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用于靶向药物递送至炎症结肠的酶/ pH双敏感聚合物纳米颗粒。

Enzyme/pH dual sensitive polymeric nanoparticles for targeted drug delivery to the inflamed colon.

作者信息

Naeem Muhammad, Kim Wooseong, Cao Jiafu, Jung Yunjin, Yoo Jin-Wook

机构信息

College of Pharmacy, Pusan National University, Busan 609-735, South Korea.

College of Pharmacy, Pusan National University, Busan 609-735, South Korea.

出版信息

Colloids Surf B Biointerfaces. 2014 Nov 1;123:271-8. doi: 10.1016/j.colsurfb.2014.09.026. Epub 2014 Sep 20.

Abstract

Novel nanoparticles whose drug release profiles are controlled by both enzyme and pH were prepared for the colon-specific drug delivery using a polymeric mixture of enzyme-sensitive azo-polyurethane and pH-sensitive Eudragit S100 (ES-Azo.pu). The enzyme/pH dual sensitive nanoparticles were designed to release a drug based on a two-fold approach which specifically aimed to target drug delivery to the inflamed colon while preventing the burst release of drugs in the stomach and small intestine. Single pH-sensitive (ES) and dual sensitive (ES-Azo.pu) nanoparticles were prepared using an oil-in-water emulsion solvent evaporation method and coumarin-6 (C-6) was used as a model drug. The successful formation of ES and ES-azo.pu nanoparticles that have 214 nm and 244 nm in mean particle size, respectively, was confirmed by scanning electron microscopy and qNano. ES nanoparticles showed almost 100% of burst drug release at pH 7.4, whereas ES-Azo.pu nanoparticles prevented the burst drug release at pH 7.4, followed by a sustained release phase thereafter. Furthermore, ES-Azo.pu nanoparticles exhibited enzyme-triggered drug release in the presence of rat cecal contents obtained from a rat model of colitis. An in vivo localization study in rat gastrointestinal tract demonstrated that ES-Azo.pu nanoparticles were selectively distributed in the inflamed colon, showing 5.5-fold higher C-6 than ES nanoparticles. In conclusion, the enzyme/pH dual sensitive nanoparticles presented in this study can serve as a promising strategy for colon-specific drug delivery against inflammatory bowel disease and other colon disorders.

摘要

使用酶敏感的偶氮聚氨酯和pH敏感的Eudragit S100(ES-Azo.pu)的聚合物混合物,制备了药物释放曲线受酶和pH共同控制的新型纳米颗粒,用于结肠特异性药物递送。酶/pH双敏感纳米颗粒的设计基于双重方法来释放药物,该方法专门旨在将药物靶向递送至发炎的结肠,同时防止药物在胃和小肠中突发释放。使用水包油乳液溶剂蒸发法制备了单pH敏感(ES)和双敏感(ES-Azo.pu)纳米颗粒,并使用香豆素-6(C-6)作为模型药物。通过扫描电子显微镜和qNano证实成功形成了平均粒径分别为214 nm和244 nm的ES和ES-azo.pu纳米颗粒。ES纳米颗粒在pH 7.4时显示出几乎100%的突发药物释放,而ES-Azo.pu纳米颗粒在pH 7.4时可防止药物突发释放,随后进入持续释放阶段。此外,ES-Azo.pu纳米颗粒在存在从结肠炎大鼠模型获得的大鼠盲肠内容物的情况下表现出酶触发的药物释放。大鼠胃肠道的体内定位研究表明,ES-Azo.pu纳米颗粒选择性地分布在发炎的结肠中,其C-6含量比ES纳米颗粒高5.5倍。总之,本研究中提出的酶/pH双敏感纳米颗粒可作为一种有前景的策略,用于针对炎症性肠病和其他结肠疾病的结肠特异性药物递送。

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