• 제목/요약/키워드: dicalcium phosphate

검색결과 46건 처리시간 0.017초

Calcium Phosphate Bone Cement Based on Wet Prepared Dicalcium Phosphate

  • Chang, Myung Chul
    • 한국세라믹학회지
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    • 제55권5호
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    • pp.480-491
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    • 2018
  • Calcium phosphates (CaP) were prepared by a wet chemical method. Micro-crystalline dicalcium phosphate (DCPD) was precipitated at $37^{\circ}C$ and pH 5.0 using $Ca(OH)_2$ and $H_3PO_4$. The precipitated DCPD solution was kept at $37^{\circ}C$ for 96 h. Artificial bone cement was composed of DCPD, $Ca(H_2PO_4)_2{\cdot}H_2O$ (MCPM), and $CaSO_4{\cdot}1/2H_2O$, $H_2O$ and aqueous poly-phosphoric acid solution. The wet prepared CaP powder was used as a matrix for the bone cement recipe. With the addition of aqueous poly-phosphoric acid, the cement hardening reaction was started and the CaP bone cement blocks were fabricated for the mechanical strength measurement. For the tested blocks, the mechanical strength was measured using a universal testing machine, and the microstructure phase analysis was done by field emission scanning electron microscopy and X-ray diffraction. The cement hardening reaction occurred through the decomposition and recrystallization of MCPM and $CaSO_4{\cdot}1/2H_2O$ added on the surface of the wet prepared CaP, and this resulted in grain growth in the bone cement block.

Amputation level for hard tissue formation in pulp with tetracalcium / dicalcium phosphate compound.

  • Yoshikawa, M.;Toda, T.
    • 대한치과보존학회:학술대회논문집
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    • 대한치과보존학회 2001년도 추계학술대회(제116회) 및 13회 Workshop 제3회 한ㆍ일 치과보존학회 공동학술대회 초록집
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    • pp.566.1-566
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    • 2001
  • The most desirable healing process for endodontic therapy is apical closure by hard tissue such as dentine or cementum. Then, we estimated hard tissue conductivity of tetracalcium phosphate (4CP)/dicalcium phosphate (2CP) compound using mandibular first molars of SD rats. Residual pulp responses to the calcium phosphate compound were examined at several amputation levels of pulp. 2CP was purchased and passed through a $32-\mu\textrm{m}$ sieve. 4CP was obtained from a stoichiometric mixture of 2CP and calcium carbonate (Mol ratio: Ca/P=2.0) by the dry synthetic method at 1, 400(C for 8 hours.(omitted)

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치아 연마용 인산일수소칼슘의 합성 및 물리화학적 성질 (Synthesis and Physico-Chemical Properties of Dicalcium Phosphate Dihydrate for Dental Abrasive)

  • 서성수;황성주;이기명;이계주
    • 약학회지
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    • 제37권1호
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    • pp.66-75
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    • 1993
  • Dental abrasive, dicalcium phosphate dehydrate (DCPD) was prepared and the several important factors affecting on the quality of toothpaste were investigated by means of set test, glycerine absorption, Coulter counter test, color difference, BET adsorption, mercury porosimetery, and rheogram comparing with two foreign DCPDs, MFO4 and Dentphos K. Sample DCPD was prepared by reaction between 85% H$_{3}$PO$_{4}$ and 15% milk of lime at $39^{\circ}C$ (pH6.5), and stabilized with TSPP and TMP. The physicochemical properties of Sample DCPD were obtained as follows: whiteness (98.99), average particle size (15.5 $\mu\textrm{m}$), pH (7.9), remainder particle weight (0.49w/w%), glycerine absorption value (64 ml), and set test (passed). N$_{2}$ adsorption curves (BET) of three kinds of DCPD showed non-porous type III isotherm. BET adsorption parameters of sample DCPD showed that surface area was 24.9 m$^{2}$/g, total pore volume 0.09 cm$^{3}$/g and average pore radius 72.0 $\AA$. The rheogram of the toothpaste containing each DCPD showed bulged plastic flow with yield vlaue and thixotropic behavior. These results meet standard requirements as abrasive standard, and suggested that synthesized sample DCPD could be used a dental abrasive such as a high quality grade in practice as foreign DCPDs.

