cells cultured on high sp3-C-contented substrates exhibit better attachment, shape configuration, and proliferation. These findings indicate that the nanocomposites with high sp3-C content possessed superior cytocompatibility. Notably, the nanocomposites drastically reduced platelet adhesion and activation in our previous studies. Taken together, these findings suggest the TNA/carbon scaffold may serve as a guide for the design of multi-functionality devices that promotes endothelialization and improves hemocompatibility.
- TiO2 nanorods
- Amorphous carbon coatings
- Human umbilical vein endothelial cells
Anti-thrombogenicity and endothelialization are two essential issues in devising blood-contacting medical implants, such as artificial blood vessels and vascular stents [1, 2]. Minimizing the plasma protein adsorption and platelet adhesion has proved beneficial in reducing thrombus formation especially in the initial implantation. Subsequently, rapid endothelialization of implant surfaces may significantly reduce the risk of long-term thrombogenesis and provide a fully hemocompatible interface. Furthermore, native endothelium has unique physiological role of maintaining vascular homeostasis, including the active anti-thrombosis, and the release of soluble factors that contribute to the inhibition of smooth muscle cell proliferation and hence reduce intimal hyperplasia [3, 4]. Rapid regeneration of endothelium is thereby crucial to the success of implantation. Numerous approaches such as natural polymer coating (collagen) , surface biomolecule immobilization (heparin) , and drug-eluting coatings (paclitaxel)  have been demonstrated to be able to decrease the risk of thrombosis, but the instability, temporality, and the side effect limit their clinical use.
The nano- and microstructure of surfaces with physical attributes has been established as a decisive factor affecting biological responses. Sub-micrometer textures , poly(carbonate urethane)-coated carbon nanotube , TiO2 nanotube layers , and lotus-leaf-like structured polymer film , have been reported to remarkably decrease the activation and adhesion of platelets. However, these surfaces exhibited superhydrophobicity (CA > 150°) or approximately superhydrophobicity and focus on hindering only the adhesion of platelets to surfaces. In most cases, cell function was found be suppressed on the highly hydrophobic materials [12, 13]. Hence, ideal blood-contact biomaterials should maintain good anti-thrombogenicity and has positive effects on cell behavior. Recently, Ding et al. suggest that the anisotropic pattern featuring 1-μm grooves could enhance endothelialization and reduce platelet adhesion and activation .
Amorphous and crystalline carbon films deposited on metals have been studied as possible candidates for biomedical applications, mainly because of their chemical inertness, lack of cytotoxicity, and the natural presence of this element in the human body [15, 16]. The TiO2 nanorod arrays (TNAs) showed outstanding blood compatibility due to its special surface topography and hydrophobicity in our previous work . After being coated with a-C films, the hemocompatibility of TNA nanocomposites was better than that of the separate TNA or a-C films [18, 19]. In this work, we reported the in vitro bioactivity and cytocompatibility of human umbilical vein endothelial cells (HUVECs) on the TNA/carbon films with different sp3-C bonding but independent of surface topography. Our data clearly demonstrate that amorphous carbon films significantly improve cell viability and suggest the possibility that sp3-C containing in carbon films must have been one of the important factors contributing to the wettability and cell cytocompatibility of TNA/carbon nanocomposites.
