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作 者:刘素素 王文博 李璋龙 陈嘉程 王银川 喻长远[1] 刘佳蕙[2] 王诗卉 LIU SuSu;WANG WenBo;LI ZhangLong;CHEN JiaCheng;WANG YinChuan;YU ChangYuan;LIU JiaHui;WANG ShiHui(College of Life Science and Technology,Beijing University of Chemical Technology,Beijing 100029;Analytical Instrumentation Center,College of Chemistry and Molecular Engineering,Peking University,Beijing 100871,China)
机构地区:[1]北京化工大学生命科学与技术学院,北京100029 [2]北京大学化学与分子工程学院分析测试中心,北京100871
出 处:《北京化工大学学报(自然科学版)》2024年第4期44-50,共7页Journal of Beijing University of Chemical Technology(Natural Science Edition)
基 金:国家自然科学基金(82174531/21606013);国家重点研发计划(218YFA0903000)。
摘 要:以蒲公英提取液为还原剂、氯金酸为原料合成了蒲公英金纳米颗粒(Da-AuNPs),采用多种手段对其进行了表征,结果表明:Da-AuNPs呈球形或近球形,平均粒径约为(21.2±3.0) nm;蒲公英中含丰富羟基的活性物质可能是合成Da-AuNPs的主要还原剂;金纳米颗粒具有典型的面心立方(FCC)晶格结构;Da-AuNPs悬液放置5 d,其粒径没有显著变化,体系具有较好的稳定性。采用噻唑蓝溴化四唑(MTT)试验对Da-AuNPs进行了体外细胞毒性测试,结果显示:在6.25~200μg/mL的范围内,Da-AuNPs对RAW264.7正常细胞具有良好的生物相容性;当Da-AuNPs的质量浓度为200μg/mL时,在808 nm的近红外线(1.5 W/cm^(2))下照射3 min,与对照组相比4T1癌细胞活力下降至65%,表明Da-AuNPs具有一定的体外抗癌活性。Dandelion gold nanoparticles(Da-AuNPs) were synthesized by using dandelion extract as a reducing agent and chloroauric acid as raw material and characterized by various methods. The results show that Da-AuNPs are spherical or nearly spherical, and the average particle size is(21.2±3.0) nm. The active substances containing abundant hydroxyl groups in dandelions may be the main reducing agents for the synthesis of Da-AuNPs. Gold nanoparticles have a typical face-centered cubic(FCC) lattice structure. When a Da-AuNPs suspension was left for 5 days, its particle size did not change significantly, indicating that the system had good stability. The in vitro cytotoxicity of Da-AuNPs was tested by MTT assay. The results showed that Da-AuNPs had good biocompatibility to RAW264.7 normal cells in the range 6.25-200 μg/mL. After exposure to 808 nm near-infrared radiation(1.5 W/cm^(2)) for 3 min, when the mass concentration of Da-AuNPs was 200 μg/mL, the viability of 4T1 cancer cells decreased to 65% compared with the control group, indicating that Da-AuNPs had a certain anti-cancer activity in vitro.
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