Rao Y M, Veni J K, Jayasagar G
Centre for Biopharmaceutics and Pharmacokinetics, University College of Pharmaceutical Sciences, Kakatiya University, Warangal, AP, India.
Drug Dev Ind Pharm. 2001 Sep;27(8):759-66. doi: 10.1081/ddc-100107239.
Controlled-release tablets (having near zero-order release) of diclofenac sodium, a water-soluble drug, were prepared using hydrophilic polymers like hydroxypropylmethylcellulose (HPMC), sodium carboxymethylcellulose (NaCMC), and Carbopol 934. Tablets were also prepared with mixtures of polymers of NaCMC, HPMC, and Carbopol 934. The optimum ratio of drug: HPMC. NaCMC was found to be 1:2:1. A combination of nonionic polymer HPMC and anionic NaCMC polymer matrix resulted in near zero-order release of diclofenac sodium. The results obtained were in agreement with the earlier reports. It is observed that increasing polymer content produces more sustained effect. A combination of nonionic polymer HPMC and anionic polymer NaCMC as the polymer matrix resulted in near zero-order release of diclofenac sodium. Drug release from the matrix did not follow Fick's law of 'diffusion and exhibited near zero-order release. Results of the bioavailability studies indicated that formulation 4 with drug:HPMC:NaCMC equal to 1:2:1 was similar to the marketed product Dicloran SR and showed better bioavailability than Voveran SR. A statistically significant difference was seen between Voveran SR and the other two products. A good in vitro-in vivo correlation was observed for these products.
使用羟丙基甲基纤维素(HPMC)、羧甲基纤维素钠(NaCMC)和卡波姆934等亲水性聚合物制备了水溶性药物双氯芬酸钠的控释片(具有接近零级释放特性)。还制备了含有NaCMC、HPMC和卡波姆934聚合物混合物的片剂。发现药物与HPMC、NaCMC的最佳比例为1:2:1。非离子聚合物HPMC和阴离子NaCMC聚合物基质的组合导致双氯芬酸钠接近零级释放。所得结果与早期报告一致。观察到聚合物含量增加会产生更持久的效果。非离子聚合物HPMC和阴离子聚合物NaCMC作为聚合物基质的组合导致双氯芬酸钠接近零级释放。药物从基质中的释放不遵循菲克扩散定律,呈现接近零级释放。生物利用度研究结果表明,药物:HPMC:NaCMC等于1:2:1的制剂4与市售产品双氯芬酸钠缓释片相似,且比扶他林缓释片具有更好的生物利用度。扶他林缓释片与其他两种产品之间存在统计学上的显著差异。观察到这些产品具有良好的体外-体内相关性。