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利用明胶纳米载体递送至肺部治疗肺癌的甲氨蝶呤。

Exploiting gelatin nanocarriers in the pulmonary delivery of methotrexate for lung cancer therapy.

机构信息

Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Ain Shams University, Cairo, Egypt; School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Liverpool, United Kingdom.

Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Ain Shams University, Cairo, Egypt.

出版信息

Eur J Pharm Sci. 2019 May 15;133:115-126. doi: 10.1016/j.ejps.2019.03.016. Epub 2019 Mar 21.

Abstract

Gelatin has many merits that encourage its use in the pulmonary delivery of anticancer drugs. It is a biodegradable denatured protein which possesses several functional groups that could be modified. Additionally, it has balanced hydrophilic and hydrophobic characters, which facilitate the loading of chemotherapeutic agents. Accordingly, the purpose of the current work was to exploit this valuable biomaterial in the efficient pulmonary delivery of methotrexate in case of lung cancer. Gelatin nanoparticles were prepared via a desolvation method and the fabrication process was optimized using Box Behnken design of experiment. A comparative study on uptake of gelatin nanoparticles by lung adenocarcinoma cells and macrophages was implemented using flow cytometry. Investigation of the effect of different methotrexate loading techniques: encapsulation, post loading and chemical conjugation on the nanoparticles characteristics and cellular cytotoxicity was performed. Nano-in-microparticles were prepared by co-spray drying optimized nanoparticles with leucine. Results showed that Box Behnken design was able to optimize preparation parameters to yield uniform nanoparticles with suitable particle size for cancer cells uptake. The prepared nanoparticles demonstrated a preferential uptake by lung cancer cells. Additionally, methotrexate loaded nanoparticles demonstrated up to four fold significant reduction in methotrexate IC. The spray dried gelatin nano-in microparticles demonstrated good aerosolization properties enabling lung deposition in the respirable airways. Thus, providing a promising platform for lung cancer therapy.

摘要

明胶具有许多优点,鼓励其在抗癌药物的肺部给药中使用。它是一种可生物降解的变性蛋白质,具有多个可修饰的功能基团。此外,它具有平衡的亲水性和疏水性特征,有利于化疗药物的负载。因此,本工作的目的是利用这种有价值的生物材料,在肺癌的情况下,有效地将甲氨蝶呤肺部给药。通过去溶剂化法制备明胶纳米粒,并使用 Box-Behnken 实验设计优化制备工艺。使用流式细胞术对肺腺癌细胞和巨噬细胞对明胶纳米粒的摄取进行了比较研究。考察了不同的甲氨蝶呤载药技术:包封、后载药和化学偶联对纳米粒特性和细胞毒性的影响。采用共喷雾干燥法将优化后的纳米粒与亮氨酸制成纳米-微球。结果表明,Box-Behnken 设计能够优化制备参数,得到适合癌细胞摄取的粒径均匀的纳米粒。所制备的纳米粒表现出对肺癌细胞的优先摄取。此外,载有甲氨蝶呤的纳米粒使甲氨蝶呤的 IC 降低了四倍。喷雾干燥的明胶纳米-微球表现出良好的气溶胶化性能,能够在可吸入气道中沉积于肺部。因此,为肺癌治疗提供了一个有前途的平台。

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