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An Ammonia-Induced Calcium Phosphate Nanostructure: A Potential Assay for Studying Osteoporosis and Bone Metastasis

机译:氨诱导的磷酸钙纳米结构:用于研究骨质疏松症和骨转移的潜在测定

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Osteoclastic resorption of bones plays a central role in both osteoporosis and bone metastasis. A reliable in vitro assay that simulates osteoclastic resorption in vivo would significantly speed up the process of developing effective therapeutic solutions for those diseases. Here, we reported the development of a novel and robust nanostructured calcium phosphate coating with unique functions on the track-etched porous membrane by using an ammonia-induced mineralization (AiM) technique. The calcium phosphate coating uniformly covers one side of the PET membrane, enabling testing for osteoclastic resorption. The track-etched pores in the PET membrane allow calcium phosphate mineral pins to grow inside, which, on the one hand, enhances coating integration with a membrane substrate and, on the other hand, provides diffusion channels for delivering drugs from the lower chamber of a double-chamber cell culture system. The applications of the processed calcium phosphate coating were first demonstrated as a drug screening device by using alendronate, a widely used drug for osteoporosis. It was confirmed that the delivery of alendronate significantly decreased both the number of monocyte-differentiated osteoclasts and coating resorption. To demonstrate the application in studying bone metastasis, we delivered a PC3 prostate cancer-conditioned medium and confirmed that both the differentiation of monocytes into osteoclasts and the osteoclastic resorption of the calcium phosphate coating were significantly enhanced. This novel assay thus provides a new platform for studying osteoclastic activities and assessing drug efficacy in vitro.
机译:破骨细胞骨吸收在骨质疏松症和骨转移中起着核心作用。在体内模拟破骨细胞再吸收的可靠体外试验将显著加快为这些疾病开发有效治疗方案的进程。在这里,我们报道了利用氨诱导矿化(AiM)技术在径迹蚀刻多孔膜上开发出一种新型且坚固的纳米结构磷酸钙涂层,该涂层具有独特的功能。磷酸钙涂层均匀地覆盖PET膜的一侧,从而能够检测破骨细胞的再吸收。PET膜中的轨迹蚀刻孔允许磷酸钙矿质针在内部生长,这一方面增强了涂层与膜基质的整合,另一方面,为从双室细胞培养系统的下室输送药物提供了扩散通道。通过使用广泛用于治疗骨质疏松症的药物阿仑膦酸盐,处理后的磷酸钙涂层首次被证明是一种药物筛选设备。经证实,阿仑膦酸盐的输送显著降低了单核细胞分化破骨细胞的数量和涂层吸收。为了证明其在骨转移研究中的应用,我们提供了PC3前列腺癌条件培养基,并证实单核细胞分化为破骨细胞和破骨细胞对磷酸钙涂层的再吸收均显著增强。因此,这种新的检测方法为体外研究破骨细胞活性和评估药物疗效提供了一个新的平台。

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