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多孔羟磷灰石和明胶/羟磷灰石微球的制备。

Porous hydroxyapatite and gelatin/hydroxyapatite microspheres obtained by calcium phosphate cement emulsion.

机构信息

Biomaterials, Biomechanics, and Tissue Engineering Group, Department of Materials Science and Metallurgy, Technical University of Catalonia, Avda. Diagonal 647, E-08028 Barcelona, Spain.

出版信息

J Biomed Mater Res B Appl Biomater. 2011 Apr;97(1):156-66. doi: 10.1002/jbm.b.31798. Epub 2011 Feb 2.

Abstract

Hydroxyapatite and hybrid gelatine/hydroxyapatite microspheres were obtained through a water in oil emulsion of a calcium phosphate cement (CPC). The setting reaction of the CPC, in this case the hydrolysis of α-tricalcium phosphate, was responsible for the consolidation of the microspheres. After the setting reaction, the microspheres consisted of an entangled network of hydroxyapatite crystals, with a high porosity and pore sizes ranging between 0.5 and 5 μm. The size of the microspheres was tailored by controlling the viscosity of the hydrophobic phase, the rotation speed, and the initial powder size of the CPC. The incorporation of gelatin increased the sphericity of the microspheres, as well as their size and size dispersion. To assess the feasibility of using the microspheres as cell microcarriers, Saos-2 cells were cultured on the microspheres. Fluorescent staining, SEM studies, and LDH quantification showed that the microspheres were able to sustain cell growth. Cell adhesion and proliferation was significantly improved in the hybrid gelatin/hydroxyapatite microspheres as compared to the hydroxyapatite ones.

摘要

通过磷酸钙水泥(CPC)的水包油乳液获得了羟基磷灰石和混合明胶/羟基磷灰石微球。在这种情况下,CPC 的凝固反应,即 α-磷酸三钙的水解,负责微球的固结。凝固反应后,微球由羟基磷灰石晶体的缠结网络组成,具有高孔隙率和 0.5 至 5 μm 之间的孔径。通过控制疏水性相的粘度、转速和 CPC 的初始粉末尺寸来调整微球的尺寸。明胶的掺入增加了微球的球形度以及它们的尺寸和尺寸分散度。为了评估将微球用作细胞微载体的可行性,将 Saos-2 细胞培养在微球上。荧光染色、SEM 研究和 LDH 定量表明,微球能够维持细胞生长。与羟基磷灰石微球相比,混合明胶/羟基磷灰石微球显著提高了细胞黏附和增殖。

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