天然产物研究与开发 ›› 2023, Vol. 35 ›› Issue (12): 2117-2126.doi: 10.16333/j.1001-6880.2023.12.011

• 开发研究 • 上一篇    下一篇

岩藻多糖纳米硒的制备及其抑制肿瘤细胞增殖的研究

陈博文1,陈建平1,2*,黄文浩1,钟赛意1,2,李瑞1,2,宋兵兵1,2,刘晓菲1,2,汪  卓1,2   

  1. 1广东海洋大学食品科技学院 广东省水产品加工与安全重点实验室,湛江 524088;
    2大连工业大学海洋食品精深加工关键技术省部共建协同创新中心,大连 116034
  • 出版日期:2023-12-28 发布日期:2023-12-27
  • 基金资助:
    广东省自然科学基金面上项目(2021A1515012455);湛江市科技计划(2022A01045);广东海洋大学“南海学者计划”(0020 29002009);广东省普通高校创新团队项目(2021KCXTD021)

Preparation of selenium nanoparticles decorated by fucoidan and its inhibition effect on tumor cells growth

CHEN Bo-wen1,CHEN Jian-ping1,2*,HUANG Wen-hao1,ZHONG Sai-yi1,2,LI Rui1,2,SONG Bing-bing1,2,LIU Xiao-fei1,2,WANG Zhuo1,2   

  1. 1College of Food Science and Technology,Guangdong Ocean University,Guangdong Provincial Key Laboratory of Aquatic Product Processing and Safety,Zhanjiang 524088,China;2Dalian Polytechnic University,Collaborative Innovation Center of Seafood Deep Processing,Dalian 116034,China
  • Online:2023-12-28 Published:2023-12-27

摘要: 探索岩藻多糖纳米硒(fucoidan-selenium nanoparticles,FD-SeNPs)的制备工艺条件,并进一步对其进行结构表征和抑制肿瘤细胞增殖的研究。以岩藻多糖(fucoidan,FD)为模板,采用抗坏血酸(ascorbic acid,Vc)还原亚硒酸钠(Na2SeO3)制备FD-SeNPs,通过单因素和响应面实验优化其工艺参数。采用傅里叶变换红外光谱仪(FT-IR)、扫描电子显微镜(SEM)、能量色散X射线谱仪(EDX)、透射电子显微镜(TEM)和X射线衍射仪(XRD)对其进行结构表征;运用MTT法测定其对HepG2肝癌细胞和A549肺癌细胞存活率的影响。结果表明,FD-SeNPs的最佳制备工艺参数为:反应时间为1 h、反应温度为35 ℃、抗坏血酸与亚硒酸钠的摩尔比为14∶1、FD浓度为0.8 mg/mL,在此条件下制备得到的FD-SeNPs粒径为(83.40 ± 0.55)nm、电位为(-31.89 ± 0.47)mV、含硒量达29.93%。经鉴定,FD-SeNPs的表面形貌为均一的球形,由77.59% Se、17.70% C和3.41% O元素组成。MTT实验结果表明,FD-SeNPs能显著抑制HepG2肝癌细胞和A549肺癌细胞的增殖,具有良好的剂量效应。上述结果表明,已成功制备FD-SeNPs并表现出一定的抑制肿瘤细胞增殖的能力,为其在抗肿瘤临床药物的应用开发提供了一定的技术手段和理论数据参考。

关键词: 岩藻多糖, 纳米硒, 结构表征, 抑制肿瘤细胞增殖

Abstract: This study were to explore the preparation technology conditions of fucoidan-selenium nanoparticles (FD-SeNPs),and to further characterize their structure and investigate their inhibition effects on tumor cells growth.Using fucoidan (FD) as a template,ascorbic acid (Vc) was used to reduce sodium selenite (Na2SeO3) to prepare FD-SeNPs,and the process parameters were optimized by single factor design and response surface experiments.Fourier transform infrared spectrometer (FT-IR),scanning electron microscope (SEM),energy dispersive X-ray spectroscopy (EDX),transmission electron microscope (TEM) and X-ray diffraction (XRD) were used to characterize its structure.The MTT method was used to determine its effect on the survival rates of HepG2 hepatoma cells and A549 lung cancer cells.The results showed that the optimal conditions of FD-SeNPs were list as follows:the reaction time of 1 h,the reaction temperature of 35 ℃,molar ratio of Vc to Na2SeO3 of 14∶1,and FD concentration of 0.8 mg/mL.Under these conditions,the FD-SeNPs with particle size of (83.4 ± 0.55) nm,Zeta potential of (-31.89 ± 0.47) mV and selenium content of 29.93 % was obtained.After identification,its surface morphology was uniform spherical,which was composed of 77.59% Se,17.70% C and 3.41% O elements.The results of MTT assay showed that FD-SeNPs could significantly inhibited the proliferation of HepG2 cells and A549 lung cancer cells,and had a good dose effect.The above results showed that the FD-SeNPs had been successfully prepared and exhibited certain inhibitory effects on tumor cells growth,which provided a certain technical means and theoretical data reference for the application and development of anti-tumor clinical drugs.

Key words: fucoidan, selenium nanoparticles, structural identification, inhibition effect on tumor cells growth

中图分类号:  R735.7