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Release behavior and toxicity profiles towards A549 cell lines of ciprofloxacin from its layered zinc hydroxide intercalation compound

机译:环丙沙星层状插层化合物对环丙沙星A549细胞系的释放行为和毒性谱

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Background Layered hydroxides salts (LHS), a layered inorganic compound is gaining attention in a wide range of applications, particularly due to its unique anion exchange properties. In this work, layered zinc hydroxide nitrate (LZH), a family member of LHS was intercalated with anionic ciprofloxacin (CFX), a broad spectrum antibiotic via ion exchange in a mixture solution of water:ethanol. Results Powder x-ray diffraction (XRD), Fourier transform infrared (FTIR) and thermogravimetric analysis (TGA) confirmed the drug anions were successfully intercalated in the interlayer space of LZH. Specific surface area of the obtained compound was increased compared to that of the host due to the different pore textures between the two materials. CFX anions were slowly released over 80 hours in phosphate-buffered saline (PBS) solution due to strong interactions that occurred between the intercalated anions and the host lattices. The intercalation compound demonstrated enhanced antiproliferative effects towards A549 cancer cells compared to the toxicity of CFX alone. Conclusions Strong host-guest interactions between the LZH lattice and the CFX anion give rise to a new intercalation compound that demonstrates sustained release mode and enhanced toxicity effects towards A549 cell lines. These findings should serve as foundations towards further developments of the brucite-like host material in drug delivery systems.
机译:背景技术层状氢氧化物盐(LHS)是一种层状无机化合物,在广泛的应用中受到关注,特别是由于其独特的阴离子交换特性。在这项工作中,LHS的家庭成员硝酸氢氧化锌(LZH)层与阴离子环丙沙星(CFX)(一种广谱抗生素)通过在水:乙醇的混合溶液中进行离子交换而插入。结果粉末X射线衍射(XRD),傅立叶变换红外光谱(FTIR)和热重分析(TGA)证实了药物阴离子已成功插入LZH层间空间。由于两种材料之间的孔结构不同,因此与主体相比,所得化合物的比表面积增加。由于插层阴离子与主体晶格之间发生强烈的相互作用,CFX阴离子在磷酸盐缓冲盐水(PBS)溶液中历经80个小时缓慢释放。与单独的CFX毒性相比,该插层化合物对A549癌细胞具有增强的抗增殖作用。结论LZH晶格和CFX阴离子之间强烈的主客体相互作用产生了一种新型插层化合物,该化合物表现出缓释模式并增强了对A549细胞系的毒性作用。这些发现应作为进一步发展药物输送系统中类似水镁石基质材料的基础。

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