Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmacy, Pharos University in Alexandria, Egypt.
Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmacy, Pharos University in Alexandria, Egypt.
Int J Biol Macromol. 2023 Jun 30;241:124528. doi: 10.1016/j.ijbiomac.2023.124528. Epub 2023 Apr 20.
Fisetin (FS) is an anticancer drug having potential role in oral tumors management. However, its clinical application is limited due to its hydrophobicity and instability. Bioactive polymers-based nanosystems have a great potential in cancer therapy. Herein, different biopolymers were selected for their anticancer activity and targeting ability for nanoparticles preparation namely; fucoidan (FU), zein (Zn) and hyaluronic acid (HA). The selected FS-loaded cross-linked Zn nanoparticles (ZFH) which contains HA& FU for Zn nanoparticles stabilization showed the most suitable particle size (196 ± 6.53 nm), mean surface net charge (-38.8 ± 1.47 mV) and entrapment efficiency (98 ± 1.2 %). This is the first study to utilize both HA &FU not only for stabilization but also for dual targeting effect due to their targeting ability to multiple tumor targets. In-vitro anticancer activity of ZHF revealed remarkable uptake by SCC-4 cells with significant cytotoxic action. Further, ZHF was appraised using 4-nitroquinoline 1-oxide (4-NQO)-induced oral cancer in-vivo; ZHF significantly reduced OSCC-specific serum biomarkers levels, histologic tumor grade and increased caspase-3 level. Moreover, potential of destroying two key tumor regulatory cells; TECs and CSCs, was evaluated using their specific markers. The elaborated ZFH nanoparticles could be considered as promising targeted nanotherapy for oral cancer treatment with enhanced efficacy and survival rate.
非瑟酮(FS)是一种具有口腔肿瘤管理潜力的抗癌药物。然而,由于其疏水性和不稳定性,其临床应用受到限制。基于生物活性聚合物的纳米系统在癌症治疗中具有巨大的潜力。在此,选择了不同的生物聚合物,因其抗癌活性和靶向纳米粒子制备的能力,即褐藻糖胶(FU)、玉米醇溶蛋白(Zn)和透明质酸(HA)。选择的负载 FS 的交联 Zn 纳米颗粒(ZFH)包含用于 Zn 纳米颗粒稳定的 HA 和 FU,其显示出最合适的粒径(196±6.53nm)、平均表面净电荷(-38.8±1.47mV)和包封效率(98±1.2%)。这是首次利用 HA 和 FU 不仅进行稳定化,而且还进行双重靶向作用的研究,因为它们具有针对多种肿瘤靶标的靶向能力。ZHF 的体外抗癌活性显示出对 SCC-4 细胞的显著摄取,具有显著的细胞毒性作用。此外,使用 4-硝基喹啉 1-氧化物(4-NQO)诱导的体内口腔癌评估了 ZHF;ZHF 显著降低了 OSCC 特异性血清生物标志物水平、组织学肿瘤分级和增加了 caspase-3 水平。此外,还评估了其特异性标记物来评估破坏两种关键肿瘤调节细胞(TEC 和 CSC)的潜力。详细阐述的 ZFH 纳米颗粒可被视为用于口腔癌治疗的有前途的靶向纳米疗法,具有增强的疗效和生存率。