• The Journal of Advanced Prosthodontics
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• 제1권1호
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• pp.10-18
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• 2009

STATEMENT OF PROBLEM. Despite an improved bone reactions of Mg-incorporated implants in the animals, little yet has been carried out by the experimental investigations in functional loading conditions. PURPOSE. This study investigated the clinical and histologic parameters of osseointegrated Mg-incorporated implants in early loading conditions. MATERIAL AND METHODS. A total of 36 solid screw implants(diameter 3.75 mm, length 10 mm) were placed in the mandibles of 6 beagle dogs. Test groups included 18 Mg-incorporated implants. Turned titanium implants served as control. Gold crowns were inserted 4 weeks after implant placement and the dogs were immediately put on a food diet. Implants were observed for 10 weeks after loading. Radiographic assessments and stability tests were performed at the time of fixture installation, $2^{nd}$ stage surgery, 4 weeks after loading, and 10 weeks after loading. Histological observations and morphometrical measurements were also performed. RESULTS. Of 36 implants, 33 displayed no discernible mobility, corresponding to successful clinical function. There was no statistically significant difference between test implants and controls in marginal bone levels(P=.46) and RFA values. The mean BIC % in the Mg-implants was $54.5{\pm}8.4%$. The mean BIC % in the turned implant was $45.3{\pm}12.2%$. These differences between the Mg-implant and control implant were statistically significant(P=.005). CONCLUSIONS. The anodized, Mg-incorporated implant demonstrated significantly more bone-to-implant contact(BIC) in early loading conditions. CLINICAL IMPLICATIONS. The results of this study in beagle dogs suggest the possibility of achieving predictable stability of early loaded free-standing dental implants with Mg-incorporated surface.

• Maxillofacial Plastic and Reconstructive Surgery
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• 제32권2호
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• pp.107-111
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• 2010

Purpose: The aim of this study is to compare the stability between Mg-incorporated implant, TiUnite and Machined implant. Materials and Methods: Premolars of 3 Mini pigs (24 months) were extracted. After 2 months later, total 27 fixtures of implants (9 of each design : Machined/ TiUnite/ Mg-incorporated) were inserted into the mandible of 3 mini-pig. Implant stability was estimated by RFA in installation to 2, 4 & 6 weeks. Statistical analysis of RFA values was performed with time and between groups using repeated measure ANOVA and turkey's multiple comparison test. Results: In analyzing the mean value for the observation periods, three types of implants yielded a slight decrease in RFA mean value after 2 week, followed by increase at 4-6 weeks. Mg incorporated oxidized implants demonstrated significantly higher RFA mean values at 6 weeks comparing other groups. The difference of RFA value with time and between groups was statistically significant. Conclusion: We concluded that Mg implants may reduce failure rates of clinical implants In the early period of bone healing and Mg implants may shorten the bone healing time from surgery to functional loading.

• 구강회복응용과학지
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• 제24권4호
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• pp.337-349
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• 2008

