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Gold nanoparticles bound on microgel particles and their application as an enzyme support

机译:结合在微凝胶颗粒上的金纳米颗粒及其作为酶载体的应用

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Submicron-sized poly(N-isopropyl acrylamide)/polyethyleneimine core-shell microgels were prepared in aqueous media by using tert-butyl hydroperoxide (TBHP) as an initiator, and then the gold nanoparticles (approx 8 nm) were formed on the surface of the microgels. The amino groups on the polyethyleneimine (PEI) chains act as the binder for the assembly of the gold nanoparticles/microgel complex. In aqueous media the microgels are highly stable with the gold nanoparticles on their extended PEI chains, and this multi-scale nanoparticle complex can be recovered from water and redispersed in water. The nanogold/microgel particles were conjugated with the enzymes horseradish peroxidase (HRP) and urease. It is found that under identical assay conditions the enzymeanogold/microgel systems exhibit enhanced biocatalytic activity over free enzymes in solution, especially at lower enzyme concentrations. In addition, compared to free HRP, the HRPanogold/microgel systems show higher activity at varied pHs and temperatures, as well as higher storage stability. Thus the novel nanogold/microgel particles can serve as an excellent support for enzymes.
机译:以叔丁基过氧化氢(TBHP)为引发剂,在水性介质中制备了亚微米级的聚(N-异丙基丙烯酰胺)/聚乙烯亚胺核壳微凝胶,然后在铜的表面形成金纳米粒子(约8 nm)。微凝胶。聚乙烯亚胺(PEI)链上的氨基充当金纳米颗粒/微凝胶复合物组装的粘合剂。在水性介质中,微凝胶对金纳米颗粒的延长的PEI链高度稳定,这种多尺度的纳米颗粒复合物可以从水中回收并重新分散在水中。将纳米金/微凝胶颗粒与辣根过氧化物酶(HRP)和脲酶结合。发现在相同的测定条件下,酶/纳米金/微凝胶系统相对于溶液中的游离酶表现出增强的生物催化活性,尤其是在较低的酶浓度下。此外,与游离HRP相比,HRP /纳米金/微凝胶系统在不同的pH和温度下显示出更高的活性,并具有更高的储存稳定性。因此,新型的纳米金/微凝胶颗粒可以作为酶的优良载体。

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