Kumar Pramod, Singh Sanjay, Mishra Brahmeshwar
Department of Pharmaceutics, Institute of Technology, Banaras Hindu University, Varanasi, India.
Chem Pharm Bull (Tokyo). 2008 Sep;56(9):1234-42. doi: 10.1248/cpb.56.1234.
Colon targeted delivery systems of metronidazole (MTZ) based on osmotic technology were developed. The developed systems consisted of osmotic core (drug, osmotic agent and wicking agent), coated with semipermeable membrane (SPM) containing guar gum as pore former, coated core were then further coated with enteric coating to protect the system from acidic environment of stomach. The effect of various formulation variables namely the level of wicking agent (sodium lauryl sulphate), osmotic agent in the osmotic core, the level of pore former (guar gum) in SPM, and the thickness of SPM, were studied on physical parameters and drug release characteristics of developed formulations. MTZ release was inversely proportional to SPM thickness, but directly related to the level of pore former, wicking agent and osmotic agent. On the other hand burst strength of the exhausted shells was decreased with the increase in level of pore former in the membrane but increased with the increase in the thickness of SPM. The drug release from the developed formulations was independent of pH, and agitation intensity, but dependent on the osmotic pressure of the release media. The thickness of enteric coating could prevent formation of delivery pores before contact with simulated colonic fluid, but had no effect on drug release. Result of SEM studies showed the formation of in-situ delivery pores in the membrane from where the drug release occurred, and the number of pores formed were directly related to the initial level of pore former (guar gum) in SPM. The manufacturing procedure was found to be reproducible and formulations were found to be stable during 3 months of accelerated stability studies.
研发了基于渗透技术的甲硝唑(MTZ)结肠靶向给药系统。所研发的系统由渗透芯(药物、渗透剂和吸湿剂)组成,外包覆有含瓜尔胶作为致孔剂的半透膜(SPM),然后对包衣芯进一步进行肠溶包衣,以保护系统免受胃酸性环境的影响。研究了各种制剂变量,即吸湿剂(十二烷基硫酸钠)水平、渗透芯中的渗透剂、SPM中致孔剂(瓜尔胶)水平以及SPM厚度对所研发制剂的物理参数和药物释放特性的影响。MTZ释放与SPM厚度成反比,但与致孔剂、吸湿剂和渗透剂水平直接相关。另一方面,排空外壳的破裂强度随着膜中致孔剂水平的增加而降低,但随着SPM厚度的增加而增加。所研发制剂中的药物释放与pH和搅拌强度无关,但取决于释放介质的渗透压。肠溶包衣厚度可防止在与模拟结肠液接触前形成给药孔,但对药物释放无影响。扫描电子显微镜研究结果表明,膜中形成了原位给药孔,药物从这些孔中释放出来,形成的孔数量与SPM中致孔剂(瓜尔胶)的初始水平直接相关。发现制造工艺具有可重复性,并且在3个月的加速稳定性研究期间制剂被发现是稳定的。