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首页> 外文期刊>Journal of biomedical materials research. Part B, Applied biomaterials. >In vitro and in vivo degradation of biomimetic octacalcium phosphate and carbonate apatite coatings on titanium implants
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In vitro and in vivo degradation of biomimetic octacalcium phosphate and carbonate apatite coatings on titanium implants

机译:钛植入物上仿生八磷酸钙和碳酸盐磷灰石涂层的体外和体内降解

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Calcium phosphate (Ca-P) coatings have been applied onto titanium alloys prosthesis to combine the srength of metals with the bioactivity of Ca-P. It has been clearly shown in many publications that Ca-P coating accelerates bone formation around the implant. However, longevity of the Ca-P coating for an optimal bone apposition onto the prosthesis remains controversial. Biomimetic bonelike carbonate apatite (BCA) and Octacalcium Phosphate (OCP) coatings were deposited on Ti6Al4V samples to evaluate their in vitro and in vivo dissolution properties. The coated plates were soaked in alpha-MEM for 1, 2, and 4 weeks, and they were analyzed by Back Scattering Electron Microscopy (BSEM) and by Fourier Transform Infra Red spectroscopy (FTIR). Identical coated plates were implanted subcutaneously in Wistar rats for similar periods. BSEM, FTIR, and histomorphometry were performed on the explants. In vitro and in vivo, a carbonate apatite (CA) formed onto OCP and BCA coatings via a dissolution-precipitation process. In vitro, both coatings dissolved overtime, whereas in vivo BCA calcified and OCP partially dissolved after 1 week. Thereafter, OCP remained stable. This different in vivo behavior can be attributed to (1) different organic compounds that might prevent or enhance Ca-P dissolution, (2) a greater reactivity of OCP due to its large open structure, or (3) different thermodynamic stability between OCP and BCA phases. These structural and compositional differences promote either the progressive loss or calcification of the Ca-P coating and might lead to different osseointegration of coated implants.
机译:磷酸钙(Ca-P)涂层已应用于钛合金假体上,以结合金属的持久性和Ca-P的生物活性。在许多出版物中已经清楚地表明,Ca-P涂层可加速植入物周围的骨形成。但是,Ca-P涂层在假体上获得最佳骨骼附着的寿命仍存在争议。将仿生的骨样碳酸盐磷灰石(BCA)和磷酸八钙(OCP)涂层沉积在Ti6Al4V样品上,以评估其体外和体内溶出特性。将涂覆的板在α-MEM中浸泡1、2和4周,并通过反向散射电子显微镜(BSEM)和傅里叶变换红外光谱(FTIR)对其进行分析。将相同的涂层板皮下植入Wistar大鼠皮下相似的时间。在外植体上进行BSEM,FTIR和组织形态测定。在体外和体内,碳酸钙磷灰石(CA)通过溶解沉淀过程形成在OCP和BCA涂层上。在体外,两种包衣都随时间溶解,而在1周后,体内BCA钙化,OCP部分溶解。此后,OCP保持稳定。这种不同的体内行为可归因于(1)可能阻止或增强Ca-P溶解的不同有机化合物,(2)由于其开放结构大而使OCP具有更高的反应性,或(3)OCP与BCA阶段。这些结构和组成上的差异会促进Ca-P涂层的逐渐消失或钙化,并可能导致涂层植入物的骨整合不同。

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