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色甘酸壳聚糖纳米颗粒作为一种新型的结直肠癌保护方法。

Cromolyn chitosan nanoparticles as a novel protective approach for colorectal cancer.

作者信息

Motawi Tarek K, El-Maraghy Shohda A, ElMeshad Aliaa Nabil, Nady Omnia M, Hammam Olfat A

机构信息

Biochemistry Department, Faculty of Pharmacy, Cairo University, Kasr El Ainy st., Cairo 11562, Egypt.

Pharmaceutics and Industrial Pharmacy Department, Faculty of Pharmacy, Cairo University, Kasr El Ainy st., Cairo 11562, Egypt.

出版信息

Chem Biol Interact. 2017 Sep 25;275:1-12. doi: 10.1016/j.cbi.2017.07.013. Epub 2017 Jul 18.

Abstract

Colorectal cancer is the third most common cancer in the world. Cromolyn is a mast cell stabilizer and was proposed as an anticancer agent; however its high polarity limits its bioavailability by rapid washing from the body. We formulated 10 cromolyn chitosan nanoparticles (CCSNPs) following ionic gelation technique to improve its bioavailability and investigated the protective anticancer effect of the optimum formula against colorectal cancer in dimethylhydrazine-induced model in rats. Rats were divided into seven groups, group-1: normal control, group-2: cromolyn control, group-3: CCSNPs control, groups-4 to 7 received dimethylhydrazine for 16 weeks to induce colorectal cancer. Groups-5 to 7 received cromolyn solution, non-medicated chitosan nanoparticles and CCSNPs, respectively as protective treatments. Optimum CCSNPs (size 112.4 nm, charge +39.9 mV, enclosed 93.6% cromolyn and showed a sustained drug release pattern over 48 h) significantly reduced tumor-signaling molecules and the number of aberrant crypt foci compared to dimethylhydrazine. Histopathological examination of colon samples revealed that CCSNPs exerted an augmented protective anticancer effect by ameliorating tumor pathology compared to cromolyn solution. In conclusion, CCSNPs ameliorated tumor pathology and malignant oncogenic signaling molecules in colorectal cancer tissue. Thus, CCSNPs may provide a novel protective approach in colorectal cancer treatment. Moreover, encapsulating cromolyn in chitosan nanoparticles augmented the protective anticancer effect of the drug.

摘要

结直肠癌是全球第三大常见癌症。色甘酸是一种肥大细胞稳定剂,曾被提议作为抗癌剂;然而,其高极性导致它在体内迅速被清除,限制了其生物利用度。我们采用离子凝胶技术制备了10种色甘酸壳聚糖纳米粒(CCSNPs)以提高其生物利用度,并在二甲基肼诱导的大鼠结直肠癌模型中研究了最佳配方对结直肠癌的保护性抗癌作用。大鼠被分为七组,第一组:正常对照组;第二组:色甘酸对照组;第三组:CCSNPs对照组;第四至七组接受二甲基肼处理16周以诱导结直肠癌。第五至七组分别接受色甘酸溶液、未载药的壳聚糖纳米粒和CCSNPs作为保护性治疗。最佳CCSNPs(粒径112.4 nm,电荷+39.9 mV,包封率93.6%,并在48小时内呈现药物缓释模式)与二甲基肼组相比,显著降低了肿瘤信号分子和异常隐窝病灶的数量。结肠样本的组织病理学检查显示,与色甘酸溶液相比,CCSNPs通过改善肿瘤病理学表现发挥了增强的保护性抗癌作用。总之,CCSNPs改善了结直肠癌组织的肿瘤病理学和恶性致癌信号分子。因此,CCSNPs可能为结直肠癌治疗提供一种新的保护方法。此外,将色甘酸包裹在壳聚糖纳米粒中增强了该药物的保护性抗癌作用。

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