Gupta College of Technological Sciences, Ashram More, Asansol-1, India.
Arch Pharm Res. 2010 Apr;33(4):575-83. doi: 10.1007/s12272-010-0412-1. Epub 2010 Apr 27.
The purpose of the study was to develop a multiunit sustained release dosage form of diltiazem hydrochloride using a natural polymer, sodium carboxymethyl xanthan gum and polyethyleneimine (PEI) from a completely aqueous environment. PEI treated diltiazem resin complex loaded beads were characterized by morphology, drug entrapment efficiency, in vitro and in vivo release behaviour. 40% and 80% drug was released in 2 hour in pH 1.2 and in 5 to 6 h in pH 6.8 respectively depending on the formulation variables. The prolonged release was attributed to decreased swelling of the beads due to PEI treatment. Maintaining the shape throughout the dissolution process, PEI treated diltiazem resin complex beads released the drug following non-Fickian transport phenomena. In vivo pharmacokinetic evaluation in rabbits shows slow and prolonged drug release when compared with diltiazem solution. The designed beads are suitable for prolonged release of a water soluble drug under a complete aqueous environment using natural gum.
本研究旨在开发一种盐酸地尔硫卓的多单位缓释剂型,使用天然聚合物羧甲基黄原胶和聚乙烯亚胺(PEI),完全在水相环境中进行。PEI 处理的盐酸地尔硫卓树脂复合物载药丸通过形态、药物包封效率、体外和体内释放行为进行了表征。根据制剂变量,40%和 80%的药物分别在 pH1.2 下 2 小时和 pH6.8 下 5-6 小时内释放。由于 PEI 处理,珠子的肿胀减少,导致释放延长。PEI 处理的盐酸地尔硫卓树脂复合物珠在整个溶解过程中保持形状,遵循非菲克扩散规律释放药物。与盐酸地尔硫卓溶液相比,在兔子体内的药代动力学评价显示出药物释放缓慢且持续时间长。设计的珠子适用于在完全水相环境中使用天然胶进行水溶性药物的长效释放。