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Dicalcium Phosphate Dihydrate를 함유한 3.5% 과산화수소가 치아표면에 미치는 영향 (Effects of 3.5% Hydrogen Peroxide Containing Dicalcium Phosphate Dihydrate on the Tooth Enamel Surface)

  • 심연수
    • 치위생과학회지
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    • 제12권4호
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    • pp.320-328
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    • 2012
  • 본 연구는 3.5% 과산화수소(hydrogen peroxide, HP)에 dicalcium phosphate dihydrate (DCPD)를 함유한 치아미백제가 치아 미백과 표면 특성에 미치는 영향에 대해 연구하였다. 발치한 건전한 소구치 30개를 치아 시편으로 하였고, 이 시편을 3군(A1, A2, A3)으로 나누었다(n=10). 3.5% HP에 DCPD를 0 g(대조군, A1), 0.1 g(A2), 1 g(A3)을 함유시켜 치아 미백제를 제조했다. 모든 군은 하루에 8시간 미백하여 14일 동안 반복하였다. 미백제의 pH 측정, 유도 결합플라스마 원자 방출 분광기(ICP-AES)를 이용한 원소분석을 실시하고, 법랑질의 색, 경도, 표면의 형태 및 무기질 성분을 측정하였고, ANOVA를 이용하여 분석하였다. 1. 치아미백제의 pH를 측정한 결과 DCPD를 함유한 치아미백제의 pH는 함유하지 않은 치아미백제의 pH에 비해 증가를 보였으나 통계적으로 유의한 차이는 없었다(p>.05). 2. 치아미백제의 무기질 함량을 측정한 결과 DCPD 농도가 증가할수록 칼슘과 인의 농도가 증가했으며, Ca/P 비는 1.1~1.2 정도로 나타났다. 3. 모든 군에서 $L^*$ 값은 미백 후가 미백 전에 비해 통계적으로 유의하게 증가했다(p<.05). 4. 치아의 경도는 미백 후가 미백 전에 비해 통계적으로 유의하게 미세경도의 감소를 보였다(p<.05). 하지만 DCPD함유량이 증가할수록 대조군에 비해 실험군의 미세경도 감소율이 적게 나타났다. 5. 미백 후 법랑질 표면의 형태는 대조군에서 표면의 다공성과 침식 현상이 보였으나(A1), DCPD 함유량이 가장 높은 군(A3)에서는 표면 변화가 나타나지 않았다. 6. 미백 후 법랑질 표면의 성분은 DCPD 함유량이 증가할수록 Ca, P 함량이 증가하였다. 이상의 결과로부터 DCPD를 함유한 3.5% HP의 치아미백제는 대조군과 동등한 치아미백 효과가 있고, pH를 상승시켜서 치아 표면의 탈회를 감소시키며 법랑질의 표면 형태와 성분 변화에 덜 영향을 줌으로써, 치아미백제의 구성성분으로 실용화할 수 있을 것으로 생각된다.

서로 다른 인 공급원들의 생물학적 이용율과 어린 육계의 능력에 미치는 영향 (Effects of Dietary Supplemental Phosphate from Different Sources on Performance of Young Broiler Chicks and It's Biological Availability)

  • 류경선
    • 한국가금학회지
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    • 제23권4호
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    • pp.169-175
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    • 1996
  • An experiment was conducted with male broiler chicks to determine the effect of different dietary phosphorus sources and evaluate the biological availability of phosphorus sources. The biological availability of phosphorus from dicalcium phosphate (DCP) was used as a reference standard (100%) compared to defluorinate phosphate (DFP). DCP and DFP was supplemented to a corn-soy basal diet at levels of 0.05, 0.15, 0.25, 0.35%. Each of 24 pens of 10 male broiler chicks with three replications was used for three weeks. The results indicated that weight gain, feed in-take, feed efficiency, nonphytic phosphorus (NPP) and tibia ash were significantly different among treatments. Dietary supplemental phosphorus of DFP improved weight gain, NPP intake and feed efficiency consistently, whereas supplements of DCP did not show consistent increase. Regression equations was used for the availability of DPP compared with DCP when percent bone ash was a function of total phosphorus in the diet. The percent (%) bone ash of DFP groups compared to that of DCP groups showed a value of 59.98% as a slope ratio. DFP indicated lower biological availability compared to DCP, but it's dietary supplementation tended to increase bone ash and maximize the growth of young broiler chicks.

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균일침전법을 이용항 Hydroxyapatite 분말의 제조 및 가열변화 (Synthesis of Hydroxyapatite Powders by Homogeneous Precipitation Method and Their Thermal Changes)

  • 이진호;박훈;김창은
    • 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 $800^{\circ}C$.

