Arora Saahil, Gupta Sankalp, Narang Raj K, Budhiraja Ramji D
Nanomedicine Research Centre, Department of Pharmaceutics, I.S.F. College of Pharmacy, Moga-142001 (Punjab), India.
Sci Pharm. 2011 Jul-Sep;79(3):673-94. doi: 10.3797/scipharm.1011-05. Epub 2011 May 19.
The present study has been undertaken to apply the concept of nanoparticulate mucopenetrating drug delivery system for complete eradication of Helicobacter pylori (H. pylori), colonised deep into the gastric mucosal lining. Most of the existing drug delivery systems have failed on account of either improper mucoadhesion or mucopenetration and no dosage form with dual activity of adhesion and penetration has been designed till date for treating H. pylori induced disorders. In the present study, novel chitosan-alginate polyelectrolyte complex (CS-ALG PEC) nanoparticles of amoxicillin have been designed and optimized for various variables such as pH and mixing ratio of polymers, concentrations of polymers, drug and surfactant, using 3(3) Box-Behnken design. Various studies like particle size, surface charge, percent drug entrapment, in-vitro mucoadhesion and in-vivo mucopenetration of nanoparticles on rat models were conducted. The optimised FITC labelled CS-ALG PEC nanoparticles have shown comparative low in-vitro mucoadhesion with respect to plain chitosan nanoparticles, but excellent mucopenetration and localization as observed with increased fluorescence in gastric mucosa continuously over 6 hours, which clinically can help in eradication of H. pylori.
本研究旨在应用纳米颗粒黏液穿透药物递送系统的概念,以彻底根除深入定植于胃黏膜内层的幽门螺杆菌(H. pylori)。大多数现有的药物递送系统由于黏膜黏附不当或黏液穿透不足而失败,迄今为止尚未设计出具有黏附与穿透双重活性的剂型来治疗幽门螺杆菌引起的疾病。在本研究中,采用三水平三因素的Box-Behnken设计,针对pH值、聚合物混合比例、聚合物浓度、药物浓度和表面活性剂浓度等变量,设计并优化了阿莫西林的新型壳聚糖-海藻酸盐聚电解质复合物(CS-ALG PEC)纳米颗粒。对纳米颗粒进行了粒径、表面电荷、药物包封率、体外黏膜黏附以及在大鼠模型上的体内黏液穿透等各项研究。优化后的异硫氰酸荧光素(FITC)标记的CS-ALG PEC纳米颗粒与普通壳聚糖纳米颗粒相比,体外黏膜黏附性较低,但具有出色的黏液穿透和定位能力,在6小时内胃黏膜中的荧光持续增强,这在临床上有助于根除幽门螺杆菌。