Department of Pharmaceutical Technology, Gazi University Faculty of Pharmacy, 06330, Ankara, Turkey.
Department of Pharmacology and Toxicology, Ankara University Faculty of Veterinary Medicine, 06110, Ankara, Turkey.
J Pharm Sci. 2018 May;107(5):1398-1407. doi: 10.1016/j.xphs.2018.01.006. Epub 2018 Jan 12.
Nanoparticulate systems have been receiving a significant attention especially for the treatment of cancer but one of the main hurdles is to produce these developed and high-tech nanosystems in large quantities. Anticancer drug formulations are generally designed for parenteral administrations but oral administration is still the most convenient route. In this study, orally applicable nano-sized chitosan nanoparticles (NPs) were successfully prepared using Nano Spray Dryer. It is possible to produce these NPs in large quantities by simply increasing the processing time using the machine without changing any parameter. A chemotherapeutic agent (imatinib mesylate; IMA) and nonsteroidal anti-inflammatory drug (dexketoprofen trometamol) were loaded together in these NPs. NPs were also functionalized with polyethylene glycol and folic acid to obtain long circulating NPs and tumor targeting. The antitumoral activities of formulations showed that these developed NPs can enhance the effectiveness. Animal experiments were performed on fibrosarcoma-bearing mice model, and the treatment with 0.8 mg/μL/kg IMA-loaded chitosan NPs was found to be successful to slow down the growth of tumors. The tumor tissues were removed from the animals and enzymatic activities were evaluated. The inhibitory effect of tyrosine kinase was found to be enhanced from 36.4% to 68.4% when IMA was used in combination with dexketoprofen trometamol. Furthermore, all dried NPs were found to be stable for more than a year at 25°C. Presented results show that these developed combinatorial drug-loaded NPs can be used for the treatment of fibrosarcoma, and these data can provide an insight, new strategies for productions or alternatives in cancer treatment.
纳米颗粒系统受到了极大的关注,特别是在癌症治疗方面,但主要的障碍之一是如何大量生产这些先进的高科技纳米系统。抗癌药物制剂通常设计用于注射给药,但口服给药仍然是最方便的途径。在这项研究中,成功地使用纳米喷雾干燥器制备了可口服的纳米级壳聚糖纳米颗粒(NPs)。通过简单地增加机器的处理时间而不改变任何参数,就可以大量生产这些 NPs。将化疗药物(甲磺酸伊马替尼;IMA)和非甾体抗炎药(右旋酮洛芬氨丁三醇)一起负载到这些 NPs 中。还对 NPs 进行了聚乙二醇和叶酸的功能化,以获得长循环 NPs 和肿瘤靶向。制剂的抗肿瘤活性表明,这些开发的 NPs 可以提高疗效。在纤维肉瘤荷瘤小鼠模型上进行了动物实验,发现用 0.8mg/μL/kg 的载 IMA 壳聚糖 NPs 治疗可以成功减缓肿瘤的生长。从动物中取出肿瘤组织并评估酶活性。当 IMA 与右旋酮洛芬氨丁三醇联合使用时,发现酪氨酸激酶的抑制作用从 36.4%增强到 68.4%。此外,所有干燥的 NPs 在 25°C 下稳定保存超过一年。目前的结果表明,这些开发的组合药物负载 NPs 可用于治疗纤维肉瘤,这些数据可为癌症治疗提供新的见解、新的生产策略或替代方案。