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Eudragit S100 Coated Citrus Pectin Nanoparticles for Colon Targeting of 5-Fluorouracil

机译:Eudragit S100包覆的柑橘果胶纳米颗粒用于5-氟尿嘧啶结肠靶向治疗

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摘要

In the present study, Eudragit S100 coated Citrus Pectin Nanoparticles (E-CPNs) were prepared for the colon targeting of 5-Fluorouracil (5-FU). Citrus pectin also acts as a ligand for galectin-3 receptors that are over expressed on colorectal cancer cells. Nanoparticles (CPNs and E-CPNs) were characterized for various physical parameters such as particle size, size distribution, and shape etc. In vitro drug release studies revealed selective drug release in the colonic region in the case of E-CPNs of more than 70% after 24 h. In vitro cytoxicity assay (Sulphorhodamine B assay) was performed against HT-29 cancer cells and exhibited 1.5 fold greater cytotoxicity potential of nanoparticles compared to 5-FU solution. In vivo data clearly depicted that Eudragit S100 successfully guarded nanoparticles to reach the colonic region wherein nanoparticles were taken up and showed drug release for an extended period of time. Therefore, a multifaceted strategy is introduced here in terms of receptor mediated uptake and pH-dependent release using E-CPNs for effective chemotherapy of colorectal cancer with uncompromised safety and efficacy.
机译:在本研究中,制备了Eudragit S100包衣的柑橘果胶纳米颗粒(E-CPNs),用于结肠靶向5-氟尿嘧啶(5-FU)。柑橘果胶还充当在结肠直肠癌细胞上过度表达的Galectin-3受体的配体。表征了纳米粒子(CPN和E-CPN)的各种物理参数,例如粒径,尺寸分布和形状等。体外药物释放研究表明,在E-CPN大于70的情况下,结肠区域选择性释放药物24小时后,%。针对HT-29癌细胞进行了体外细胞毒性试验(磺胺多巴胺B试验),与5-FU溶液相比,纳米颗粒的细胞毒性潜力高1.5倍。体内数据清楚地表明,Eudragit S100成功地保护了纳米颗粒,使其到达结肠区域,纳米颗粒被吸收并显示出较长时间的药物释放。因此,就受体介导的摄取和使用E-CPNs进行pH依赖性释放而言,本文引入了一种多方面的策略,可有效地对结直肠癌进行化学疗法,且安全性和有效性不受影响。

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