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基于添加剂的生物设计的 CuO 和 GSH-CuO 纳米球的稳定性评估及其作为纳米生物传感器的适用性。

Additive-based stability assessment of biologically designed CuO and GSH-CuO nanospheres and their applicability as Nano-biosensors.

机构信息

Microbiology and Biotechnology Research Lab, Department of Biotechnology, Fatima Jinnah Women University. Pakistan Old Presidency, the Mall, Rawalpindi, 46000, Pakistan.

出版信息

Colloids Surf B Biointerfaces. 2019 Jun 1;178:66-73. doi: 10.1016/j.colsurfb.2019.02.048. Epub 2019 Feb 23.

Abstract

Uncapped and Glutathione capped Cupric oxide nanospheres were synthesized by the interaction of Berberis lycium (Bl) root extract with corresponding salt solution. CuO nanospheres were best optimized by mixing 2% Bl extract solution with 1 mM CuSO·5HO (pH 11, 90 °C) Reduced glutathione (0.25 mM) in solution form was added in respective emulsion after 24 h. Synthesis of nanospheres was ensured by distinct surface plasmonic resonance peaks shown by CuO (370-420 nm). Addition of glutathione resulted in sharp blue shift and lowered absorbance values in UV spectra suggesting the decrease in nanoparticles' size and concentration. Average particle sizes as deduced with XRD were found to be 18.52 and 16.57 nm for CuO and GSH-CuO nanospheres respectively. Additive based stability assessment of synthesized nanospheres revealed CuO and GSH-CuO nanospheres to be highly stable in the presence of Catechin hydrate among various tested chemical compounds while ascorbic acid appeared as a strong destabilizing agent. TMB was oxidized by HO in the presence of synthesized enzymes likewise horseradish peroxidase; though exhibited moderate results. Glutathione stabilized cupric oxide nanospheres exhibited the potential to be modulated further into efficient nanozymes as these showed better affinity towards chromogenic substrate TMB (K value 0.32 mM) and better catalytic efficiency (0.075 mM s) compared to uncapped CuO nanomimetics (1.6 mM, 0.033 mM s). All of the tested additives served as inhibitors to the peroxidase mimicking potential of CuO and GSH-CuO nanozymes.

摘要

无帽和谷胱甘肽帽氧化铜纳米球通过小檗根提取物与相应盐溶液的相互作用合成。通过将 2% Bl 提取物溶液与 1 mM CuSO·5HO(pH 11,90°C)混合,氧化铜纳米球得到最佳优化。还原型谷胱甘肽(0.25 mM)以溶液形式添加到各自的乳液中 24 小时后。氧化铜(370-420nm)显示出明显的表面等离子体共振峰,表明纳米球的合成。谷胱甘肽的加入导致紫外光谱中出现明显的蓝移和吸光度值降低,表明纳米颗粒的尺寸和浓度降低。通过 XRD 推断的平均粒径分别为 18.52nm 和 16.57nm 用于氧化铜和 GSH-CuO 纳米球。基于添加剂的合成纳米球稳定性评估表明,在各种测试的化学化合物中,氧化铜和 GSH-CuO 纳米球在儿茶素水合物存在下高度稳定,而抗坏血酸则表现出很强的去稳定作用。TMB 在HO 的存在下被合成酶氧化,与辣根过氧化物酶一样;尽管结果中等。谷胱甘肽稳定的氧化铜纳米球有可能进一步被修饰成有效的纳米酶,因为与无帽 CuO 纳米模拟物相比,这些纳米球对显色底物 TMB 具有更好的亲和力(K 值为 0.32 mM)和更好的催化效率(0.075 mM·s)(1.6 mM,0.033 mM·s)。所有测试的添加剂都作为氧化铜和 GSH-CuO 纳米酶过氧化物酶模拟潜力的抑制剂。

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