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Chemical characteristics of mineral trioxide aggregate and its hydration reaction

  • Chang, Seok-Woo
    • Restorative Dentistry and Endodontics
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    • 제37권4호
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    • pp.188-193
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    • 2012
  • Mineral trioxide aggregate (MTA) was developed in early 1990s and has been successfully used for root perforation repair, root end filling, and one-visit apexification. MTA is composed mainly of tricalcium silicate and dicalcium silicate. When MTA is hydrated, calcium silicate hydrate (CSH) and calcium hydroxide is formed. Formed calcium hydroxide interacts with the phosphate ion in body fluid and form amorphous calcium phosphate (ACP) which finally transforms into calcium deficient hydroxyapatite (CDHA). These mineral precipitate were reported to form the MTA-dentin interfacial layer which enhances the sealing ability of MTA. Clinically, the use of zinc oxide euginol (ZOE) based materials may retard the setting of MTA. Also, the use of acids or contact with excessive blood should be avoided before complete set of MTA, because these conditions could adversely affect the hydration reaction of MTA. Further studies on the chemical nature of MTA hydration reaction are needed.

생체활성 유리 골 시멘트의 응결 및 수산화 아파타이트 형성 (Setting and Hydroxyapatite Formation of Bioactive Glass Bone Cement)

  • 임형봉;김철영
    • 한국세라믹학회지
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    • 제42권11호
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    • pp.770-776
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    • 2005
  • Hardening and hydroxyapatite(HAp) formation behavior of the bioactive cements in the system of $CaO-SiO_{2}-P_{2}O_{5}$ glasses and the corresponding glass-ceramics were studied. DCPD (Dicalcium Phosphate Dihydrate: $CaHPO_4{\cdot}2H_2O$) and DCPA (Dicalcium Phosphate Anhydrous: $CaHPO_4$) were developed when the prepared glass and glass-ceramic powders were mixed with three different solutions. The DCPD and DCPA transformed to HAp when the cement was soaked in Simulated Body Fluid (SBF), and this HAp formation strongly depended on the releasing capacity of $Ca^{2+}$ ions from the cements. The glass-ceramic containing apatite showed fast setting, but no HAp formation was observed because no $Ca^{2+}$ ions were released from this glass-ceramics. The compressive strength of the cements increased with reaction time in SBF until all DCPD and DCPA transformed to HAp.

Highly efficient adsorptive removal of uranyl ions from aqueous solutions using dicalcium phosphate nanoparticles as a superabsorbent

  • Saghatchi, Hadis;Ansari, Reza;Mousavi, H. Zavvar
    • Nuclear Engineering and Technology
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    • 제50권7호
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    • pp.1112-1119
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    • 2018
  • Dicalcium phosphate nanoparticles (DCP-NPs) was synthesized chemically and used for adsorptive removal of uranyl ions from aqueous solutions in a batch system. A commercial grade of DCP (monetite) was also employed for comparison. The synthesized and commercial adsorbents (S-DCP and C-DCP) were characterized by FT-IR, SEM and XRD techniques. The investigation of adsorption isotherms indicated that the maximum adsorption capacities ($q_m$) for C-DCP and S-DCP were 714.3 and $666.7mg\;g^{-1}$ (at 293 K), respectively. The experimental kinetics were well-described by the pseudo-second-order kinetic and the equilibrium data were fitted with both Langmuir and Freundlich adsorption models. Thermodynamic studies indicated that the adsorption of uranyl ions on the monetite surface was a spontaneous exothermic process. The exhausted adsorbents could be regenerated by washing with $0.10mol\;L^{-1}$ NaOH.

Gliclazide compatibility with some common chemically reactive excipients; using different analytical techniques

  • Jabbari, Hamideh Najjarpour;Shabani, Mohammad;Monajjemzadeh, Farnaz
    • 분석과학
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    • 제34권2호
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    • pp.46-55
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    • 2021
  • Evaluation of drug-excipient compatibility is one of the basic steps in the preformulation of pharmaceutical dosage forms. Some reactive excipients have been known so far which may cause stability problems for drug molecules in pharmaceutical dosage forms. The aim of this study was to evaluate drugexcipient compatibility of gliclazide with some common pharmaceutical excipients, known for their ability to incorporate in drug-excipient interactions. Binary mixtures were prepared using lactose, magnesium stearate, polyvinylpyrrolidone, sodium starch glycolate, polyethylene glycol 2000 and dicalcium phosphate. Based on the results; gliclazide was incompatible with all tested excipients; but not with dicalcium phosphate. DSC (Differential Scanning Calorimetry) results were in accordance with HPLC (High Pressure liquid chromatography) data and were more predictive than FTIR (Fourier Transform Infrared Spectroscopy). Drug and reactive excipients incompatibility was fully discussed and documented. It is advisable to avoid incompatible excipients or carefully monitor the drug stability when incorporating such excipients in final formulation designs.