• 한국세라믹학회지
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• 제35권3호
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• pp.209-218
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• 1998

세라믹스계 생체재료중에서 그 화학조성과 결정구조가 사람의 뼈와 매우 유사하여, 다른 재료보다 생체진화성이 월등히 우수한 수산화 아파타이트 분말을 용액침전법으로 제조하였다. 이때 용액침전법의 가장 큰 단점인 칼슘결손의 발생을 억제하고, 아울러 질소대신 공기중에서도 화학양론조성의 수산화 아파타이트 원료분말을 쉽게 합성할 수 있는 방법을 개발하였다. 즉, 공기중에 존재하는 CO2 기체로부터 형성된 반응용액중에 {{{{ {CO }`_{3 } ^{2- } }} 이온의 농도를 pH를 이용 조절함으로써 침전반응 및 여과공정을 공기중에서 수행하면서도 Ca의 결손이 없고 소결성이 매우 우수한 수산화 아파타이트 분말을 제조할 수 있었다.

• 한국세라믹학회지
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• 제26권1호
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• pp.123-131
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• 1989

Hydroxyapatite powders were syntehsized by the reaction of Ca(NO3)2.4H2O and (NH4)2HPO4 in aqueous solution. The effect of the Ca/P mole ratio in the starting solution on the sintering of the powders and its microstructure was studied. When the Ca/P mole ratio in the starting solution was 1.69, the relative density of the sintered bodies was more than 95%. The sinterability was decreased as the Ca/P mole ratio in the starting solution was increased (Ca/P mole ratio >1.67). Hydroxyapatite sintered bodies obtained from the Ca/P mole ratio=1.69 had very excellent bending strength. The best bending strength was obtained at 110$0^{\circ}C$ and its value was 1220kg/$\textrm{cm}^2$. The average grain size was 0.277${\mu}{\textrm}{m}$. Most of sintered bodies were almost shown 100% hydroxyapatite phase. However, in case of the Ca/P mole ratio=1.64 hydroxyapatite was decomposed to $\alpha$-whitlockite above 120$0^{\circ}C$.

• 한국세라믹학회지
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• 제40권12호
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• pp.1154-1158
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• 2003

Hydrothermal deposition of hydroxyapatite coatings on $Al_2$O$_3$ substrates was studied using aqueous solutions of Ca(NO$_3$)$_2$ㆍ4$H_2O$ and (NH$_4$)$_2$HPO$_4$ containing EDTA disodium salt as a chelating agent for $Ca^{2+}$. For the precipitation of the coatings the EDTA-Ca$^{2+}$ chelates were dissociated thermally at 20$0^{\circ}C$ or decomposed by oxidation with $H_2O$$_2$ at 9$0^{\circ}C$. Scanning electron microscopy and X-ray diffraction were used to investigate the deposition behavior and the phase of the coatings. Hydroxyapatite coatings were not deposited with the thermal dissociation method, whereas uniform deposition of the coatings (about 0.7 $\mu\textrm{m}$ thickness) was obtained with the oxidative decomposition method. The coatings consisted of fine rod-like hydroxyapatite crystals (hexagonal structure) with 60-80 nm diameters, having some preferred orientation with their length (i.e., the c axis) perpendicular to the substrate.ate.

• Journal of Periodontal and Implant Science
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• 제24권1호
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• pp.185-195
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• 1994

This study was conducted to evaluate the healing potential of hydroxyapatite and demineralized freeze dried bone in 5 dogs. Chronic periodontitis was induced by ligating elastic wire randomized as follows. The group in which only flap operation was performed was used as control. The group in which flap operation using nonresorbable nonporous hydroxyapatite (Orthomatrix)was performed was used as experimental I. The group which flap operation using resorbable porous hydroxyapatite (Biocoral) was performed as experimental II. The group in which flap operation using demineralized freeze-dried bone was performed was used as experimental III. Thereafter dogs serially sacrificed at the 1,2,4 and 8 weeks and the specimens were prepared, and stained with Hematoxilin-Eosin stain for the light microscopic evaluation. The results of the this study were as follows : 1. Control group : progressive inflammatory cell infiltration till 4 weeks and epithelial undergrowth. 2. Group I. : epithelial undergrowth and new bone formed with fibrous margin around HA granule. 3. Group II. : no epithelial undergrowth and direct bone formation at the porous granule 4. Group III. : could not see epithelial undergrowth but obviously new cementum formation.

