Shiohira Hideo, Fujii Makiko, Koizumi Naoya, Kondoh Masuo, Watanabe Yoshiteru
Department of Pharmaceutics and Biopharmaceutics, Showa Pharmaceutical University, 3-3165 Higashi-Tamagawagakuen, Machida-Shi, Tokyo 194-8543, Japan.
Int J Pharm. 2009 Sep 8;379(1):119-24. doi: 10.1016/j.ijpharm.2009.06.017. Epub 2009 Jun 23.
The aim of this study was to develop a new chronotherapeutic pharmaceutical preparation as a sustained-release suppository for prevention and therapeutic use against bronchial asthma in the early morning. Sustained-release hollow-type (SR-HT) suppositories using sodium alginate (Alg-Na), sodium polyacrylate (PANa) or polyacrylate-PANa co-polymer (PA-PANa) as gelling polymers (gel agent) were prepared and pharmaceutical characteristics of these suppositories were investigated. Type A SR-HT suppositories comprised a suppository shell prepared with oleaginous base and containing aminophylline only or aminophylline with Alg-Na or PANa in the cavity (hollow space). Type B SR-HT suppositories comprised a suppository shell prepared with oleaginous base and gel agent (30%), with aminophylline in the hollow space. In drug-release studies, the acrylate polymer-containing suppositories showed linearity of delayed release rate, providing significantly decreased the highest concentration of theophylline in plasma (C(max)) and delayed the time required to reach C(max) (t(max)) and the mean residence time (MRT) after rectal administrated in rabbits. In particular, suppositories containing PA-PANa maintained significantly higher theophylline concentrations than control suppositories at 12h after rectal administration. Furthermore, histopathological examination indicated that these suppositories using acrylate polymers did not result in rectal lesions. The SR-HT suppository, particularly using PA-PANa as a gel agent, may thus be useful against nocturnal symptoms of asthma. In this study, we confirmed new formulation of sustained-release suppository for chronotherapy of theophylline using oily base material in combination with polymer such as PA-PANa. The hollow-type suppository containing oleaginous base and hydrophilic polymer in the shell could be useful device for rectal administration of various drugs with prolongation of plasma concentration.
本研究的目的是开发一种新的时辰治疗药物制剂,作为一种缓释栓剂,用于在清晨预防和治疗支气管哮喘。制备了以海藻酸钠(Alg-Na)、聚丙烯酸钠(PANa)或聚丙烯酸-PANa共聚物(PA-PANa)作为胶凝聚合物(凝胶剂)的缓释空心型(SR-HT)栓剂,并研究了这些栓剂的药学特性。A型SR-HT栓剂包括一个用油性基质制备的栓剂壳,其腔(中空空间)中仅含有氨茶碱或含有氨茶碱与Alg-Na或PANa。B型SR-HT栓剂包括一个用油性基质和凝胶剂(30%)制备的栓剂壳,中空空间中有氨茶碱。在药物释放研究中,含丙烯酸酯聚合物的栓剂显示出延迟释放速率的线性关系,直肠给药后,血浆中茶碱的最高浓度(C(max))显著降低,达到C(max)所需的时间(t(max))和平均驻留时间(MRT)延迟。特别是,含有PA-PANa的栓剂在直肠给药12小时后,茶碱浓度显著高于对照栓剂。此外,组织病理学检查表明,这些使用丙烯酸酯聚合物的栓剂不会导致直肠病变。因此,SR-HT栓剂,特别是使用PA-PANa作为凝胶剂的栓剂,可能对哮喘的夜间症状有效。在本研究中,我们证实了使用油性基础材料与PA-PANa等聚合物联合用于茶碱时辰治疗的缓释栓剂新剂型。壳中含有油性基质和亲水性聚合物的空心型栓剂可能是一种有用的装置,可用于直肠给药各种药物,延长血浆浓度。