Thakur Garima, Singh Amrinder, Singh Inderbir
Department of Pharmaceutics, Chitkara College of Pharmacy, Chitkara University, Patiala-Chandigarh Highway, Rajpura-140401, Patiala, Punjab, India.
Sci Pharm. 2015 Oct 22;84(4):603-617. doi: 10.3390/scipharm84040603.
The present study reports the preparation and evaluation of polymer composites of chitosan and montmorillonite. The prepared polymer composites were evaluated for various powder properties and characterized by FTIR-ATR (Fourier Transform Infrared Spectroscopy- Attenuated Total Reflectance), XRD (X Ray Diffraction), and SEM (Scaning Electron Microscopy) techniques. Heckel and Kawakita equations indicated good compression characteristics of the composites. The polymer composites were employed in formulating sustained release tablets of aceclofenac. The formation of intercalated lamellar structures due to the entrapment of clay particles in the polymeric matrix network was found to be responsible for the drug release retardant behavior of the composites. The in vitro drug release data were fitted to various models like zero-order, first-order, Higuchi, Korsmeyer-Peppas, and Hixon and Crowell for studying the mechanism of drug release from the formulation. The value of release exponent (n) was found to range between 0.59 and 0.82, indicating non-Fickian (anomalous) drug release behavior. Swelling-induced diffusion of the drug through the polymer matrix and polymer matrix chain relaxation appeared to play a role in the release of the drug from the polymer composites.
本研究报告了壳聚糖与蒙脱石聚合物复合材料的制备与评价。对制备的聚合物复合材料的各种粉末性质进行了评价,并通过傅里叶变换红外光谱-衰减全反射(FTIR-ATR)、X射线衍射(XRD)和扫描电子显微镜(SEM)技术进行了表征。Heckel方程和Kawakita方程表明复合材料具有良好的压缩特性。该聚合物复合材料被用于制备醋氯芬酸缓释片。发现由于粘土颗粒被困在聚合物基体网络中而形成的插层层状结构是复合材料药物释放延迟行为的原因。体外药物释放数据拟合了零级、一级、Higuchi、Korsmeyer-Peppas以及Hixon和Crowell等各种模型,以研究药物从制剂中释放的机制。发现释放指数(n)的值在0.59至0.82之间,表明药物释放行为为非Fickian(异常)。药物通过聚合物基体的溶胀诱导扩散和聚合物基体链松弛似乎在药物从聚合物复合材料中的释放中起作用。