CIRIMAT, Université de Toulouse, CNRS, Toulouse INP- ENSIACET, 4 allée Emile Monso, 31030 Toulouse cedex 4, France.
ACS Biomater Sci Eng. 2022 Jun 13;8(6):2363-2374. doi: 10.1021/acsbiomaterials.1c01618. Epub 2022 May 9.
Amorphous calcium phosphate-based materials are of major interest in the field of bone substitution. Very recently, the low-temperature synthesis of a new family of amorphous calcium phosphate containing both orthophosphate and pyrophosphate ions in controlled proportions has been reported. Despite their interest, especially due to the biochemical role and the hydrolysis of pyrophosphate occurring , the behavior of such materials when interacting with aqueous media has never been described. Consequently, we herein report the acellular evolution of three compositions of mixed calcium ortho- and pyrophosphate amorphous materials including a different orthophosphate proportion. As a first step to assess the physicochemical reactivity of these amorphous materials, they were tested in two different media at 37 °C, acidified water and simulated body fluid solution, from 1 h up to 15 days. The results demonstrated that they were quite stable and that they progressively released part of their constitutive ions, highlighting their potential for controlled delivery of bioactive ions (calcium, orthophosphate, and pyrophosphate ions). In addition to these properties, we showed that the material with the highest ortho/(ortho + pyro) phosphate ratio started to crystallize into nanocrystalline apatite analogous to bone mineral within 2 days or 2 weeks depending on the medium. For the other material compositions, no layer of apatite was detected at their surface with SBF testing despite the favorable supersaturation indexes, crystallization being probably inhibited by pyrophosphate ions released in the medium. This varying apatite-forming ability emphasizes the key role of the ortho/(ortho + pyro) phosphate ratio of these materials in their reactivity and bioactivity, which paves the way for the development of this promising family of amorphous calcium phosphate materials with tunable physicochemical and biological properties.
基于无定形磷酸钙的材料在骨替代领域具有重要意义。最近,已经报道了一种新的含正磷酸盐和焦磷酸盐离子的无定形磷酸钙的低温合成方法,可以控制其比例。尽管它们很有意义,特别是由于焦磷酸盐的生化作用和水解作用,但这些材料与水介质相互作用时的行为从未被描述过。因此,我们在此报告了三种混合钙正磷酸盐和焦磷酸盐无定形材料的非细胞进化,其中包括不同的正磷酸盐比例。作为评估这些无定形材料的物理化学反应性的第一步,将它们在两种不同的介质中于 37°C 下进行测试,一种是酸化水,另一种是模拟体液溶液,从 1 小时到 15 天不等。结果表明,它们非常稳定,并且逐渐释放出部分组成离子,突出了它们作为控制释放生物活性离子(钙、正磷酸盐和焦磷酸盐离子)的潜力。除了这些性质外,我们还表明,具有最高正/(正+焦)磷酸盐比例的材料在 2 天或 2 周内(取决于介质)开始结晶成类似于骨矿物质的纳米晶磷灰石。对于其他材料组成,在 SBF 测试中,尽管过饱和度指数有利,但在其表面没有检测到磷灰石层,这可能是由于焦磷酸盐离子在介质中释放而抑制了结晶。这种不同的磷灰石形成能力强调了这些材料的正/(正+焦)磷酸盐比例在其反应性和生物活性中的关键作用,为开发这种具有可调物理化学和生物学性质的有前途的无定形磷酸钙材料铺平了道路。