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An Orally Administrated Hyaluronan Functionalized Polymeric Hybrid Nanoparticle System for Colon-Specific Drug Delivery

机译:口服给药的透明质酸功能化的聚合物杂化纳米粒子系统的结肠特定的药物输送。

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摘要

There is a pressing clinical need for advanced colon-specific local drug delivery systems that can provide major advantages in treating diseases associated with the colon, such as inflammatory bowel disease (IBD) and colon cancer. A precise colon targeted drug delivery platform is expected to reduce drug side effects and increase the therapeutic response at the intended disease site locally. In this study, we report the fabrication of hyaluronan (HA) functionalized polymeric hybrid nanoparticulate system (Cur-HA NPs) by using curcumin as a model fluorescent drug. The Cur-HA NPs were about 200–300 nm in size, −51.3 mV overall surface charge after HA functionalization, with 56.0% drug released after 72 h in simulated gastrointestinal fluids. The Cur-HA NPs did not exhibit any cytotoxicity by AlamarBlue, PicoGreen and Live/Dead assays. Following the Cur-HA NPs use on HT-29 monolayer cell cultures demonstrating, the efficacy of HA functionalization increases cellular interaction, uptake when compared to uncoated nanoparticulate system. These findings indicate that HA functionalized nano-hybrid particles are effective in delivering drugs orally to the lower gastrointestinal tract (GIT) in order to treat local colonic diseases.
机译:迫切需要先进的结肠特异性局部药物递送系统,该系统可在治疗与结肠相关的疾病(例如炎症性肠病(IBD)和结肠癌)方面提供主要优势。预期精确的结肠靶向药物递送平台可减少药物副作用并提高局部预期疾病部位的治疗反应。在这项研究中,我们报告了使用姜黄素作为模型荧光药物制备透明质酸(HA)功能化的聚合物杂化纳米颗粒系统(Cur-HA NPs)。在HA功能化后,Cur-HA NP的大小约为200-300 nm,总表面电荷为-51.3 mV,72 h后在模拟胃肠液中释放出56.0%的药物。通过AlamarBlue,PicoGreen和Live / Dead分析,Cur-HA NPs没有表现出任何细胞毒性。在证明Cur-HA NPs用于HT-29单层细胞培养物中后,与未包被的纳米颗粒系统相比,HA功能化的功效增加了细胞相互作用和摄取。这些发现表明,HA功能化的纳米杂化颗粒可有效地将药物口服递送至下胃肠道(GIT),以治疗局部结肠疾病。

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