首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Electrochemically decorated network-like cobalt oxide nanosheets on nickel oxide nanoworms substrate as a sorbent for the thin film microextraction of diclofenac
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Electrochemically decorated network-like cobalt oxide nanosheets on nickel oxide nanoworms substrate as a sorbent for the thin film microextraction of diclofenac

机译:在氧化镍纳米线衬底上电化学装饰的网络状钴氧化物纳米片作为双氯芬酸的薄膜微萃取的吸附剂

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The network-like cobalt oxide was electrochemically prepared on the nickel oxide nanoworms (NiONWs) which were created on the surface of a nickel film (NF) substrate. Firstly, a very thin layer of NiO nanoworms was successfully grown on the anodized Ni foil. Thereafter, the 3D Co3O4 nanosheets were directly electrodeposited on a-NF/NiONWs by using cyclic voltammetry. The prepared NF/NiONWs/Co3O4 was used as a sorbent for the thin film microextraction (TFME) of diclofenac as the model compound in biological fluids for the first time. The extracted diclofenac was then analyzed by high performance liquid chromatography-ultraviolet detection (HPLC-UV). A Plackett-Burman design was performed for screening the experimental factors to specify the significant variables affecting the performance of the method. The effective factors were then optimized using Box-Behnken design (BBD). Under the optimum condition, the limit of detection (LOD) in water matrix was 0.15 mu g L-1. Limit of quantification (LOQ) was also 0.58 mu g L-1. Relative standard deviation for the analyte extraction at the spiked concentration of 5 mu g L-1 was 4.7% (as intra-day RSD). Film to film reproducibility at the spiked concentration of 100 mu g L-1 was also 6.8%. The linearity of the method in water, urine and plasma matrix was in the range of 1-200, 1-200 and 2-100 mu g L-1, respectively. The capability of the film was investigated by extraction and determination of diclofenac in different biological fluids including urine and plasma samples.
机译:在镍氧化物纳米线(NIONW)上在镍膜(NF)底物的表面上产生的氧化镍纳米线(NiONW)上电化学制备了网状钴氧化物。首先,在阳极氧化Ni箔上成功地生长了一层非常薄的NiO纳米族。此后,通过使用循环伏安法直接在A-NF / nionW上直接电沉积3D CO3O4纳米片。制备的NF / NIONWS / CO3O4用作二氯芬酸的薄膜微萃取(TFME)作为生物流体中的模型化合物的吸附剂。然后通过高效液相色谱 - 紫外检测(HPLC-UV)分析提取的双氯芬酸。进行Plackett-Burman设计,用于筛选实验因素,以指定影响方法性能的重要变量。然后使用Box-Behnken Design(BBD)优化有效因素。在最佳条件下,水基质中的检测极限为0.15μgl-1。量化限制(LOQ)也是0.58μgl-1。用于掺入浓度为5μg-1的分析物提取的相对标准偏差为4.7%(作为日内RSD)。薄膜以100μg1-1的尖刺浓度膜再现性也为6.8%。水,尿液和血浆基质中方法的线性分别为1-200,1-200和2-100μg1-1。通过提取和测定不同生物流体中的双氯芬酸,包括尿液和血浆样品的不同生物液体来研究膜的能力。

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