Hudiță Ariana, Radu Ionuț Cristian, Zaharia Cătălin, Ion Andreea Cristina, Ginghină Octav, Gălățeanu Bianca, Măruțescu Luminița, Grama Florin, Tsatsakis Aristidis, Gurevich Leonid, Costache Marieta
Department of Biochemistry and Molecular Biology, University of Bucharest, 91-95 Splaiul Independentei Street, 050095 Bucharest, Romania.
Advanced Polymer Materials Group, University Politehnica of Bucharest, 1-7 Gh. Polizu Street, 011061 Bucharest, Romania.
Pharmaceutics. 2021 May 19;13(5):755. doi: 10.3390/pharmaceutics13050755.
5-fluorouracil (5-FU) remains the gold standard of treatment for colorectal cancer, but its poor bioavailability and high systemic toxicity highlight the urgent need for the development of novel delivery strategies to increase the efficacy of 5-FU treatment. The present study is aimed to design and validate a PEGylated Silk Fibroin Nanocarrier (SF/PEG nanoparticles (NPs)) as an efficient 5-FU delivery system for potential intravenous administration. Using the human adenocarcinoma HT-29 cell line as an in vitro model for colorectal cancer, the cytotoxicity screening of the SF/PEG NPs showed that pristine nanocarriers were highly biocompatible, while the addition of 5-FU triggers a dramatic reduction in tumor cell viability, proliferation potential and mitochondrial integrity as well as a significant increase in nitric oxide production. Despite their high in vitro cytotoxicity, the 5-FU SF/PEG NPs were found hemocompatible as no impact on red blood cells hemolysis or the phagocytic activity of the granulocytes was observed. Exposure of HT-29 tumor cells and blood samples to 5-FU SF/PEG NPs augmented the tumor necrosis factor-α levels. Moreover, 5-FU SF/PEG NPs showed an impact on tumor cell migration and invasive potential as both of these processes were inhibited by the NP treatment.
5-氟尿嘧啶(5-FU)仍然是结直肠癌治疗的金标准,但其生物利用度低和全身毒性高凸显了迫切需要开发新的递送策略以提高5-FU治疗效果。本研究旨在设计并验证一种聚乙二醇化丝素蛋白纳米载体(SF/PEG纳米颗粒(NPs))作为一种高效的5-FU递送系统,用于潜在的静脉给药。以人腺癌HT-29细胞系作为结直肠癌的体外模型,SF/PEG NPs的细胞毒性筛选表明,原始纳米载体具有高度生物相容性,而添加5-FU会导致肿瘤细胞活力、增殖潜能和线粒体完整性显著降低,同时一氧化氮生成显著增加。尽管5-FU SF/PEG NPs在体外具有高细胞毒性,但发现其具有血液相容性,因为未观察到对红细胞溶血或粒细胞吞噬活性有影响。将HT-29肿瘤细胞和血液样本暴露于5-FU SF/PEG NPs会增加肿瘤坏死因子-α水平。此外,5-FU SF/PEG NPs对肿瘤细胞迁移和侵袭潜能有影响,因为NP处理抑制了这两个过程。