Abstract:Bone-forming cells and Mϕ play key roles in bone tissue repair. In this study, we prepared a superhydrophilic titanium implant functionalized by ozone gas to modulate osteoconductivity and inhibit inflammatory response towards titanium implants. After 24 h of ozone gas treatment, the water contact angle of the titanium surface became zero. XPS analysis revealed that hydroxyl groups were greatly increased, but carbon contaminants were largely decreased 24 h after ozone gas functionalization. Also, ozone gas fun… Show more
“…The surface topography/roughness, hydrophilicity, and chemical composition potentiate cellular responses to materials [6,7,9,[36][37][38][39]. However, in the present study, all of the functionalized surfaces showed similar surface topography/roughness to those of bare PEEK, and thus can be excluded as a factor in the observed differences of MSCs behaviors on the functionalized PEEK.…”
Section: Discussioncontrasting
confidence: 49%
“…Alternatively, PEEK has a highly hydrophobic surface, but surfaces became more hydrophilic after surface functionalization. It is widely accepted that a hydrophilic surface produced a more pronounced effect on the cell responses than a hydrophobic surface [36][37][38][39]. Notably, the O 3 -Ca and O 3 -PCa showed enhanced cell proliferation compared with the bare at three and seven days.…”
Section: Discussionmentioning
confidence: 94%
“…Rat MSCs were isolated from femurs of specific-pathogen-free (SPF) Wistar rats (male, four weeks old; Japan SLC, Shizuoka, Japan) and were cultured in Minimum Essential Medium α (MEMα) supplemented with 15% heat-inactivated fetal bovine serum (FBS), 100 U/mL penicillin, 100 µg/mL streptomycin, and 0.25 µg/mL amphotericin B (all from Thermo Fisher Scientific) as previously described [36].…”
Biomedical applications of poly(ether ether ketone) (PEEK) are hindered by its inherent bioinertness and lack of osseointegration capability. In the present study, to enhance osteogenic activity and, hence, the osseointegration capability of PEEK, we proposed a strategy of combined phosphate and calcium surface-functionalization, in which ozone-gas treatment and wet chemistry were used for introduction of hydroxyl groups and modification of phosphate and/or calcium, respectively. Surface functionalization significantly elevated the surface hydrophilicity without changing the surface roughness or topography. The cell study demonstrated that immobilization of phosphate or calcium increased the osteogenesis of rat mesenchymal stem cells compared with bare PEEK, including cell proliferation, alkaline phosphatase activity, and bone-like nodule formation. Interestingly, further enhancement was observed for samples co-immobilized with phosphate and calcium. Furthermore, in the animal study, phosphate and calcium co-functionalized PEEK demonstrated significantly enhanced osseointegration, as revealed by a greater direct bone-to-implant contact ratio and bond strength between the bone and implant than unfunctionalized and phosphate-functionalized PEEK, which paves the way for the orthopedic and dental application of PEEK.
“…The surface topography/roughness, hydrophilicity, and chemical composition potentiate cellular responses to materials [6,7,9,[36][37][38][39]. However, in the present study, all of the functionalized surfaces showed similar surface topography/roughness to those of bare PEEK, and thus can be excluded as a factor in the observed differences of MSCs behaviors on the functionalized PEEK.…”
Section: Discussioncontrasting
confidence: 49%
“…Alternatively, PEEK has a highly hydrophobic surface, but surfaces became more hydrophilic after surface functionalization. It is widely accepted that a hydrophilic surface produced a more pronounced effect on the cell responses than a hydrophobic surface [36][37][38][39]. Notably, the O 3 -Ca and O 3 -PCa showed enhanced cell proliferation compared with the bare at three and seven days.…”
Section: Discussionmentioning
confidence: 94%
“…Rat MSCs were isolated from femurs of specific-pathogen-free (SPF) Wistar rats (male, four weeks old; Japan SLC, Shizuoka, Japan) and were cultured in Minimum Essential Medium α (MEMα) supplemented with 15% heat-inactivated fetal bovine serum (FBS), 100 U/mL penicillin, 100 µg/mL streptomycin, and 0.25 µg/mL amphotericin B (all from Thermo Fisher Scientific) as previously described [36].…”
Biomedical applications of poly(ether ether ketone) (PEEK) are hindered by its inherent bioinertness and lack of osseointegration capability. In the present study, to enhance osteogenic activity and, hence, the osseointegration capability of PEEK, we proposed a strategy of combined phosphate and calcium surface-functionalization, in which ozone-gas treatment and wet chemistry were used for introduction of hydroxyl groups and modification of phosphate and/or calcium, respectively. Surface functionalization significantly elevated the surface hydrophilicity without changing the surface roughness or topography. The cell study demonstrated that immobilization of phosphate or calcium increased the osteogenesis of rat mesenchymal stem cells compared with bare PEEK, including cell proliferation, alkaline phosphatase activity, and bone-like nodule formation. Interestingly, further enhancement was observed for samples co-immobilized with phosphate and calcium. Furthermore, in the animal study, phosphate and calcium co-functionalized PEEK demonstrated significantly enhanced osseointegration, as revealed by a greater direct bone-to-implant contact ratio and bond strength between the bone and implant than unfunctionalized and phosphate-functionalized PEEK, which paves the way for the orthopedic and dental application of PEEK.
