Desai Kashappa Goud
School of Life Sciences and Biotechnology, Korea University, Seoul, South Korea.
J Biomater Appl. 2007 Jan;21(3):217-33. doi: 10.1177/0885328206056771. Epub 2006 Jan 27.
This study reports the properties of tableted microparticles based on high-amylose corn starch (HACS)-pectin blend polymers as the controlled release system for diclofenac sodium (DS). HACS-pectin blend microparticles are prepared through a modified process by the spray drying technique, which is a widely used microencapsulation technique in the pharmaceutical industry. The mean particle size of various formulations of blend microparticles is in the range of 5.8-7.3 mum. Fourier transform infrared (FTIR) spectroscopy study reveals the absence of well-defined interaction between HACS-pectin and polymers-DS. The blend microparticles thus prepared were compressed into tablets using the directly compressible excipients. A cross-sectional view of the tablet reveals the presence of nearly spherical shaped particles in the tablet, suggesting that the system chosen is ideal for tableting. In vitro drug release study indicates that tableted microparticulate system is found to be suitable for the manipulation of release behavior for DS in the gastrointestinal tract. Release mechanism of the DS from tableted microparticles is by Fickian diffusion since the value of n approaches 0.5.
本研究报道了基于高直链玉米淀粉(HACS)-果胶共混聚合物的压片微粒作为双氯芬酸钠(DS)控释系统的性能。HACS-果胶共混微粒通过喷雾干燥技术的改良工艺制备,喷雾干燥技术是制药行业广泛使用的微囊化技术。共混微粒各种配方的平均粒径在5.8 - 7.3微米范围内。傅里叶变换红外(FTIR)光谱研究表明HACS-果胶与聚合物-DS之间不存在明确的相互作用。如此制备的共混微粒使用直接可压性辅料压制成片。片剂的横截面视图显示片剂中存在近球形颗粒,表明所选择的系统对于压片是理想的。体外药物释放研究表明,压片微粒系统适用于控制DS在胃肠道中的释放行为。由于n值接近0.5,DS从压片微粒中的释放机制是菲克扩散。