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首页> 外文期刊>Journal of Materials Chemistry, B. materials for biology and medicine >Reverse-biomineralization assembly of acid-sensitive biomimetic fibers for hard tissue engineering and drug delivery
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Reverse-biomineralization assembly of acid-sensitive biomimetic fibers for hard tissue engineering and drug delivery

机译:酸敏感仿生纤维的反向生物矿化组件,用于硬组织工程和药物输送

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Biomimetic design and fabrication of tissue-engineered bone scaffolds that not only resemble natural bone in structure and performance, but also are endowed with specific functions, e.g., for drug delivery, are always an exciting research area. Herein, we report a kind of doxorubicin hydrochloride-loaded biomimetic ultrathin fiber, which is synthesized by preparing a kind of nanoporous bioactive glass fiber as a drug/protein carrier and bio-template and combining them in a reverse-biomineralization reaction. Protein adsorption experiments demonstrate that bovine serum albumin can be hosted in open large nanopores of bioactive glass fibers and the adsorption mechanism follows the intraparticle diffusion process. Biomineralization shows that proteins and drugs can be integrated at the nanoscale into minerals to form biomimetic and drug-loaded fibers, and the formation of such fibers depends on the functional ion (Ca, P, and Si) release of bioactive glass fibers and electrostatic interaction among bioactive glass fibers, proteins, and drugs. The drug-loaded composite fibers demonstrate bare homogeneous solid matrices in the fiber interior and surfaces upon which amorphous carbonated apatite resides. The drug release profiles show that the as-synthesized fibers are acid-sensitive and drugs can be released at pH 5, but not at neutral pH 7.4. Because of their structural advantages and the characteristics of acid-sensitive drug release, the biomimetic fibers have potential applications for repairing the bone defects resulting from tumour extirpation.
机译:组织工程化骨支架的仿生设计和制造不仅在结构和性能上类似于天然骨骼,而且具有特定功能,例如用于药物输送,一直是令人兴奋的研究领域。本文中,我们报道了一种载有盐酸阿霉素的仿生超薄纤维,它是通过制备一种纳米多孔生物活性玻璃纤维作为药物/蛋白质载体和生物模板,并通过反向生物矿化反应将它们组合而合成的。蛋白质吸附实验表明,牛血清白蛋白可以存在于生物活性玻璃纤维的大开口纳米孔中,并且其吸附机制遵循颗粒内扩散过程。生物矿化表明蛋白质和药物可以在纳米级整合到矿物质中以形成仿生纤维和载药纤维,而这种纤维的形成取决于生物活性玻璃纤维的功能性离子(Ca,P和Si)释放和静电相互作用生物活性玻璃纤维,蛋白质和药物。载有药物的复合纤维在纤维内部和无定形碳酸磷灰石所驻留的表面上显示出裸露的均匀固体基质。药物释放曲线表明合成后的纤维对酸敏感,药物可以在pH 5释放,但在中性pH 7.4不能释放。由于它们的结构优势和酸敏感性药物释放的特性,仿生纤维在修复因肿瘤切除而导致的骨缺损方面具有潜在的应用。

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