“…On hydrophilic implant surfaces, molecules are adsorbed in a more flexible pattern, leading to an enhanced interaction between the implant surface and the surrounding environment. Previous studies reported that hydrophilic surfaces demonstrated anti-inflammatory property by mitigating the pro-inflammatory cytokines production and inflammatory response of macrophages 23 24 . Since surface chemistry influences surface wettability 22 , the surface chemistry may be the most critical factor in modulating DC response.…”
Dendritic cells (DCs) play a pivotal role in the host response to implanted biomaterials. Osseointegration of titanium (Ti) implant is an immunological and inflammatory-driven process. However, the role of DCs in this complex process is largely unknown. This study aimed to investigate the effect of different Ti surfaces on DC maturation, and evaluate its subsequent potential on osteogenic differentiation of preosteoblasts. Murine bone marrow-derived DCs were seeded on Ti disks with different surface treatments, including pretreatment (PT), sandblasted/acid-etched (SLA) and modified SLA (modSLA) surface. Compared with DCs cultured on PT and SLA surfaces, the cells seeded on modSLA surface demonstrated a more round morphology with lower expression of CD86 and MHC-II, the DC maturation markers. Those cells also secreted high levels of anti-inflammatory cytokine IL-10 and TGF-β. Notably, addition of conditioned medium (CM) from modSLA-induced DCs significantly increased the mRNA expression of Runx2 and ALP as well as ALP activity by murine preosteoblast MC3T3-E1 cells. Our data demonstrated that Ti disks with different surfaces lead to differential DCs responses. PT and SLA surfaces induce DCs mature, while DCs seeded on modSLA-Ti surface maintain an immature phenotype and exhibit a potential of promoting osteogenic differentiation of MC3T3-E1 cells.
“…Preparing a superhydrophilic titanium implant functionalised with ozone gas can modulate osteoconductivity and inhibit the inflammatory response to titanium implants. This superhydrophilic surface has been proposed to be useful as an endorsed implantable biomaterial and as a biomaterial for implantation in other tissues (13). The effect of ozone treatment in combination with autogenous bone grafts on bone healing in rat calvaria has been investigated.…”
Background:The present study presents the evaluation of the damage in the bone tissue resulting from a calvarial defect in rats and the efficiency of exposure to an ozone application with an alloplastic bone graft on the calvarial bone damage.
Materials and methods:Wistar male rats (n = 56) were divided into four groups: a control group (n = 14), defect and ozone group (n = 14), defect and graft group (n = 14), and defect, graft, and ozone group (n = 14). Under anaesthesia, a circular full-thickness bone defect was created in all groups, and the experimental groups were further divided into two sub-groups, with seven rats in each group sacrificed at the end of the 4 th and 8 th weeks. Bone samples were dissected, fixed in 10% formalin solution, and decalcified with 5% ethylene-diaminetetraacetic acid (EDTA). After the routine follow-up on tissues, immunostaining of osteopontin and osteonectin antibodies was applied to sections and observed under a light microscope.
Results:The control group exhibited osteopontin and osteonectin expression in fibroblasts and inflammatory cells at the end of the 4 th week with an acceleration at the 8 th week. Ozone administration elucidated new trabecular bone formation by increasing osteoblastic activity.Lastly, our observations underscore that a combination of allograft and ozone application increased the osteoblast, osteocyte, and bone matrix development at the 4 th and 8 th weeks.
Conclusions:Exposure to an ozone application with an alloplastic bone graft on calvarial bone damage may induce osteoblastic activity, matrix development, mature bone cell formation, and new bone formation in rats.
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