Ray Chaiti, Dutta Soumen, Sarkar Sougata, Sahoo Ramkrishna, Roy Anindita, Pal Tarasankar
Department of Chemistry, Indian Institute of Technology, Kharagpur-721302, India.
J Mater Chem B. 2014 Sep 28;2(36):6097-6105. doi: 10.1039/c4tb00968a. Epub 2014 Aug 7.
Mesoporous nickel oxide nanoflowers (NiO NFs) can be easily synthesized by a two-step synthetic procedure based on modified hydrothermal (MHT) treatment of nickel acetate and ethanol amine in water followed by thermal decomposition at 350 °C for 4 h. After thermal treatment, the porosity is increased by 18% with retention of parental nickel hydroxide size. In this study, for the first time, a new catalytic application of NiO NFs has been revealed in terms of peroxidase-like activity where colorless 3,3',5,5' tetramethylbenzidine (TMB) is oxidized to blue color product in the presence of HO at room temperature. Comparative study confirms that mesoporous NiO NFs exhibit superior catalytic activity to the parent analogues, i.e. Ni(OH) or bulk NiO. This intrinsic peroxidase-like activity from an easily synthesized inorganic nanomaterial provides an alternative to horseradish peroxidase (HRP) enzyme. The lower Michaelis constant (K) value indicates that the catalyst NiO NFs bind efficiently to the test substrate, i.e. TMB. Interestingly, the NiO NFs-catalyzed TMB oxidation, i.e. blue color formation, has been found to be selectively and successively inhibited by a variable amount of cysteine among a set of 21 congeners. Thus our adopted simple, low-cost and novel colorimetric assay stands to be a highly efficient approach for selective detection of cysteine with a limit of detection (LOD) value of ∼1.1 μM using a simple UV-vis spectrophotometer. The proposed method also exhibits outstanding selectivity and accuracy for N-acetyl cysteine (an analogue of cysteine) estimation in real pharmaceutical samples.
介孔氧化镍纳米花(NiO NFs)可以通过两步合成法轻松合成,该方法基于在水中对醋酸镍和乙醇胺进行改性水热(MHT)处理,然后在350℃下热分解4小时。热处理后,孔隙率增加了18%,同时保留了母体氢氧化镍的尺寸。在本研究中,首次揭示了NiO NFs在类过氧化物酶活性方面的一种新的催化应用,即在室温下,在HO存在的情况下,无色的3,3',5,5'-四甲基联苯胺(TMB)被氧化为蓝色产物。对比研究证实,介孔NiO NFs表现出比母体类似物(即Ni(OH)或块状NiO)更高的催化活性。这种来自易于合成的无机纳米材料的固有类过氧化物酶活性为辣根过氧化物酶(HRP)提供了一种替代方案。较低的米氏常数(K)值表明催化剂NiO NFs能有效地与测试底物(即TMB)结合。有趣的是,发现在一组21种同系物中,不同量的半胱氨酸会选择性地依次抑制NiO NFs催化的TMB氧化,即蓝色的形成。因此,我们采用的简单、低成本且新颖的比色测定法有望成为一种高效的方法,用于使用简单的紫外可见分光光度计选择性检测半胱氨酸,检测限(LOD)值约为1.1μM。所提出的方法在实际药物样品中对N-乙酰半胱氨酸(半胱氨酸类似物)的估计也表现出出色的选择性和准确性。