Drug Microbiology Lab, Drug Radiation Research Department, Biotechnology Division, National Center for Radiation Research and Technology (NCRRT), Atomic Energy Authority, Cairo, Egypt.
Drug Microbiology Lab, Drug Radiation Research Department, Biotechnology Division, National Center for Radiation Research and Technology (NCRRT), Atomic Energy Authority, Cairo, Egypt.
Int J Biol Macromol. 2020 Aug 1;156:1584-1599. doi: 10.1016/j.ijbiomac.2019.11.210. Epub 2019 Nov 29.
The novelty of the present work looks in the synthesis of aqueous dispersed selenium nanoparticles (Se NPs) using gamma rays with the aid of various natural macromolecules such as citrus pectin (CP), sodium alginate (Alg), chitosan (CS) and aqueous extract of fermented fenugreek powder (AEFFP) using Pleurotus ostreatus for investigating their impact in vitro toward carcinoma cell. The synthesized Se NPs were characterized by XRD, UV-Vis., DLS, HRTEM, SEM, EDX and FTIR. Nucleation and growth mechanisms were also discussed. The factorial design was applied to examine the importance of multiple parameters on Se NPs production with a special focus on temperature and gamma rays influences. FTIR spectrum exhibited the existence of several functional groups in Se NPs-capping macromolecules. Results revealed that Se NPs' size was dramatically-influenced by the type of stabilizer, precursors concentration, pH and the absorbed gamma rays dose. The current research reported the promising antitumor application of Se NPs against Ehrlich Ascites Carcinoma (EAC) and human Colon Adenocarcinoma (CACO) in vitro. The proliferation of EAC was significantly-hindered by Se NPs-CS (38.0 μg/ml) at 60 kGy (IC = 23.12%) and Se NPs-AEFFP (19.00 μg/ml) at 15 kGy (IC = 7.21%). Also, Se NPs control the generation of CACO cells, IC was recorded as 25.32% for Se NPs-CS (38.0 μg/ml) and 8.57% for Se NPs-AEFFP (19.00 μg/ml).
本工作的新颖之处在于使用γ射线辅助各种天然大分子(如柑橘果胶(CP)、海藻酸钠(Alg)、壳聚糖(CS)和发酵胡芦巴粉的水提物(AEFFP))合成水相分散硒纳米粒子(Se NPs),使用糙皮侧耳( Pleurotus ostreatus)研究其对癌细胞的体外影响。所合成的 Se NPs 通过 XRD、UV-Vis、DLS、HRTEM、SEM、EDX 和 FTIR 进行了表征。还讨论了成核和生长机制。应用析因设计来检查多个参数对 Se NPs 生产的重要性,特别关注温度和γ射线的影响。FTIR 光谱表明 Se NPs-封端大分子中存在几个官能团。结果表明,Se NPs 的尺寸受稳定剂类型、前体浓度、pH 值和吸收的 γ 射线剂量的显著影响。目前的研究报道了 Se NPs 对艾氏腹水癌(EAC)和人结肠腺癌(CACO)的体外抗肿瘤应用的前景。Se NPs-CS(38.0μg/ml)在 60kGy 时(IC=23.12%)和 Se NPs-AEFFP(19.00μg/ml)在 15kGy 时(IC=7.21%)显著抑制了 EAC 的增殖。此外,Se NPs 控制 CACO 细胞的产生,Se NPs-CS(38.0μg/ml)的 IC 为 25.32%,Se NPs-AEFFP(19.00μg/ml)的 IC 为 8.57%。