Skwira Adrianna, Szewczyk Adrian, Prokopowicz Magdalena
Department of Physical Chemistry, Faculty of Pharmacy, Medical University of Gdańsk, Hallera 107, Gdańsk 80-416, Poland.
Polymers (Basel). 2019 Sep 4;11(9):1450. doi: 10.3390/polym11091450.
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% (/)). 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.
在本研究中,我们制备了由负载环丙沙星的介孔二氧化硅材料(负载CIP的MCM-41)和聚合物涂层混合物组成的新型固体薄膜。聚合物涂层混合物由含有不同含量聚二甲基硅氧烷(PDMS,0、1、2%(/))的乙基纤维素(EC)组成。通过溶剂蒸发成型法制备固体薄膜,并使用扫描电子显微镜(SEM)、光学轮廓仪和润湿性分析对其进行表征。使用X射线衍射(XRD)和差示扫描量热法(DSC)研究固体薄膜中CIP的固态。研究了CIP在固体薄膜中的释放曲线与PDMS含量的关系。固体薄膜的表面形态分析表明,随着PDMS含量的增加,表面不均匀性和粗糙度逐渐增加。接触角研究证实了所有固体薄膜的疏水性以及PDMS和负载CIP的MCM-41对表面润湿性的显著影响。DSC和XRD分析证实了固体薄膜中存在无定形/半结晶的CIP。对于涂有无PDMS聚合物混合物的负载CIP的MCM-41,观察到菲克扩散控制的药物释放,而对于涂有富含PDMS的聚合物混合物的负载CIP的MCM-41,观察到零级药物释放。随着PDMS含量的增加,CIP的释放速率和初始突释均降低。