최적의 골유착을 얻기 위하여 임플란트 디자인의 개선과 다양한 표면처리 방법이 개발되어 왔는데, 특히 최근 알칼리 에칭과 이온 주입법, 양극산화법 등 생화학적인 골유착을 유도할 수 있는 표면개질 방법이 관심의 대상이 되고 있다. 이러한 방법 중 마그네슘 이온을 함유한 전해액속에서 양극산화피막처리한 임플란트(마그네슘 임플란트)를 이용하여 조기 하중의 가능성이 제시된 바 있다. 그러나 마그네슘 임플란트의 경우 장기간의 기능적 하중을 가한 경우에 대한 연구가 부족한 상태이므로, 이에 본 연구에서는 비글견을 이용한 동물실험을 통해 지연하중을 가한 마그네슘 임플란트의 방사선적, 임상 안정성 검사 및 조직형태학적 분석을 시행하여 화학적 표면개질 임플란트의 골조직 반응을 기계가공 임플란트와 비교 평가하고자 하였다. 발치 후 3개월의 치유과정을 가진 비글 성견 6마리의 하악에 좌우 3개씩 실험용으로 제작된 직경 3.75 mm, 길이 10.0 mm의 나사 형태 임플란트 36개를 보편적인 임플란트 시술시 이용하는 식립법을 이용하여 식립하였다. 18개의 대조군은 기계가공만 한 상태였고, 실험군은 마그네슘을 함유한 전해액에서 양극산화 피막처리하였다. 식립 후 3개월 동안의 치유기간 후 이차수술을 실시하였으며, 연결고정하지 않고 단일치 금관수복으로 보철물을 장착하여 하중을 가하였다. 3개월 동안 하중을 가한 후에 희생시켜 비탈회 연마 표본을 제작하여 조직형태 계측학적 분석을 시행하였다. 임플란트 식립시, 이차 수술시, 하중을 가한 1개월, 3개월 후에 변연골 흡수를 평가하기 위해 방사선학적 검사를 실시하였고, 골계면 사이에서의 안정성을 평가하기 위해 공진주파수 수치를 측정하였다. Mann-Whitney U test와 repeated measured ANOVA를 이용하여 95 퍼센트 유의수준으로 통계적 유의성을 확인하였다. 총 36개의 임플란트 중 8개에서 일차 수술 후 골유착의 실패가 나타났으며, 1개는 3개월의 부하 후에 실패 양상이 나타났다. 공진주파수분석결과, 마그네슘 임플란트군은 대조군과는 달리 공진주파수 수치가 증가하다가 다소 감소하는 양상을 보였으며, 하중을 가한 3개월 후에는 두 군의 수치가 비슷하였다. 방사선 사진 분석 결과 두 군 모두 시간에 따른 변연골 흡수량이 증가하였으며, 통계적으로 유의한 차이는 없었다. 조직형태학적인 분석 결과 마그네슘-임플란트가 대조군에 비해 더 높은 수치의 골임플란트 계면접촉율을 보여 주었으나, 나사산내 골면적은 더 낮았다. 그러나 두 군 모두에서 통계적 유의성은 없었다. 이상의 결과에서 지연 하중을 가하는 경우에 있어서 골유착에 대한 마그네슘-임플란트의 효과는 기계가공된 임플란트와 유사하였다. 조기 하중시 더 빠르고 강한 골반응을 보여주던 이전 연구와 종합하여 볼 때, 마그네슘 임플란트는 즉시 또는 조기 하중 가능성을 증진시켜 주며, 지연 하중에서는 생체 적합성이 우수한 타이타늄과 유사한 골유착 정도를 보이는 것으로 사료된다. 그러나 임상적으로 화학적 표면개질 방법의 유용성을 판단하기 위해 다양하고 장기적인 임상 연구가 필요하리라 사료된다.

• 대한치과보철학회지
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• 제50권3호
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• pp.176-183
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• 2012

연구 목적: 부분 무치악 환자에서 Mg titanate implant (M Implant system, Shinhung, Korea)의보철 후 1년간의 방사선사진을 이용한 변연골 흡수량과 Osstell$^{(R)}$을 이용한 임플란트 안정성 평가 결과를 분석하여 임상적인 성공률에 대해 알아보고자 한다. 연구 재료 및 방법: 38명의 환자에 79개의 임플란트를 식립하여 보철 후 1년 동안 변연골 흡수량, 임플란트의 동요도, 임플란트 식립 위치에 따른 분포 및 성공률, 보철 전후에 따른 성공률을 분석했다. 결과: 변연골의 흡수량은 보철물 장착 후 1년간의 평가에서 상악에서는 평균 1.537 mm, 하악에서는 평균 1.172 mm의 변연골 흡수가 관찰되었으며, 전체적인 상하악의 평균 변연골 흡수량은 1.255 mm로 관찰되었다. 수술 후 시간이 경과함에 따라 ISQ값은 미약하게 감소하였다가 증가하는 경향을 보였으나, 상악과 하악 모두에서 식립 당일 이후 예비 인상일, 최종 보철물의 장착일과 주기적인 평가 기간 동안 ISQ값의 큰 증가나 감소를 나타내지는 않았다. 성공률은 상악에서의 94.12%였고, 하악에서의 98.39%였다. 결론: 본 실험의 결과로 미루어 Mg titanate implant는 임상적으로 양호한 결과를 보여주었다.

• 구강회복응용과학지
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• 제27권1호
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• pp.25-39
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• 2011

