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
作 者:贺茂芳 张博[1] 唐一梅[1] 韩禄[1] HE Mao-Fang;ZHANG Bo;TANG Yi-Mei;HAN Lu(College of Pharmacy,Institute of Drug Research,Xi′an Medical University,Xi′an 710021,China)
机构地区:[1]西安医学院药学院,西安医学院药物研究所,西安710021
出 处:《分析化学》2018年第9期1486-1492,共7页Chinese Journal of Analytical Chemistry
基 金:本文系西安医学院博士科研启动基金(No.2016D0C06)和国家自然科学基金孵育项目(No.2017 GJFU08)资助。
摘 要:为了获得高容量的阴离子交换吸附剂,本研究以Fe_3O_4磁性纳米粒子为基质,在其表面包覆聚多巴胺,然后与树枝状大分子聚乙烯亚胺反应,制得多氨基化磁性微球。此微球的离子交换容量为9.1 mmol/g。采用透射电镜、红外光谱和热重分析对材料进行了表征。以β-酪蛋白和牛血清蛋白(BSA)为模型蛋白,采用静态吸附法研究了此微球对蛋白质的吸附性能,在最佳条件下测定了微球对蛋白质的静态吸附等温线。结果表明,此微球对蛋白质的最佳吸附时间为2h,缓冲溶液的最佳pH值为7.0。在此条件下,对β-酪蛋白和BSA的最大吸附容量分别为237.5和204.5μg/mg,而对溶菌酶和核糖核酸酶A几乎不产生吸附。实验结果表明,此微球对酸性蛋白具有选择性,在蛋白质分离纯化方面具有良好的应用前景。A high capacity anion exchange magnetic absorbent was prepared by immobilization of hyperbranched polyethyleneimine(PEI)on polydopamine-coated Fe 3O 4 microspheres(Fe 3O 4@pDA)and the ion exchange capacity was determined as 9.1 mmol/g.The absorbent was characterized by transmission electron microscope(TEM),infrared spectroscopy(IR)and thermogravimetric analysis(TGA).Moreover,the adsorption behavior of the absorbent for protein was carefully investigated by static adsorption using bovine serum albumin(BSA)andβ-casein as models and then the static isotherms were determined under the optimum conditions.It was shown that the highest adsorption amount for protein was obtained when the adsorption time was 2 h and the pH was 7.0.Under the optimum conditions,the saturated adsorption capacity towardsβ-casein and BSA was determined as high as 237.5 and 204.5μg/mg,respectively.Comparatively,the adsorbent exhibited little adsorption towards lysozyme and Rnase A,showing highly selectivity towards acidic protein.Therefore,the adsorbent exhibited potential in the separation and purification of protein from real samples.
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:216.73.216.200