• 한국재료학회지
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• 제22권6호
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• pp.285-291
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• 2012

Hydroxyapatite (HA) is well known as a biocompatible and bioactive material. HA has been practically applied as bone graft materials in a range of medical and dental fields. In this study, two types of dense hydroxyapatite ceramics were prepared from natural bones and synthetic materials. The biocompatibility of HA ceramics for supporting osteoblast cell growth and cytotoxicity using an in vitro MG-63 cell line model were respectively evaluated. Artificial hydroxyapatite shows relative density of 93% with 1-2 ${\mu}m$ after sintering, but a hydroxyapatite compact derived from bovine bone has low sintered density of 85% with a small content of MgO. Irrespective of the starting raw materials, both types of sintered hydroxyapatite displayed similar biocompatibility in the tests. FE-SEM observations showed that most MG-63 cells had a stellar shape and formed an intercellular matrix containing fibers on sintered HA. The cells were well attached and grown over the HA surface, indicating that there was no toxicity.

• 치과방사선
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• 제27권1호
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• pp.87-97
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• 1997

The purpose of this study was to evaluate the method for quantitative assessment of bone mass from aluminum-equivalent value of hydroxyapatite by using digital imaging system consisted of Power Macintosh 7200/120, 15-inch color monitor, and GT-9000 scanner with transparency unit. After aluminum-equivalent image made from correlation between aluminum thickness and grey scale, the accuracy of conversion to mass from aluminum-equivalent value was evaluated. Measured bone mass was compared with converted bone mass from aluminum-equivalent value of hydroxyapatite block by correlation formula between aluminum-equivalent value of hydroxyapatite block and hydroxyapatite mass. The results of this study were as follow; 1. Correlation between aluminum thickness and grey level for obtaining aluminum-equivalent image was high positively associated(r²=0.99). Converted masses from aluminum-equivalent value were very similar to measured masses. There was, statistically, no significant difference(P<0.05) between them 2. Correlation between hydroxyapatite aluminum-equivalent and hydroxyapatite mass was shown to linear relation (r²=0.95). 3. Converted masses from aluminum-equivalent value of 3 dry mandible segments were similar to measured masses. The difference between the exposure directions was not significantly different(P<0.05).

• 한국응용과학기술학회지
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• 제35권2호
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• pp.350-356
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• 2018

수산화인회석은 생체적합성이 뛰어나기 때문에 생체재료로 사용되고 있다. 본 연구에서는 온도, 농도, pH를 조절하여 인산수소칼슘 중간체의 가수분해반응을 통해 c면이 배향된 수산화인회석을 합성하였다. 염기조건에서 전구체의 농도가 낮을 경우 막대 형태의 수산화인회석 결정이 모여 불규칙한 형태의 입자를 만들었고 농도가 높을 경우 수산화인회석결정의 c면이 노출된 판 형태의 입자를 만들었으며 이에 따라 입자의 제타전위 차가 3 mV가 되었다. 생성물의 물리화학적 특성은 XRD, SEM, FT-IR, 제타전위측정기를 통해 평가하였다.

• Korean Chemical Engineering Research
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• 제45권5호
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• pp.473-478
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• 2007

공침법을 이용하여 질산은($AgNO_3$)을 수산화아파타이트(hydroxyapatite)에 흡착시켜 복합항균제를 제조하였다. 질산은의 농도, 온도, 압력, 숙성시간에 따른 흡착된 은이온양의 변화를 관찰하였고, 은-수산화아파타이트 흡착의 최적조건을 얻었다. 제조된 은-수산화아파타이트를 ICP-MS, SEM-EDAX, DSC, XRD를 이용하여 물리적 화학적 특성을 고찰하였다. 또한 제조된 은-수산화아파타이트는 진탕플라스크실험법(shake flask method, KS M-146-2003)을 이용하여 양성균인 황색포도상구균(staphylococcus aureus, ATCC 6538)과 음성균인 대장균(escherichia coli, ATCC 25922)의 항균성을 확인하였다.

• 한국세라믹학회지
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• 제33권1호
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• pp.7-16
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• 1996

${CO_3}^{2-}$ containing whisker-like hydroxyapatite powders were synthesized byhomogeneous precipitation method using urea, Dicalcium phosphate anhdrate[DCPA; $CaHPO_4$] and octacalcium phosphate [OCP; $Ca_8H_2(PO_4_)6\cdot5H_20$]were obtained as precursors and they transformed to high crystalline hydroxyapatites at pH 5.62, and 6.54 respectively. According to the condition of the final pH in the solutions for the solution products and urea contents OCP was remained. When the solution product of $Ca^{2-}$ and ${PO_4}^{3-}$ was $1.5\times 10^4$[$mM^2$] and the content of urea was 0.25 mol.$dm^{-3}$ well crystallized whisker-like hydroxyapatite tens of micrometer in length was obtained. By heat treatment DCPA and OCP were decomposed into $\beta$-tricalcium phosphate [$\beta$-TCP ; $\beta$-$Ca_3{PO_4}_2$] and $\beta$-dicalcium phosphate [$\beta$-DCP ;$\beta$-$Ca_2P_2O_4}_2$]. And well-crystallized hydroxyapatite was partially decomposed into $\beta$-TCP at $800^{\circ}C$.