마그네슘 양극산화 임플란트는 동물실험에서 우수한 골반응을 나타내었지만 이에 대한 임상 연구는 전무하다. 본 연구에서는 마그네슘 양극산화 임플란트의 단기간 성공률 및 안정성, 변연골 흡수량을 평가하고자 하였다. 강릉원주대학교 치과병원의 임상시험위원회의 승인을 거쳐 건강한 부분 무치악 환자에게 마그네슘 양극산화 임플란트를 식립한 후 일반적인 프로토콜에 따라 보철 치료를 시행하였다. 1차 수술, 2차 수술, 보철물 시적, 하중 후 1개월, 3개월, 6개월 평가를 시행하였으며, 매회 내원 시 임플란트 안정지수(Implant stability quotient, ISQ)를 측정하고 구내 치근단 방사선 사진에서 변연골 흡수량을 산출하였다. 반복측정이 있는 분산분석법을 이용하여 통계적 분석을 시행하였다. 총 50명에게 식립된 101개의 임플란트 중 골유착에 실패한 임플란트는 없었으며, 하중 후 6개월 성공률은 100%였다. 평균 ISQ는 시간이 경과함에 따라 증가하였으며 여성보다 남성에서, 상악보다 하악에서 높게 나타났다 (P<.05). 하중 6개월 후 골질이 양호할수록, 고정체 직경이 클수록 높은 ISQ 값을 보였다 (P<.05). 하중 후 6개월간 평균 변연골 흡수량은 0.26 mm로 관찰되었으며 하악보다 상악에서, 여성보다 남성에서 더 많은 흡수가 관찰되었다. 본 연구의 마그네슘 양극산화 임플란트의 6개월 성공률은 100%이며, 낮은 골질에서도 우수한 골유착이 관찰되었다. 안정성과 변연골 수준 또한 만족스러운 결과를 보였지만 더욱 장기적인 임상연구가 필요하다고 사료된다.

• Journal of Periodontal and Implant Science
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• 제33권1호
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• pp.1-11
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• 2003

Hydroxyapatite(HA) has been extensively used as bone graft materials and tooth implant surface coating materials because of its biocompatibility and osteoconductive properties. However, as HA is intrinsically poor in mechanical properties, zirconia($ZrO_2$) was incorporated with HA as reinforcing phases for improvement of mechanical properties. The purpose of this study was to investigate the biological activities of HA-coated zirconia through the cell proliferation test, measurements of alkaline phosphatase activity, and histologic examination. Four kinds of tested blocks were prepared according to the pore size (300-500${\mu}m$/500-700${\mu}m$) and the porosity (70%/90%). Cell proliferation and alkaline phosphatase activity was measured at 1, 7, 14 days. The number of cells proliferate after 7, 14 days were significantly increased in all groups when compared with that of the first day, but there was no significant difference between the 4 groups at each time period. At the 7 day, alkaline phosphatase activities of cells cultured in 4 groups were higher than that of the first day, but there was no significant difference between the 4 groups at each time period. The human gingival fibroblast and MG 63 cell was used to evaluate the cell cytotoxicity using MTT test. The materials tested in the current study turned out to be non-cytotoxic. In histologic examination(SEM), at 1 day there were many cells attached on the surfaces of all kinds of tested blocks. The number of cells were increased over time. At the 14 day, there were more cells proliferated than 1 day and some of the pores of blocks were partially filled with the proliferated cells. The in vitro response of osteoblast-like cells to the HA-coated zirconia showed comparable effect on transformation comparable to hydroxyapatite.

• Journal of Periodontal and Implant Science
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• 제35권4호
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• pp.939-948
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• 2005

The role of the periosteum on osteointegration of $Bio-Oss^{(R)}$(Geistlich, Wolhusen/Switzerland) was studied in rabbit calvarial defect. 12 New Zealand white male rabbits between 2.8 and 4 kg were included in this randomized, blinded, prospective study. Each rabbit was anesthetized with Ketamine HCl(5 mg/kg) and Xylazine HCl(1.5 ml/kg). An incision was made to the bony cranium and the periosteum was reflected. Using a 6-mm trephine bur(3i. USA), four 8-mm defects were created with copious irrigation. The defects were classified into barrier membrane($Tefgen^{(R)}$, Lifecore Biomedical. Inc, U.S.A.) only group as a control, $Bio-Oss^{(R)}$ with barrier membrane group, $Bio-Oss^{(R)}$ with periosteum covering group, and $Bio-Oss^{(R)}$ without periosteum covering group. There were 2 rabbits in each group. The wound was closed with resorbable suture materials. Rabbits were sacrificed using phentobarbital(100 mg/kg) intravenously at 1, 2, and 4 weeks after surgery. The samples were fixed in 4% paraformaldehyde, and decalcified in hydrochloric acid decalcifying solution(Fisher Scientific, Tustin, CA) at $4^{\circ}C$ for 2-4 weeks. It was embedded in paraffin and cut into 6 ${\mu}m$ thickness. The sections were stained with H & E and observed by optical microscope. The results were as follows; 1. The periosteum played an important role in osteointegration of $Bio-Oss^{(R)}$ in bone defects. 2. When the periosteum remained intact and $Bio-Oss^{(R)}$ was placed on the defect, $Bio-Oss^{(R)}$ with periosteum covering has been incorporated into the newly formed bone from 2-week postoperatively. 3. When the periosteum was removed at the surgical procedure, invasion of connective tissue took place among the granules, and new bone formation was delayed compared to periosteum covering group. Therefore, when the bone grafting was performed with periosteal incision procedure to achieve tension-free suture, the integrity of the overlying periosteum should be maintained to avoid fibrous tissue ingrowth.

