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Composition and properties of silver-containing calcium carbonate-calcium phosphate bone cement

机译:含银碳酸钙-磷酸钙骨水泥的组成和性能

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摘要

The introduction of silver, either in the liquid phase (as silver nitrate solution: Ag(L)) or in the solid phase (as silver phosphate salt: Ag(S)) of calcium carbonate-calcium phosphate (CaCO_3-CaP) bone cement, its influence on the composition of the set cement (C-Ag(L) and C-Ag(S) cements with a Ca/Ag atomic ratio equal to 10.3) and its biological properties were investigated. The fine characterisation of the chemical setting of silver-doped and reference cements was performed using FTIR spectroscopy. We showed that the formation of apatite was enhanced from the first hours of maturation of C-Ag(L) cement in comparison with the reference cement, whereas a longer period of maturation (about 10 h) was required to observe this increase for C-Ag(S) cement, although in both cases, silver was present in the set cements mainly as silver phosphate. The role of silver nitrate on the setting chemical reaction is discussed and a chemical scheme is proposed. Antibacterial activity tests (5. aureus and 5. epidermidis) and in vitro cytotoxicity tests (human bone marrow stromal cells (HBMSC)) showed that silver-loaded CaCO_3-CaP cements had antibacterial properties (anti-adhesion and anti-biofilm formation) without a toxic effect on HBMSC cells, making C-Ag(S) cement a promising candidate for the prevention of bone implant-associated infections.
机译:以碳酸钙-磷酸钙(CaCO_3-CaP)骨水泥的液相(硝酸银溶液:Ag(L))或固相(磷酸银盐:Ag(S))的形式引入银,研究了其对凝固水泥(Ca / Ag原子比等于10.3的C-Ag(L)和C-Ag(S)水泥)组成的影响及其生物学特性。使用FTIR光谱对掺银水泥和参比水泥的化学定型进行了精细表征。我们显示,与参考水泥相比,从C-Ag(L)水泥熟化的最初几个小时开始,磷灰石的形成得到了增强,而观察到C-Ag(L)水泥的这种增加需要更长的熟化时间(约10小时)。 Ag(S)水泥,尽管在两种情况下,固化水泥中都以磷酸银的形式存在银。讨论了硝酸银在固化化学反应中的作用并提出了化学方案。抗菌活性测试(5.金黄色和5.表皮)和体外细胞毒性测试(人骨髓基质细胞(HBMSC))显示,载银的CaCO_3-CaP水泥具有抗菌性能(抗粘附和抗生物膜形成),而没有对HBMSC细胞具有毒性作用,使C-Ag(S)成为预防骨植入物相关感染的有前途的候选药物。

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  • 来源
    《Journal of materials science 》 |2013年第12期| 2665-2675| 共11页
  • 作者单位

    CIRIMAT, UPS-INPT-CNRS, ENSIACET, Universite de Toulouse, 4, allee Emile Monso, BP 44362, 31030 Toulouse Cedex 4, France;

    Inserm U1026, Bioingenierie Tissulaire, 146 rue Leo Saignat, 33076 Bordeaux Cedex, France ,Universite Bordeaux Segalen, 146 rue Leo Saignat, 33076 Bordeaux Cedex, France;

    LGC, UMR 5503 UPS-INPT-CNRS, Faculte de Pharmacie, Universite de Toulouse, 35 chemin des Maraichers, 31062 Toulouse Cedex 9, France;

    Inserm U1026, Bioingenierie Tissulaire, 146 rue Leo Saignat, 33076 Bordeaux Cedex, France ,Universite Bordeaux Segalen, 146 rue Leo Saignat, 33076 Bordeaux Cedex, France;

    LGC, UMR 5503 UPS-INPT-CNRS, Faculte de Pharmacie, Universite de Toulouse, 35 chemin des Maraichers, 31062 Toulouse Cedex 9, France;

    CIRIMAT, UPS-INPT-CNRS, ENSIACET, Universite de Toulouse, 4, allee Emile Monso, BP 44362, 31030 Toulouse Cedex 4, France;

    CIRIMAT, UPS-INPT-CNRS, ENSIACET, Universite de Toulouse, 4, allee Emile Monso, BP 44362, 31030 Toulouse Cedex 4, France;

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