Saravanan Muniyandy, Sri Nataraj Kalakonda, Ganesh Kettavarampalayam Swaminath
Department of Pharmaceutics, Vel's College of Pharmacy, Chennai-600117, India.
Chem Pharm Bull (Tokyo). 2003 Aug;51(8):978-83. doi: 10.1248/cpb.51.978.
The object of this study was to develop hydroxypropyl methylcellulose (HPMC) based cephalexin extended release tablet, which can release the drug for six hours in predetermined rate. Twenty-one batches of cephalexin tablets were prepared by changing various physical and chemical parameters, in order to get required theoretical release profile. The influences of HPMC, microcrystalline cellulose powder (MCCP), granulation technique, wetting agent and tablet hardness on cephalexin release from HPMC based extended release tablets were studied. The formulated tablets were also characterized by physical and chemical parameters. The dissolution results showed that a higher amount of HPMC in tablet composition resulted in reduced drug release. Addition of MCCP resulted in faster drug release. Tablets prepared by dry granulation was released the drug slowly than the same prepared with a wet granulation technique. Addition of wetting agent in the tablets prepared with dry granulation technique showed slower release. An increase in tablet hardness resulted in faster drug release. Tablets prepared with a wet granulation technique and having a composition of 9.3% w/w HPMC with a hardness of 10-12 kg/cm(2) gave predicted release for 6 h. The in vitro release data was well fit in to Higuchi and Korsmeyer-Peppas model. Physical and chemical parameters of all formulated tablets were within acceptable limits. One batch among formulated twenty-one batches was successful and showed required theoretical release. The effect of storage on in vitro release and physicochemical parameters of successful batch was studied and was found to be in acceptable limits.
本研究的目的是开发基于羟丙基甲基纤维素(HPMC)的头孢氨苄缓释片,该片剂能够以预定速率释放药物达6小时。通过改变各种物理和化学参数制备了21批头孢氨苄片剂,以获得所需的理论释放曲线。研究了HPMC、微晶纤维素粉末(MCCP)、制粒技术、润湿剂和片剂硬度对基于HPMC的缓释片中头孢氨苄释放的影响。还对所制备片剂的物理和化学参数进行了表征。溶出结果表明,片剂配方中较高含量的HPMC会导致药物释放减少。添加MCCP会使药物释放更快。干法制粒制备的片剂比湿法制粒制备的片剂药物释放慢。在干法制粒技术制备的片剂中添加润湿剂显示释放较慢。片剂硬度增加会导致药物释放更快。采用湿法制粒技术制备、含有9.3% w/w HPMC且硬度为10 - 12 kg/cm²的片剂实现了6小时的预期释放。体外释放数据很好地符合Higuchi模型和Korsmeyer - Peppas模型。所有制备片剂的物理和化学参数均在可接受范围内。在制备的21批片剂中有一批成功,并显示出所需的理论释放。研究了储存对成功批次的体外释放和理化参数的影响,发现其在可接受范围内。