Umamaheshwari R B, Jain Subheet, Bhadra Dipankar, Jain N K
Pharmaceutics Research Laboratory, Department of Pharmaceutical Sciences, Dr Hari Singh Gour University, Sagar (M.P.) 470 003, India.
J Pharm Pharmacol. 2003 Dec;55(12):1607-13. doi: 10.1211/0022357022223.
This investigation is part of our ongoing effort to develop effective drug delivery systems for the treatment of Helicobacter pylori infection using polycarbonate (PC) floating microspheres as drug carriers. In an effort to augment the anti-H. pylori effect of acetohydroxamic acid (AHA), floating PC microspheres, which have the ability to reside in the gastrointestinal (GI) tract for an extended period, were prepared by emulsion (O/W) solvent evaporation technique. The effect of PC concentration on the morphology, particle size, entrapment efficiency and drug release rate was studied. In-vitro studies confirmed the excellent floating properties of PC microspheres. In-vitro and in-vivo growth inhibition studies were performed on developed system(s) taking isolated cultures of H. pylori and H. pylori-infected Mongolian gerbils, respectively. The drug and PC microspheres both showed anti-H. pylori activity in vivo, but the required dose of AHA was effectively reduced by a factor of 10 in the case of PC microspheres. In conclusion, the floating microspheres more effectively cleared H. pylori from the GI tract than the drug because of the prolonged gastric residence time resulting from the excellent buoyancy of the PC.
本研究是我们正在进行的工作的一部分,旨在开发以聚碳酸酯(PC)漂浮微球为药物载体治疗幽门螺杆菌感染的有效给药系统。为了增强乙酰氧肟酸(AHA)的抗幽门螺杆菌作用,采用乳液(水包油)溶剂蒸发技术制备了能够在胃肠道(GI)中长期停留的漂浮PC微球。研究了PC浓度对其形态、粒径、包封率和药物释放速率的影响。体外研究证实了PC微球具有优异的漂浮性能。分别以分离培养的幽门螺杆菌和幽门螺杆菌感染的蒙古沙鼠为对象,对所开发的系统进行了体外和体内生长抑制研究。药物和PC微球在体内均表现出抗幽门螺杆菌活性,但在PC微球的情况下,所需的AHA剂量有效地降低了10倍。总之,由于PC优异的浮力导致胃内停留时间延长,漂浮微球比药物更有效地从胃肠道清除幽门螺杆菌。