A novel colorimetric sensing platform based on the peroxidase activity of hemin regulated by oligonucleotide and pesticide was reported for the ultrasensitive and selective detection of isocarbophos. Oligonucleotides can accumulate on the surface of hemin in acid condition and temporarily inhibit its catalytic activity, which results in the loss of one electron of TMB molecule and produce the blue products. With the addition of isocarbophos, the pesticide molecules can interact with oligonucleotides to form some complexes, which relieve the inhibition of ssDNA to hemin and further enhance its catalytic activity. Thus, the TMB molecules are further oxidized to lose another electron and produce the yellow product in a few minutes, which has the characteristic absorption peak at 450 nm. The color change of the sensing system is related to the amount of isocarbophos, so this method can quickly discriminate whether the target pesticide exceeds the maximal residue limit just by naked eyes. To improve the performance of sensing platform, some important parameters like buffer condition and ssDNA have been investigated, and the peroxidase activity of hemin was further studied to verify the catalytic mechanism. The proposed sensing platform has a detection limit as low as 0.6 μg/L and displays good selectivity against other competitive pesticides. Moreover, the developed sensing platform also exhibits favorable accuracy and stability, indicating that it has potential applications in the detection of pesticide residues in agricultural products.
In this communication, we demonstrate our recent finding that iron-substituted SBA-15 (Fe-SBA-15) microparticles possess intrinsic peroxidase-like activity and can catalyze the oxidation of peroxidase substrate 3,3',5,5'-tetramethylbenzidine (TMB) by H(2)O(2) to develop a blue color in aqueous solution, leading to a simple approach towards colorimetric detection of H(2)O(2) with a linear detection range from 0.4 μM to 15 μM (r = 0.997) and a detection limit of 0.2 μM. 相似文献
In the present work, WO3 nanosheets(WO3 NSs) were prepared by a facile method at room temperature. The obtained WO3 NSs showed peroxidase-like activity, which could catalyze 3,3',5,5'-tetramethylbenzidine(TMB) to form a blue oxidation product(ox TMB) in the presence of H2O2. Based on this, convenient and sensitive colorimetric methods for the detection of H2O2 and glucose were established. The linear ranges for detecting H2O2 and glucose were 1-200 μmol/L and 1-100 μmol/L, respectively. The limits of the detection of H2O2 and glucose were as low as 0.79 and 0.96 μmol/L, respectively. This method was also successfully applied to the detection of glucose in urine samples. The detection result was consistent with that of the value detected by the clinical method, indicating the potential in clinical diagnosis and biomedical detection. 相似文献
Biomass-carbon dots(named as B-CDs) have been successfully prepared via facile one-step hydrothermal reflux treatment at a low temperature from passion fruit peel. The as-prepared B-CDs had a uniform sphere morphology and size of 1-3 nm, which possessed rich nitrogen/oxygen-containing functional groups. B-CDs could imitate peroxidase and accelerate the reaction process of H2O2 oxidizing the substrate 3,3',5,5'-tetramethylbenzidine(TMB), which caused an obvious color change in the solution due to the oxidization of achromic TMB into blue oxidation product(ox-TMB) with an absorption peak at 652 nm. Furthermore, the product could be further reduced to native colorless TMB by the reducing agent glutathione or L-Cysteine. Thus, depending on the peroxidase-like properties of B-CDs, we developed a colorimetric approach to detecting both glutathione and L-Cysteine, which showed superior selective and sensitive detection towards glutathione and L-Cysteine in a linear range of 0-20 µmol/L. The limits of detection were 0.62 and 0.58 µmol/L, respectively. 相似文献