Synthesis of TNA/ta-C Composites
The single crystal rutile TNAs was synthesized on a piece of fluorine-doped tin oxide (FTO) glass substrates by the solvent-thermal method. 22.5-mL deionized water was mixed with 17.5-mL hydrochloric acid (36.5–38 % by weight) to reach a total volume of 40 mL in a Teflon-lined stainless steel autoclave (100 mL). The mixture was stirred for 5 min before the addition of 0.4 ml tetrabutyl titanate (99 % J&K Scientific). After stirring for another 5 min, four pieces of FTO substrates (3.0 × 0.5 × 0.2 cm3), separately cleaned with sonication in acetone, ethanol, and deionized water each for 15 min, were leaned against the wall of the Teflon-liner with the conductive side facing down. The solvent-thermal synthesis was conducted at 140 °C for 6 h. After the synthesis, the autoclave was cooled to room temperature and the FTO substrate was taken out, rinsed with deionized water, and dried in nitrogen stream. Subsequently, the oriented TNAs grown on FTO substrates were subjected to pure C+ ion flux produced by the FCVAD system. C+ plasma was generated by igniting an electric arc between a mechanical trigger and a graphite cathode (99.99 %) with a continuous DC current of 50 A. An ultrathin (10 nm) ta-C film was deposited on the top of TNAs by applying a negative bias voltage to the FTO substrate. The ratio of sp3 to sp2 bonds of the ta-C film was adjusted by the energy of carbon ions. In this work, three kinds of substrate bias voltage were applied to accelerate the carbon ions. As a result, the carbon thin films C1, C2, and C3 are provided with higher, medium, and lower sp3-C content, respectively.
The structure of TNAs grown on FTO substrate was characterized by the X-ray diffractometer (XRD, BrukerD8 Discover) with a Cu-Kα 1 radiation (k = 1.54 Å) at the scanning speed of 2°/min. The topography of TNAs was observed by field emission scanning electron microscope (SEM, FEI Quanta-400, Holland). The electronic structure of ta-C films was examined by an X-ray photoelectron spectroscopy (XPS, ESCALAB 250, Thermo-VG Scientific). A monochromic Al-Kα source with a spot size of 500 μm and pass energy of 20 eV was used for this measurement. Sample cleaning was not performed before the XPS analysis in order to preserve the elemental and physicochemical state of the sample surface.
Static contact angle measurements were performed by a video contact angle goniometer (SL2008 Powereach, China) based on the sessile drop method. The mean value was calculated from five individual measurements.
Prior to cell culture, the FTO substrates with TNAs were cut into pieces (1.0 × 1.0 cm2) and were wrapped by sterilization pack and sterilized by autoclave. After being dried at 60 °C for 24 h, the samples then transferred in individual wells of 24-well culture plates. The HUVECs (ATCC CRL-1730) were cultured in endothelial cell medium (ECM, ScienCell) supplemented with 5 % fetal bovine serum, 1 % endothelial cell growth supplements (ECGS), and 1 % penicillin–streptomycin. Incubation was carried out at 37 °C in an atmosphere of 5 % CO2. After 80 % confluence, HUVECs were suspended in complete medium and seeded onto the various substrates at a concentration of 5 × 104 cells per well.
After 24 h of culture, the cell viability of HUVECs adhered on different TNA substrates were assessed using a cell-permeable dye calcein-AM (Invitrogen) and a cell-impermeable DNA-binding dye propidium iodide (PI, Sigma-Aldrich). The cells were incubated in phosphate-buffered saline (PBS) containing 5 μg/mL calcein-AM and 50 μg/mL PI at 37 °C for 20 min and then immediately examined under a fluorescence microscope (Leica DM2500). At least eight random regions on each sample were chosen to be photographed, and the mean number of live cells was calculated.
Cell Attachment and Proliferation
Cell attachment was evaluated by counting the cell numbers on substrates after 4-h incubation. Cell proliferation was determined by measuring the increase in cell numbers from 24 to 72 h of culture without renewal of the medium. At defined time points, the HUVECs cultured on experimental substrates were fixed with 4 % paraformaldehyde in PBS for 20 min at room temperature. Fixed cells were then permeabilized with 1 % Triton X-100 (Sigma-Aldrich) in PBS for 5 min and blocked with 1 % bovine serum albumin (BSA; Sigma-Aldrich) in PBS for 60 min. To examine the cytoskeleton, the F-actin of the fixed cells was incubated with 2 μg/mL phalloidin tetramethyl rhodamine isothiocyanate (TRITC; Sigma-Aldrich) for 60 min. The cells were also counterstained with Hoechst solution (Sigma-Aldrich) to image the nucleus. To determine the cell attachment and proliferation, the mean cell number of each substrate was analyzed from at least 10 fields at ×40 magnifications. Hoechst-stained nucleus was counted by using the “Analyze particles” tool in ImageJ software.
