Karavas Evangelos, Ktistis Georgios, Xenakis Aristotelis, Georgarakis Emmanouel
Department of Pharmaceutical Technology, School of Pharmacy, Aristotle University of Thessaloniki, Greece.
Drug Dev Ind Pharm. 2005 Jul;31(6):473-89. doi: 10.1080/03639040500215958.
In the present study, solid dispersion systems of felodipine (FEL) with polyvinylpyrrolidone (PVP) were developed, in order to enhance solid state stability and release kinetics. The prepared systems were characterized by using Differential Scanning Calorimetry, X-Ray Diffraction, and Scanning Electron Microscopy techniques, while the interactions which take place were identified by using Fourier Transformation-Infrared Spectroscopy. Due to the formation of hydrogen bonds between the carbonyl group of PVP and the amino groups of FEL, transition of FEL from crystalline to amorphous state was achieved. The dispersion of FEL was found to be in nano-scale particle sizes and dependent on the FEL/PVP ratio. This modification leads to partial miscibility of the two components, as it was verified by DSC and optimal glass dispersion of FEL into the polymer matrix since no crystalline structure was detected with XRD. The above deformation has a significant effect on the dissolution enhancement and the release kinetics of FEL, as it causes the pattern to change from linear to logarithmic. An impressive optimization of the dissolution profile is observed corresponding to a rapid release of FEL in the system containing 10% w/w of FEL, releasing 100% in approximately 20 min. The particle size of dispersed FEL into PVP matrix could be classified as the main parameter affecting dissolution optimization. The mechanism of such enhancement consists of the lower energy required for the dissolution due to the amorphous transition and the fine dispersion, which leads to an optimal contact surface of the drug substance with the dissolution media. The prepared systems are stable during storage at 40 +/- 1 degrees C and relative humidity of 75 +/- 5%. Addition of sodium docusate as surfactant does not affect the release kinetics, but only the initial burst due to its effect on the surface tension and wettability of the systems.
在本研究中,开发了非洛地平(FEL)与聚乙烯吡咯烷酮(PVP)的固体分散体系统,以提高固态稳定性和释放动力学。通过差示扫描量热法、X射线衍射和扫描电子显微镜技术对制备的系统进行了表征,同时利用傅里叶变换红外光谱法确定了发生的相互作用。由于PVP的羰基与FEL的氨基之间形成了氢键,实现了FEL从结晶态到非晶态的转变。发现FEL的分散体为纳米级粒径,且取决于FEL/PVP比例。这种改性导致两种组分部分互溶,这通过差示扫描量热法得到验证,并且FEL在聚合物基质中实现了最佳玻璃态分散,因为X射线衍射未检测到晶体结构。上述转变对FEL的溶出增强和释放动力学有显著影响,因为它使模式从线性变为对数。观察到溶出曲线有令人印象深刻的优化,对应于含10% w/w FEL的系统中FEL的快速释放,在约20分钟内释放100%。分散在PVP基质中的FEL的粒径可被归类为影响溶出优化的主要参数。这种增强的机制包括由于非晶态转变和精细分散而使溶出所需能量降低,这导致药物与溶出介质的接触表面达到最佳。制备的系统在40±1℃和75±5%的相对湿度下储存期间是稳定的。添加十二烷基磺酸钠作为表面活性剂不影响释放动力学,但由于其对系统表面张力和润湿性的影响,仅影响初始突释。