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The Effect of Polydimethylsiloxane-Ethylcellulose Coating Blends on the Surface Characterization and Drug Release of Ciprofloxacin-Loaded Mesoporous Silica

机译:聚二甲基硅氧烷-乙基纤维素涂料共混物对环丙沙星介孔二氧化硅表面表征和药物释放的影响

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摘要

In this study, we obtained novel solid films composed of ciprofloxacin-loaded mesoporous silica materials (CIP-loaded MCM-41) and polymer coating blends. Polymer coating blends were composed of ethylcellulose (EC) with various levels of polydimethylsiloxane (PDMS, 0, 1, 2% (v/v)). The solid films were prepared via the solvent-evaporation molding method and characterized by using scanning electron microscopy (SEM), optical profilometry, and wettability analyses. The solid-state of CIP present in the solid films was studied using X-ray diffraction (XRD) and differential scanning calorimetry (DSC). The release profiles of CIP were examined as a function of PDMS content in solid films. The surface morphology analysis of solid films indicated the progressive increase in surface heterogeneity and roughness with increasing PDMS content. The contact angle study confirmed the hydrophobicity of all solid films and significant impact of both PDMS and CIP-loaded MCM-41 on surface wettability. DSC and XRD analysis confirmed the presence of amorphous/semi-crystalline CIP in solid films. The Fickian diffusion-controlled drug release was observed for the CIP-loaded MCM-41 coated with PDMS-free polymer blend, whereas zero-order drug release was noticed for the CIP-loaded MCM-41 coated with polymer blends enriched with PDMS. Both the release rate and initial burst of CIP decreased with increasing PDMS content.
机译:在这项研究中,我们获得了由载有环丙沙星的中孔二氧化硅材料(载有CIP的MCM-41)和聚合物涂料共混物组成的新型固体薄膜。聚合物涂料共混物由乙基纤维素(EC)和各种含量的聚二甲基硅氧烷(PDMS,0,1,2%(v / v))组成。通过溶剂蒸发模塑法制备固体膜,并通过使用扫描电子显微镜(SEM),光学轮廓测定法和润湿性分析来表征。使用X射线衍射(XRD)和差示扫描量热法(DSC)研究了固态膜中存在的CIP的固态。检查了CIP的释放曲线与固体膜中PDMS含量的关系。固体膜的表面形态分析表明,随着PDMS含量的增加,表面异质性和粗糙度逐渐增加。接触角研究证实了所有固体膜的疏水性,以及PDMS和CIP负载的MCM-41对表面润湿性的显着影响。 DSC和XRD分析证实了固体膜中存在无定形/半结晶CIP。对于不含PDMS的聚合物共混物的CIP负载MCM-41,观察到Fickian扩散控制的药物释放,而对于富含PDMS的聚合物共混物的CIP负载MCM-41,则观察到零级药物释放。随着PDMS含量的增加,CIP的释放速率和初始爆发均降低。

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