• 한국세라믹학회지
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• 제33권9호
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• pp.1003-1011
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• 1996

Hydroxyapatite powder was synthesized by a citrate method, . Char-like precursor composed of Ca8(HPO4)2(PO4)4.5H2O (OCP) and CaCo3 was found via viscous resin-like intermediate by heating the mixed aqueous solution of Ca(NO3)2.4H2O(NH4)2HPO4 and citric acid. Resulted powder was transformed into hydroxyapatite phase by firing over 120$0^{\circ}C$-135$0^{\circ}C$ for 4 hr using the powder calcined at 90$0^{\circ}C$ for 10 hr composed of mostly single hydroxyapatite phase. The sintered densities increased with firing temperature up to 130$0^{\circ}C$ but the highest relative density was about 94% of theoritical value. indicating the presence of closed pores. The maximum 96 MPa of flexural strength was obtained at 120$0^{\circ}C$ firing but the flexural strength showed lower values over the above sintering condition. Vitro test was performed by immersing of two jointed specimens in SBF for seven days and adhesion was observed between two specimens.

• 한국세라믹학회지
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• 제28권5호
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• pp.373-382
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• 1991

The effect of Ca/P mole ratio (Ca/P=1.60, 1.67, 1.75) in the initial solution on the mechanical properties of alumina added hydroxyapatite was investigated. Hydroxyapatite was synthesized by precipitation method using Ca(NO3)2$.$4H2O and (NH4)2HPO4 as starting materials and 5 wt% of ${\alpha}$-Al2O3 was added to precipitation solution. The powder was calcined at 800$^{\circ}C$ and sintered at 1,150∼1,400$^{\circ}C$ under water vapor atmosphere. With the increasing of Ca/P mole ration in the initial solution, the amount of tricalcium phosphate formed from the decomposition of hydroxyapatite reduced and the sinterability and mechanical properties were increased. The bending strength and Vickers hardness of the specimen sintered at 1,300$^{\circ}C$ with the Ca/P mole ratio of 1.75 in the initial solution were 230 MPa and 650 kg/$\textrm{mm}^2$, respectively. The improvement of mechanical properties was attributed to not only the effect of Ca/P mole ratio but also the strengthening of sintered body by Al substitution for P ions.

• 한국세라믹학회지
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• 제26권2호
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• pp.157-166
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• 1989

The effect of pH variation in starting solution on the characteristics of hydroxyapatite precipitates and powder prepared by the wet method was investigated. Hydroxyapatite precipitates was agglomerated, the average agglomerated particle size was decreased in the range from 2 to 6${\mu}{\textrm}{m}$ with increasing pH values in starting solution. The aspect ratio of rod-shaped hydroxyapatite particle was rapidly increased at pH 11 and 11.5. The maximum specific surface area, 91.1$m^2$/g, was at pH 10.5. Dried powder prepared at high pH values contained more minutes CO2 than that prepared at low pH values. The poor crystallinity was maintained up to $600^{\circ}C$ regardless of the pH values in starting solutions. However, the second phase or high crsytalline hydroxypatite phase appeared above 80$0^{\circ}C$. In pH 9.5 and pH 10, $\beta$-whitlockite transformed to $\alpha$-whitlockite at 120$0^{\circ}C$, while in pH 10.5-11.5, hydroxyapatite phase was maintained up to 120$0^{\circ}C$.

