Adenosine,an endogenous nucleoside,has received intense attention due to its multiple important functions related to the physiology of the heart and brain.At the same time,it was consensually identified as a major local regulator of tissue function and honored as a ‘‘retaliatory metabolite’’ for its ability to equalize energy intake to metabolic demand.Recently,adenosine was found to provide a possible link with cancer and it has been reported as a biomarker for monitoring the progress of lung cancer.Hence,accurate detection and quantification of adenosine is of great significance.In this paper,a novel turn-on fluorescence aptasensor was designed for adenosine detection based on fluorescence resonance energy transfer(FRET)from single-stranded DNA labeled carbon dots(ss DNA-CDs)to aptamer modified gold nanoparticles(aptamer-Au NPs).In the absence of adenosine,the fluorescence of ss DNA-CDs was quenched by aptamer-Au NPs via the formation of an aptamer-ss DNA duplex.The introduced adenosine competed to displace ss DNA-CDs by specifically binding to the aptamer,resulting in the recovery of the quenched fluorescence of ss DNA-CDs.Under optimized conditions,the increase in fluorescence intensity was proportional to the concentration of adenosine with a linear range of 10-500 n M and allowed a limit of detection as low as 4.2 n M.In addition,this method was successfully applied to adenosine determination in human serum samples with satisfactory results. |