Jain Sunil K, Haider Tanweer, Kumar Amrish, Jain Akhlesh
Department of Pharmaceutics, Institute of Pharmaceutical Sciences, Guru Ghasidas Vishwavidyalaya (A Central University), Bilaspur, C.G., 495 009, India.
AAPS PharmSciTech. 2016 Oct;17(5):1131-40. doi: 10.1208/s12249-015-0443-5. Epub 2015 Nov 13.
Helicobacter pylori infection remains challenging as it mainly colonized beneath the deep gastric mucosa and adheres to epithelial cells of the stomach. Concanavalin-A (Con-A)-conjugated gastro-retentive poly (lactic-co-glycolic acid) (PLGA) nanoparticles of acetohydroxamic acid (AHA) and clarithromycin (CLR) were prepared and evaluated under in vitro conditions. Solvent evaporation method was employed for preparation of nanoparticles and characterized for particle size distribution, surface morphology, percent drug entrapment, and in vitro drug release in simulated gastric fluid. Optimized nanoparticles were conjugated with Con-A and further characterized for Con-A conjugation efficiency and mucoadhesion and tested for in vitro anti-H. pylori activity. The conjugation with Con-A further sustained the drug release over a period of 8 h when compared to non-conjugated nanoparticles of AHA and CLR. In vitro anti H. pylori study confirmed that Con-A-conjugated nanoparticles containing both drugs, i.e., CLR and AHA, had shown maximum zone of inhibition compared to other formulations. In a nut shell, results suggest that the developed systems could be used for better therapeutic activity against H. pylori infection.
幽门螺杆菌感染仍然具有挑战性,因为它主要定植于胃黏膜深层并粘附于胃上皮细胞。制备了伴刀豆球蛋白A(Con-A)偶联的乙酰氧肟酸(AHA)和克拉霉素(CLR)的胃滞留型聚乳酸-乙醇酸共聚物(PLGA)纳米颗粒,并在体外条件下进行了评估。采用溶剂蒸发法制备纳米颗粒,并对其粒径分布、表面形态、药物包封率以及在模拟胃液中的体外药物释放进行了表征。将优化后的纳米颗粒与Con-A偶联,并进一步对Con-A偶联效率和粘膜粘附进行表征,同时测试其体外抗幽门螺杆菌活性。与未偶联的AHA和CLR纳米颗粒相比,与Con-A偶联可使药物在8小时内持续释放。体外抗幽门螺杆菌研究证实,与其他制剂相比,含有CLR和AHA两种药物的Con-A偶联纳米颗粒显示出最大的抑菌圈。简而言之,结果表明所开发的系统可用于更好地治疗幽门螺杆菌感染。