• 한국세라믹학회지
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• 제48권5호
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• pp.412-417
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• 2011

Formation and characterization of hydroxyapatite-based porous ceramics derived from polymer pyroysis were investigated. Polymer based process is chosen for preparing porous hydroxyapatite-based ceramics having a high mechanical strength. The hydroxyapatite-based porous ceramic was prepared by a self-blowing process of a polymethylsiloxane with filler and pyrolyzed at above $1000^{\circ}C$. Biphasic material consisted of hydroxyapatite and CaO has been prepared by solid state reaction from calcium hydroxide($Ca(OH)_2$) and calcium hydrogen phosphate dihydrate($CaHPO_4{\cdot}2H_2O$) as a filler material. The influence of filler content on mechanical properties was evaluated. The change of crystalline phase, microstructure and mechanical properties were investigated and discussed.

• 한국분말야금학회:학술대회논문집
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• 한국분말야금학회 2006년도 Extended Abstracts of 2006 POWDER METALLURGY World Congress Part 1
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• pp.484-485
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• 2006

The process of coprecipitation of biocomposite hydroxyapatite/chitosan from aqueous solution at low temperature in alkali environnement was examined. We have shown that initially we have the formation of amorphous octocalcium phosphates $(Ca_8(HPO_4)(PO_4)_5,\;nH_2O:\;OCP)$ and the transferring from OCP to amorphous calcium phosphate $(Ca_9(PO_4)_3,\;nH_2O:\;TCP)$, and then from TCP to calcium-deficient hydroxyapatite $(Ca_{10-X}\;(HPO_4)_X(PO_4)_{6-x}(OH)_{2-X}\;:\;ACP)$ and hydroxyapatite $(Ca_{10}(PO_4)_6(OH)_2\;:\;HAP)$. The transformation of ACP to HAP was inhibited in the presence of chitosan. The result suggests that there is an affinity binding between ACP and chitosan and subsequently blocking the active growth site of ACP.

• 대한골관절종양학회지
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• 제14권1호
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• pp.25-32
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• 2008

목적: 골종양의 수술적 치료 후 발생한 골결손에 대해 골 대체물의 하나인 Hydroxyapatite ($Bongros^{(R)}$-HA)를 이용하여 치료하고 그 결과를 알아보고자 한다. 대상 및 방법: 2006년 09월부터 2007년 12월까지, 골종양의 수술적 치료 후 발생한 골 결손에 대해 골 대체물의 하나인 Hydroxyapatite를 이용하여 치료하였다. 총 17례의 양성 골종양 환자에서 시행하였으며, 남자 10명, 여자 7명이었고, 평균 연령은 28.5세였다. 양성 골종양의 종류별로 보면 섬유성 이형성증이 8례, 고립성 골 낭종이 5례, 거대 세포종이 4례였다. 부위별로는 근위 대퇴골 6례, 원위 대퇴골 3 례, 근위 경골 3례, 근위 상완골 4례, 골반골 1례였다. 자가골을 함께 사용한 경우가 4례, Hydroxyapatite 단독으로 사용한 경우가 13례였다. 추시 기간은 최단 3 개월에서 최장 15개월로 평균 7.5개월이었다. 주기적인 추시에서 관찰된 단순 방사선 사진에서 Hydroxyapatite의 이식물의 흡수 정도와 골 생성 정도를 술 후 사진과 비교하여 백분율로 표시하여 관찰하였다. 결과: 술 후 평균 4.5 개월에 98% 이상의 흡수율을 관찰할 수 있었고, 술 후 평균 6.2 개월에는 98% 이상의 골 생성을 관찰 할 수 있었다. 골 결손의 양이 적은 겨우 골 형성이 빠른 결과를 보였다(p=0.012). 하지만 그 외 환자의 성별, 나이 그리고 자가골의 첨가 여부에 따른 비교에서 이식물의 흡수율이나 골 생성에 통계학적으로 유의한 차이는 발견할 수 없었으며, 모든 경우에서 최종 추시 시 특이한 합병증은 없었다. 결론: 양성 골종양의 수술적 치료 후 발생한 골 결손의 치료제로서 Hydroxyapatite는 유용할 것으로 사료된다.