To ensure reproducibility and obtain better statistics, all assays were repeated in triplicate. All data are expressed as means value ± standard error (SE). The data were subjected to one-way ANOVA to determine the statistical difference. In all cases, a p value of <0.05 was considered statistically significant.
Relative fraction of sp2, sp3, and C–O components for ta-C films deposited at different biases
C1 (−100 V)
C2 (−300 V)
C3 (−900 V)
In our experiment, ~15,000–20,000 TiO2 nanorods were exposed to each cell. Thus, we raised the possibility that a large number of TNAs were engulfed by cells. If that is the case, the long-term toxicity caused by TNA engulfment may lead to the cell death. Indeed, the TiO2-based nanomaterials (including nanotubes, nanowires, and nanoparticles) have been widely reported to be cytotoxic in mammalian cells, inducing cell death by apoptosis and necrosis . The results of Lee et al. suggested that ZnO nanorods with diameter similar to ours are engulfed by umbilical vein endothelial cells also lead the cells death . But they considered that the cell adhesion and survival has no obvious relationship with the surface chemistry of ZnO nanorods (with or without silicon dioxide coating) . However, the surface chemical properties play an important role in our work. The a-C film-coated TNAs exhibited superior cell viability compare to the pure TNAs. We considered it was mainly attributed to the ultrathin carbon coating, which acted as a barrier preventing the delivery of toxic material into cells.
These phenomena could be attributed to the changes in surface wettability and chemical composition after carbon plasma coating. Surface wettability is believed to be an important factor that guides the first events occurring at the cell/biomaterial interface, such as interaction of medium and proteins with biomaterial and subsequent cell responses . The superhydrophobic TNA substrate not only results in poor cell attachment in the initial seeding (Figs. 7 and 8) but also cause the further inhibition of cell proliferation and cell clustering because the weak cell-surface interaction . In addition, we cannot rule out the possibility that long-term toxicity of TiO2 nanorods due to engulfment, which would decrease cell survival and suppress cell proliferation subsequently at the long times. More detailed studies are needed to investigate this possibility.
On the other hand, the TNAs after carbon plasma treating exhibited a superior proliferative capacity. Our data suggested that the ta-C films play an important role in regulating cell proliferation, which not only shielded the HUVECs from toxicity but also regulated the wettability by electronic structure (sp2/sp3 rate). The a-C film-coated TNAs with the highest sp3-C content result in lowest water CA (101.8°) and present the best cell attachment and proliferation, whereas the pure TNAs (CA = 144.8°) do the opposite thing. Our results are consistent with the work of Ranella et al. . They suggested that cell response shows a non-monotonous and sigmoidal dependence on the synergy of surface roughness and chemistry, which determines the wettability or surface energy of the culture substrate (3D micro/nanosilicon surfaces). They revealed that optimal cell adhesion and spreading was obtained on the substrate of small roughness and moderate wettability (CA = 105°). On the contrary, they founded cell response was effectively inhibited on highly rough and superhydrophobic substrates (CA = 152°).
In this work, the ta-C films with controlled fraction of sp3-C were deposited on TNAs without changing the surface topography of substrates. The wettability of substrates was determined by sp3 to sp2 ratio, and the sp3-C-rich surfaces present more hydrophilic than sp2C-rich surfaces. The adhesion, viability, proliferation, and morphology of HUVEC cells cultured on TNAs and TNAs/ta-C have been investigated. It was found that the carbon nanocoatings significantly improved cell viability. In addition, the cells were likely to attach on high sp3-C-contented surfaces and exhibit better shape configuration and proliferation. Our data indicate that ta-C film-coated TNAs possess superior cytocompatibility. The excellent cell compatibility is mainly ascribed to the nontoxic properties and moderate wettability of ta-C films adjusted by sp3 to sp2 ratio.
This work was supported by The National Basic Research Program of China (No. 2014CB931700) and the National Natural Science Foundation of China (Nos. 81471787, 61471401, and 81400619).
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