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   <subfield code="a">A Label-Free Nanogold DNAzyme-Cleaved Surface-Enhanced Resonance Raman Scattering Method for Trace UO2 2+ Using Rhodamine 6G as Probe</subfield>
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   <subfield code="a">In pH 5.5 2-(N-morpholino)-ethanosulfonic acid buffer solution containing 0.25M NaCl at 80°C, the single-stranded substrate DNA hybridizes with the enzyme DNA to form double-stranded DNA (dsDNA). The substrate chain of dsDNA could be cracked catalytically by UO2 2+ to produce a short single-stranded DNA (ssDNA) that adsorbed on the nanogold (NG) surface to form a stable nanogold-ssDNA conjugate and then further combine with rhodamine 6G (RhG) to form a NG-ssDNA-RhG conjugate that can be monitored by the surface-enhanced resonance Raman scattering (SERRS) spectral technique at 1,360cm−1. Under the selected conditions, the increased SERRS intensity ΔI 1360 was linear to UO2 2+ concentration in the range of 5-125nmol/L, with a detection limit of 1.6nmol/L. Using a 0.5-μmol/L Hg2+ as enhancer, a 2.5-100-nmol/L UO2 2+ can be determined.</subfield>
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