Sharma Abhinav, Kumar Bimlesh, Singh Sachin Kumar, Gulati Monica, Vaidya Yogyata, Rathee Harish, Ghai Deepak, Malik Adil Hussain, Yadav Ankit Kumar, Maharshi Peddi, Bawa Palak, Rajesh Sarvi Yadav, Sharma Parth, Pandey Narendra Kumar, Mohanta Souvik
School of Pharmaceutical Sciences, Lovely Professional University, Phagwara, Punjab-144 411, India.
Curr Drug Deliv. 2018;15(3):367-387. doi: 10.2174/1567201815666171207165059.
Polysaccharide based delivery systems have been successfully used to target drugs to colon. In some recent reports, the superiority of concomitant administration of probiotics with such systems has been established. However, the pharmacokinetics of such symbiotic therapy remain unexplored hitherto.
This study deciphers the pharmacokinetic parameters of guar gum based colon targeted spheroids of sulfasalazine with co-administration of probiotics in experimental rats. Thirty rats were divided into five groups using Latin square design. These were subjected to treatment with delayed release formulation, uncoated spheroids, coated spheroid and coated spheroids along with probiotics.
In case of delayed release formulation, negligible presence of sulfasalazine in plasma was observed in first 2h, followed by significant increase in sulfasalazine concentration after 3h. Higher plasma concentrations of sulfasalazine were detected for uncoated spheroids with and without probiotics. Negligible release of drug upto 5h and delayed Tmax in case of guar-gum coated sulfasalazine spheroids with or without probiotics clearly indicated successful formulation of colon targeted spheroids. Further, for coated spheroids (both with and without probiotics), the value of Tmax is found to be significantly higher than those with the other treatments.
Colon targeted spheroids were therefore, found to reduce absorption of drug which, in turn, is expected to reduce the side effects as only local action in colon is required for treatment of colitis. This is the first report on pharmacokinetic study of a colon targeted delivery system co-administered with probiotics.
基于多糖的给药系统已成功用于将药物靶向输送至结肠。在最近的一些报道中,已证实此类系统与益生菌联合给药具有优势。然而,迄今为止,这种共生疗法的药代动力学仍未得到探索。
本研究解读了柳氮磺胺吡啶的瓜尔胶基结肠靶向球体与益生菌联合给药在实验大鼠体内的药代动力学参数。采用拉丁方设计将30只大鼠分为五组。这些大鼠分别接受缓释制剂、未包衣球体、包衣球体以及包衣球体与益生菌联合治疗。
对于缓释制剂,在最初2小时血浆中柳氮磺胺吡啶的含量可忽略不计,3小时后柳氮磺胺吡啶浓度显著增加。无论有无益生菌,未包衣球体的柳氮磺胺吡啶血浆浓度均较高。无论有无益生菌,瓜尔胶包衣的柳氮磺胺吡啶球体在5小时内药物释放可忽略不计且达峰时间延迟,这清楚地表明成功制备了结肠靶向球体。此外,对于包衣球体(无论有无益生菌),发现其达峰时间值显著高于其他治疗组。
因此,发现结肠靶向球体可减少药物吸收,进而有望减少副作用,因为治疗结肠炎仅需在结肠局部起作用。这是关于与益生菌联合给药的结肠靶向给药系统药代动力学研究的首篇报道。