• Journal of Periodontal and Implant Science
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• 제26권2호
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• pp.469-490
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• 1996

The initial events required for periodontal regeneration is the attachment, spreading, and proliferation of appropriated cells at the healing sites. These have been reported that minocycline stimulates the attachment of periodontal ligament cells, and also $TGF-{\beta}1$ enhances the proliferation of periodontal ligament cells. The purpose of the present study was to evaluate the effects of $TGF-{\beta}1$ on the cellular activity of minocycline treated human periodontal ligament cells. Periodontal ligament cells were obtained from the explants of healthy periodontal ligaments of extracted 3rd molars or premolar teeth extracted from the patients for orthodontic treatment. The cells were cultured in minimal essential medium(${\alpha}-MEM$) supplemented with 10.000units/ml penicillin, $10,000{\mu}g/ml$ streptomycin and 10% FBS(fetal bovine serum) at $37^{\circ}C$ in a humidified atmosphere of 5% carbon dioxide and the 5th to the 8th passages of the cells were used. To evaluate the effect of minocycline on cell attachment, the cells were seeded at a cell density of $1.5{\times}10^4$ cells/well in 24-well culture plates and treated with $20{\mu}g/ml$ and $100{\mu}g/ml$ of minocycline for 1.5 h. After trypsinization, the cells were counted with hemocytometer and were taken photographs for observation of cellular morphology. To evaluate the effect of $TGF-{\beta}1$ on minocycline-pretreated periodontal ligament cells, the cells were seeded at a cell density of $1{\times}10^4$ cells/ well in 24-well culture plates and treated with $20{\mu}g/ml$ and $100{\mu}g/ml$ of minocycline for 1.5 h. After incubation, 1 and 10ng/ml of $rh-TGF-{\beta}1$ were also added to the each well and incubated for 1 and 2 days, respectively. Then, MTT assay, DNA synthesis($^3H-thymidine\;assay$), and protein and collagen assay(3H-proline assay) were carried out. In the MIT assay, after 200ul MTT solutionlconeentration of 5mg/ml) were added to the each well of the 24-well plates and incubated for 3 hours, and 200 ul DMSO were added so as to dissolve insoluble blue formazan crystals which was formed in incubated period. Then it read plates on a ELISA reader. For mitogenic assay, 1 uCi/ml $^3H-thymidine$ was added to each well for the final 2 hours of the incubation periods. After labeling, the wells were washed 3 times with ice cold PBS and 4 times with 5% TCA to remove unincorporated label and precipitate the cellular DNA. DNA, with the incorporated $^3H-thymidine$, was solubilized with 500 ul of 0.1% NaOH/0.1% SDS. A 250 ul aliquot was removed from each well and placed in a scintillation vial with 4ml of scintillation cocktail. Using an liguid scintillation counter, counts per minute(CPM) were determined for each samples. 3 uCi/ml $^3H-proline$ was added to each well for the final 4 hours of the incubation periods and total protein and percent collagen synthesis were carried out. The results indicate that minocycline treated group with $100{\mu}g/ml$ concentration for 1.5 hours significantly increased than that of control in cell attachment, and cell process is also evident compared with that of control in cell morphology, and the cellular activity and DNA synthesis rate of cells treated minocycline and $TGF-{\beta}1$ significantly increased than that of control values, but were below to values of the $TGF-{\beta}1$ only treated group in MIT assay and $^3H-thymidine\;assay$, and the total protein synthesis of minocycline and $TGF-{\beta}1$ treated group also significantly increased than that of control values, but the percent collagen synthesis of tested group significantly decreased to compared with control. On the above the findings, the tested group of minocycline and $TGF-{\beta}1$ did not increase the effect on the cell activity than $TGF-{\beta}1$ only tested group and the tested group of minocycline inhibited cell activity. This results indicate that minocycline was effective on cell attachment in early stage, but it is harmful to cell activity, that inhibitory effect of minocycline was compensated with stimulatory effect of $TGF-{\beta}1$.