• 한국세라믹학회지
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• 제27권8호
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• pp.979-990
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• 1990

The possible use of bioglass as implant materials is due to its biocompatibility to human body. Even if many animal studies for the bioglasses have been performed, their structures and physical properties are not fully understood. In the present work, several investigations such as Raman spectroscopic analysis, density, thermal expansion coefficient, softening temperature, and refractive index measurement were carried out to find the structures and physical properties of bioglasses, where MgO is substituted for CaO in bioglass composition (46.1%SiO2, 24.4%Na2O, 26.9%CaO, 2.6%P2O5 ; mole%). Hydroxyapatite formation on the glass surface reacted in Tris-buffer solution was also examined. When CaO was replaced by MgO, nonbridging oxygen in glass structuer was diminished but the degree of disorder increased. Thermal expansion and softening properties showed the mixed oxide effect. Hydroxyapatite were formed on the surface of 0~11mole% of MgO containing bioglasses, and the thickness of SiO2-rich layer as well as hydroxyapatite layer were unchanged with MgO content. However, the hydroxyapatite was not formed on the surface of the bioglasses containing over 11 mole percent MgO, even if the glasses were reacted for long period.

• 한국세라믹학회지
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• 제28권1호
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• pp.46-52
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• 1991

The hydroxyapatite powders were prepared by the reaction of Ca(CH3COO)2$.$H2O and H3PO4 in aqueous solution. Effect of Ca/P mole ration and pH value on the powder characteristics were investigated. For phosphoric acid was dissociated to PO43- ion above pH 10, the preparation condition of hydroxyapatite by H3PO4 solution had this value. Dried powders were agglomerated each other. The mean agglomerate particle diameter was minimum when the condition was pH 11, Ca/P=1.75 and its specific surface area was 97㎡/g. All powders had poor crystallinity and small CO2. It prevented CaCO3 from using aspirator in preparation and maturing time. In most cases, hydroxyapatite was decomposed into ${\beta}$-TCP at more than 800$^{\circ}C$, into ${\alpha}$-TCP at 1200$^{\circ}C$. However non-decomposed hydroxyapatite was remained in Ca/P=1.85.

• 한국결정성장학회지
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• 제4권3호
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• pp.284-293
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• 1994

분말상의 유기물인 나프탈렌, 파라핀 및 과산화수소 그리고 과산화수소와 함께 염화파라핀을 사용하여 hydroxyapatite 다공체를 제조하고, 그 특성을 검토하였다. 나프탈렌 분말 입자의 양과 크기에 따라 다공체 기공의 크기와 제어가 가능했다. 또한 나프탈렌의 함량이 많아짐에 따라 기공률은 증가하지만 강도는 상대적으로 감소하였다. $H_20_2$를 사용한 경우에는 해면상의 다공체를 얻을 수 있었지만, 기공률 및 성형체의 모양을 제어하기가 어려웠다. 염화파라핀 $H_20_2$를 함께 사용한 경우, 해면상의 다공체는 물론 50% 이상의 높은 기공률의 제어가 가능하였다.

• 한국세라믹학회지
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• 제41권8호
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• pp.628-632
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• 2004

생체친화성 인공골 개발을 위하여 해면골과 매우 유사한 기공구조를 갖는 천연 산호(CaCO$_3$, aragonite phase)를 수열처리하여 수산화아파타이트 다공체를 제조하였다. 생체 친화성을 증진시키기 위하여 산호를 수열 처리하는 과정에서 실리콘을 치환시키는 실험을 하였다. 수열합성과 solvothermal 방법을 반복적으로 사용하여 실리콘이 치환된 수산화아파타이트를 합성하였으며 이들의 각 온도에 따른 상변화 및 실리콘 농도를 XRD, ICP, EDS 등을 통하여 분석하였다. 분석결과로부터 실리콘이 수산화아파타이트 골격 내에 균일하게 분산되어 있음을 확인하였다.

• 한국세라믹학회지
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• 제51권3호
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• pp.145-149
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• 2014

A hydroxyapatite microsphere was prepared using a spray-drying method. The change in the shape as a function of the slurry concentration and the change in the degree of shrinkage according to the heat-treatment temperatures were observed. To obtain biomaterials with improved bio-stability, $CaHPO_4{\cdot}2H_2O$ and $Ca(OH)_2$ were mixed at a ratio of 6 : 4 and then ball-milled to synthesize hydroxyapatite. The hydroxyapatite microsphere was prepared using 30 wt% ~ 80 wt% hydroxyapatite slurry by a spray-drying method. For concentrations lower than 50 wt% or higher than 80 wt%, doughnut-shaped microspheres were produced. However, perfect microspheres were produced when using slurry concentrations of 50 wt% ~ 70 wt%. A dense microstructure was observed after a heat treatment at temperatures higher than $1100^{\circ}C$ and the size was reduced by 24.3% at these temperatures.