Goonasekera Chandhi S, Jack Kevin S, Cooper-White Justin J, Grøndahl Lisbeth
School of Chemistry and Molecular Biosciences, The University of Queensland, St. Lucia, QLD 4072, Australia.
J Mater Chem B. 2013 Nov 14;1(42):5842-5852. doi: 10.1039/c3tb21110j. Epub 2013 Oct 1.
Nano-sized hydroxyapatite (HAP) is of interest in biomaterials science due to its similarity to bone mineral. In this study, HAP modification using 3-aminopropyltriethoxysilane (APTES) was carried out in toluene and the effect of reaction time and curing temperature on the surface layers formed was investigated through X-ray photoelectron spectroscopy, Fourier transform infrared (FT-IR) and solid-state nuclear magnetic resonance (NMR) spectroscopy. It is shown that the chemical composition is strongly influenced by the curing temperature; with low temperatures of 50 and 100 °C resulting in a fully condensed APTES layer, an intermediate temperature of 150 °C causing partial oxidation of the surface layer with the conversion of some amine functionality to amides while curing at a temperature of 200 °C additionally leads to thermal decomposition of the silane layer and a loss of the pendent amine groups. However, the stability of these particles in aqueous solution indicated a loss of the silane layer for samples cured at 150 °C or less and it is concluded that there is a trade-off between the availability of functionality for further chemical grafting and the stability for these APTES-modified HAP materials. Subsequent attachment of the polyelectrolyte poly(acrylic acid) (PAA) via both ionic interaction and covalent bonding using carbodiimide chemistry resulted in particles with more negative zeta potentials (-27 to -18 mV) compared to pure HAP, which were stable to dispersion in aqueous solution, both with respect to their chemical composition at the particle surface and to aggregation.
纳米级羟基磷灰石(HAP)因其与骨矿物质的相似性而在生物材料科学领域备受关注。在本研究中,使用3-氨丙基三乙氧基硅烷(APTES)在甲苯中对HAP进行改性,并通过X射线光电子能谱、傅里叶变换红外(FT-IR)光谱和固态核磁共振(NMR)光谱研究了反应时间和固化温度对所形成表面层的影响。结果表明,化学组成受固化温度的强烈影响;50和100°C的低温导致APTES层完全缩合,150°C的中间温度导致表面层部分氧化,一些胺官能团转化为酰胺,而在200°C固化时还会导致硅烷层热分解和侧链胺基团损失。然而,这些颗粒在水溶液中的稳定性表明,在150°C或更低温度下固化的样品会损失硅烷层,并且得出结论,对于这些APTES改性的HAP材料,在进一步化学接枝的官能团可用性和稳定性之间存在权衡。随后,通过离子相互作用和使用碳二亚胺化学的共价键合连接聚电解质聚丙烯酸(PAA),与纯HAP相比,得到了具有更负的zeta电位(-27至-18 mV)的颗粒,这些颗粒在水溶液中的分散体在颗粒表面的化学组成和聚集方面都是稳定的。