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Malathion is a toxic organophosphorus pesticide. When ingested by humans, it affects the nervous system and endangers health. Herein, a new type of aptamer-based sensor was developed for its determination. The results demonstrate that this sensor has high sensitivity and good selectivity and was successfully used for the determination of malathion in apples. The detection mechanism is as follows. The aptamer is adsorbed on the surface of gold nanoparticles (AuNPs) to prevent the aggregation of AuNPs in a high salt solution. After adding malathion, the aptamer specifically binds to malathion and is removed from the surface of the AuNPs. The quantity of aptamer adsorbed on the surface of AuNPs had a negative relationship with the malathion concentration. The unmodified AuNPs aggregated to different degrees in NaCl solution. In the Fehling reaction, various degrees of aggregated AuNPs catalyze the reduction to different size Cu2O and exhibit different resonance scattering intensities. An excellent linear response between the resonance scattering spectra intensity and malathion concentration was obtained. The limit of detection of the developed method was 5.24 ng/L (15.86 pM). The recovery and repeatability for the apple samples were satisfactory. [ABSTRACT FROM AUTHOR]

• A novel fluorescence switching aptasensor for ultrasensitive detection of Kana was developed. • Aptamer as fluorescence switching was simple to fabricate. • The constructed aptasensor showed high selectivity and accuracy. • The limit of detection, accuracy and recovery rate of the developed fluorescence aptasensor were satisfied. We developed a fluorescent switching based on bovine serum albumin stabilized gold nanoclusters (BSA-AuNCs) and kanamycin (Kana) aptamer to detect Kana. Red fluorescence of BSA-AuNCs was turn off when Kana aptamer was assembled on the surface of BSA-AuNCs. However, after adding Kana, the specific aptamer detached from the surface of the BSA-AuNCs and formed the complex of aptamer-kanamycin, then the red fluorescence of BSA-AuNCs was turn on. The fluorescence intensity of BSA-AuNCs can be mediated by the amount of Kana aptamer. A good linear response for Kana was obtained in the concentration range 0.04 nM to 7.0 nM. The assay was used to detect Kana in milk matrix, and the accuracy and recovery of the method were satisfied. It is worth noting that the aptamer mediated BSA-AuNCs fluorescent switching was simple and easy to fabricate, which can provide a novel assay for the detection of small molecules. [ABSTRACT FROM AUTHOR]