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Development and characterization of pellets for targeted delivery of 5-fluorouracil and phytic acid for treatment of colon cancer in Wistar rat

机译:开发和表征用于靶向递送5-氟尿嘧啶和植酸的小丸用于治疗Wistar大鼠结肠癌

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摘要

The present study was designed to investigate the therapeutic efficacy of metal chelator and anticancer drug in the treatment of colorectal cancer (CRC). Pellets containing Phytic acid, 5- Fluorouracil (5-FU), Microcrystalline cellulose (MCC) PH 101, Hydroxypropyl Methylcellulose (HPMC) and Barium sulfate were prepared by using extrusion spheronization technique. Prepared pellets were coated with Eudragit S100 to achieve colon-specific drug delivery. Pellets were characterized for various pharmaceutical and micromeritic attributes. The in vivo therapeutic efficacy comprising of both pharmacokinetic and pharmacodynamic parameters was determined in Ehrlich ascites carcinoma (EAC) induced cancer animal model. Phytic acid and 5-FU combinations seem to exert higher cytotoxic activity via increased reactive oxygen species (ROS) level by chelating manganese. Further pharmacokinetic studies reveled approximately 50% lower C in the finished formulation, indicates lower systemic exposure to the drug. X-ray radiography ensures the localized delivery of the encapsulated drug. Histopathological studies indicated no significant local toxicity compared to the uncoated formulation. Results inferred that the proposed combination has superior anticancer activity with minimum systemic and local toxicity and it opens a new avenue in the treatment of colorectal cancer.
机译:本研究旨在研究金属螯合剂和抗癌药在结直肠癌(CRC)中的治疗效果。采用挤出滚圆法制备了含植酸,5-氟尿嘧啶(5-FU),微晶纤维素(MCC)PH 101,羟丙基甲基纤维素(HPMC)和硫酸钡的微丸。制备的小丸用Eudragit S100包衣以实现结肠特异性药物递送。粒料具有多种药学和微生特性。在艾氏腹水癌(EAC)诱导的癌症动物模型中确定了包括药代动力学和药效学参数的体内治疗功效。植酸和5-FU的组合似乎通过螯合锰增加了活性氧(ROS)的水平,发挥了更高的细胞毒活性。进一步的药代动力学研究表明最终制剂中的C降低了约50%,表明该药物的全身暴露降低。 X射线射线照相术确保封装药物的局部递送。组织病理学研究表明,与未包衣制剂相比,没有明显的局部毒性。结果表明,所提出的组合具有优异的抗癌活性,同时具有最小的全身和局部毒性,为治疗结直肠癌开辟了新途径。

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