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Development of new nanostructured materials has shown high impact for improving the performance of chemical and biological sensors. In this work, we show that by controlling the dimensions of the gold flower microelectrode (GFME), it is possible to regulate detection sensitivity of a sensor for rapid analysis of chemical species. A ~13-fold increase in sensitivity was achieved by enlarging the dimension of GFMEs from 70 to 330 μm, whereas the response dynamics are dimension-independent, with the signal attaining saturation ~20 s. Due to the intrinsic nanostructure on the microelectrode surface, our GFME exhibits excellent anti-interference property when applied to detect dopamine (DA) in the presence of 10-fold excess of ascorbic acid (AA). The regulable sensitivity, fast response dynamics, and excellent anti-interference property will make GFME an ideal sensing platform for biomedical applications. [ABSTRACT FROM AUTHOR]

In recent years, poly adenine (polyA) DNA functionalized gold nanoparticles (AuNPs) free of modifications was fabricated with high density of DNA attachment and high hybridization ability similar to those of its thiolated counterpart. This nanoconjugate utilized poly adenine as an anchoring block for binding with the AuNPs surface thereby facilitated the appended recognition block a better upright conformation for hybridization, demonstrating its great potential to be a tunable plasmonic biosensor. It's one of the key points for any of the practical applications to maintaining stable conjugation between DNA oligonucleotides and gold nanoparticles under various experimental treatments. Thus, in this research, we designed a simple but sensitive fluorescence turn-on strategy to systematically investigate and quantified the dissociation of polyA DNA on gold nanoparticles in diverse experimental conditions. DNA desorbed spontaneously as a function of elevated temperature, ion strength, buffer pH, organic solvents and keeping time. What's more, evaluating this conjugate stability as affected by the length of its polyA anchor was another crucial aspect in our study. With the improved understanding from these results, we were able to control some of our experimental conditions to maintain a good stability of this kind of polyA DNA−AuNPs nanoconjugates. [ABSTRACT FROM AUTHOR]