检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
机构地区:[1]军事医学科学院卫生学环境医学研究所,天津市环境与食品安全风险监控技术重点实验室,天津300050 [2]河北科技大学环境科学与工程学院
出 处:《解放军预防医学杂志》2017年第1期1-5,共5页Journal of Preventive Medicine of Chinese People's Liberation Army
基 金:国家自然科学基金资助项目(No.21207161)
摘 要:目的用化学共沉淀法制备了四氧化三铁(Fe_3O_4)磁性纳米颗粒并进行氨基修饰和定量。方法分别采用"将磁颗粒包覆硅壳后修饰氨基"和"直接修饰氨基"两种不同方法对磁性纳米颗粒的表面进行氨基修饰,并通过对硝基苯甲醛比色法对表面氨基进行定量,比较两种方法的修饰效果。通过透射电子显微镜(TEM)、傅立叶变换红外光谱仪(FTIR)、震动样品磁强计(VSM)对其进行表征。结果所合成的颗粒粒径比较均一,包覆的硅壳在6 nm左右,且具有超顺磁性,在外加磁场作用下能够实现快速有效的分离。氨基定量结果显示有硅壳包覆的磁颗粒的氨基量明显多于3-氨基丙基三乙氧基硅烷(APTES)直接修饰磁颗粒的氨基量。结论有硅壳包覆的磁性纳米颗粒更适合进行下一步的生物功能化修饰,能够适应更广泛的生物应用。Objective To obtain Fe304 magnetic nanoparticles by chemical co-precipitation method and modifiy them by amino groups which have been quantified. Methods Two different amino-modified Fe304 magnetic nanoparticles were obtained using two different modification methods: amino-modification after nanoparticles are coated by silicon and direct amino-modification respectively. The nanoparticles were characterized by transmission electron microscopy (TEM), Fourier transform infrared spectroscopy ( FTIR), and vibration sample magnetic machine (VSM). The amount of amino group modified on the surface was determined by colorimetric method that involved amino reacting with p-nitrobenzaldehyde. Results The TEM results indicated that the particle size was relatively uniform and the silica shell was about 6nm. Moreover, the magnetic nanoparticles were superparamagnetic and could be separated in a magnetic field quickly and effectively. We compared the two methods and the results showed there was much more amine on the surface of Fe3O4 coated by silica than that by direct amino-modification. Conclusion The magnetic nanoparticles coated with silicon shell are more suitable for the next step of biological functional modification and can be used in a wider range of biological applications.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.222