Dpto. Química en Ciencias Farmacéuticas (Unidad de Química Inorgánica y Bioinorgánica), Facultad de Farmacia, Universidad Complutense de Madrid, Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), 28040 Madrid, Spain; Centro de Investigación Biomédica en Red de Bioingeniería, Biomateriales y Nanomedicina (CIBER-BBN), Spain.
Dpto. Química en Ciencias Farmacéuticas (Unidad de Química Inorgánica y Bioinorgánica), Facultad de Farmacia, Universidad Complutense de Madrid, Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), 28040 Madrid, Spain.
Acta Biomater. 2019 Mar 1;86:441-449. doi: 10.1016/j.actbio.2019.01.013. Epub 2019 Jan 14.
3D porous scaffolds based on agarose and nanocrystalline apatite, two structural components that act as a temporary mineralized extracellular matrix, were prepared by the GELPOR3D method. This shaping technology allows the introduction of thermally-labile molecules within the scaffolds during the fabrication procedure. An angiogenic protein, Vascular Endothelial Growth Factor, and an antibiotic, cephalexin, loaded in mesoporous silica nanoparticles, were included to design multifunctional scaffolds for bone reconstruction. The dual release of both molecules showed a marked increase in the number of blood vessels on embryonic day 14 in chicken embryos grown ex ovo, while, at the same time providing an antibiotic local concentration capable of inhibiting Staphylococcus aureus bacterial growth. In this sense, different release patterns, monitored by UV-spectroscopy, could be tailored as a function of the cephalexin loading strategy, either releasing all the loaded cephalexin in the first 4 h or less than 50% after 24 h. The scaffold surface was characterized by a high hydrophilicity, with contact angles between 50° and 63°, which enabled the adhesion and proliferation of preosteoblastic cells. STATEMENT OF SIGNIFICANCE: The localized delivery of bioactive molecules has attracted significant attention due to the potential for dose reduction as well as reduced side effects compared to systemic delivery. In this article multifunctional 3D porous scaffolds with a designed porosity have been fabricated. The method also enables the controlled loading of an antibiotic drug and an angiogenic protein into the scaffold. These scaffolds, whose composition resembles the extracellular matrix are suitable for the adhesion of preosteoblast cells, exhibit a sustained cephalexin delivery adequate for inhibiting bacterial growth as well as release the proangiogenic molecule which induces blood vessel formation in chicken embryos grown ex ovo.
基于琼脂糖和纳米晶磷灰石的 3D 多孔支架,这两种结构成分可作为临时矿化细胞外基质,通过 GELPOR3D 方法制备。这种成型技术允许在制造过程中向支架内引入热敏分子。血管内皮生长因子(一种血管生成蛋白)和载于介孔硅纳米粒子中的头孢菌素(一种抗生素)被负载到支架中,以设计用于骨重建的多功能支架。这两种分子的双重释放显示出,在鸡胚体外培养的胚胎第 14 天,血管数量明显增加,同时提供了一种能够抑制金黄色葡萄球菌生长的局部抗生素浓度。在这种意义上,通过紫外光谱监测到的不同释放模式,可以根据头孢菌素的负载策略进行定制,要么在最初的 4 小时内释放所有负载的头孢菌素,要么在 24 小时后释放不到 50%。支架表面的高亲水性,接触角在 50°到 63°之间,这使得成骨前体细胞能够黏附和增殖。
与全身给药相比,生物活性分子的局部给药因其潜在的减少剂量和降低副作用而引起了广泛关注。在本文中,我们制备了具有设计孔隙率的多功能 3D 多孔支架。该方法还能够将抗生素药物和血管生成蛋白受控地负载到支架中。这些支架的组成类似于细胞外基质,适合成骨前体细胞的黏附,表现出持续的头孢菌素释放,足以抑制细菌生长,并释放促血管生成分子,从而诱导鸡胚体外培养的血管形成。