差示扫描量热法
傅里叶变换红外光谱
核化学
材料科学
纳米颗粒
球霰石
微乳液
动态光散射
碳酸钙
粒径
盐酸环丙沙星
金黄色葡萄球菌
抗菌剂
扫描电子显微镜
化学
色谱法
肺表面活性物质
环丙沙星
化学工程
纳米技术
有机化学
生物化学
抗生素
细菌
遗传学
热力学
复合材料
生物
物理化学
工程类
文石
物理
作者
Solmaz Maleki Dizaj,Farzaneh Lotfipour,Mohammad Barzegar-Jalali,Mohammad Hossein Zarrintan,Khosro Adibkia
标识
DOI:10.3109/21691401.2016.1161637
摘要
Ciprofloxacin HCl-loaded calcium carbonate (CaCO3) nanoparticles were prepared via a w/o microemulsion method and characterized by dynamic light scattering, scanning electron microscopy, X-ray powder diffraction (XRPD) analysis, differential scanning calorimetry (DSC), and Fourier transform infrared spectroscopy (FTIR). The in vitro drug release profiles as well as antimicrobial effect against Staphylococcus aureus (S. aureus) were also evaluated. The antibacterial effect was studied using serial dilution technique to determine the minimum inhibitory concentration (MIC) of the nanoparticles and was confirmed by streak cultures. The mean particle size, drug loading and entrapment efficiency were calculated to be 116.09 nm, 20.49% and 44.05%, respectively. PXRD and FTIR studies confirmed that both vaterite and calcite polymorphs of CaCO3 were formed during the preparation process. In vitro release profiles of the nanoparticles showed slow release pattern for 12 h. The drug-loaded nanoparticles showed similar MICs against S. aureus compared to untreated drug. However, a preserved antimicrobial effect was observed for drug-loaded nanoparticles compared to untreated drug after 2 days of incubation.
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