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	<dc:title xml:lang="en-US">Experimental comparison of electrochemical and quantum transport-based biodetection methods for RNA cancer biomarkers</dc:title>
	<dc:creator>Williams, Ajoke</dc:creator>
	<dc:creator>Arachchillage, Keshani Gayathri Gunasinghe Pattiya</dc:creator>
	<dc:creator>Chandra, Subrata</dc:creator>
	<dc:creator>Vivancos, Juan Manuel Artes</dc:creator>
	<dc:subject xml:lang="en-US">KRAS G12V</dc:subject>
	<dc:subject xml:lang="en-US">Single molecule</dc:subject>
	<dc:subject xml:lang="en-US">Bioelectrochemistry</dc:subject>
	<dc:subject xml:lang="en-US">RNA cancer biomarkers</dc:subject>
	<dc:subject xml:lang="en-US">Biomolecular electronics</dc:subject>
	<dc:subject xml:lang="en-US">Electrochemical biosensors</dc:subject>
	<dc:subject xml:lang="en-US">Molecular electronics detection</dc:subject>
	<dc:description xml:lang="en-US">Cancer remains a leading cause of death worldwide and early‑stage detection is essential to improve patient outcomes. Recent advances in nanoscale sensing have opened up new pathways for ultrasensitive, label-free detection of nucleic acid biomarkers. In this work, we compare two sensor platforms for a KRAS G12V RNA biomarker: (i) a classical bioelectrochemical sensor that exploits the redox activity of methylene blue modified DNA probes, and (ii) a recently reported quantum transport-based single-molecule sensor that measures conductance changes of individual DNA: RNA hybrids using scanning ‑ tunneling‑microscopy break‑junctions (STM‑BJ). By comparing both approaches, we evaluate their key performance metrics -limit of detection, specificity, and robustness- in biologically relevant complex media. The electrochemical sensor reaches a femtomolar detection limit, but fails to discriminate a single‑base mismatch under the tested conditions. In contrast, the STM-BJ platform delivers attomolar sensitivity and single-base resolution; however, its operation is hindered in complex media, particularly in protein-rich environments. However, this weakness is also shared with the electrochemical approach. Our comparative analysis highlights the complementary strengths of these platforms, suggesting that integrating both could improve point-of-care cancer screening by combining sensitivity, specificity, and robustness in complex samples.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2026-06-30</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/2748</dc:identifier>
	<dc:identifier>10.5155/eurjchem.17.2.89-98.2748</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 17 No. 2 (2026): June 2026; 89-98</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://www.eurjchem.com/index.php/eurjchem/article/view/2748/3029</dc:relation>
	<dc:rights xml:lang="en-US">Copyright (c) 2026 Ajoke Williams, Keshani Gayathri Gunasinghe Pattiya Arachchillage, Subrata Chandra, Juan Manuel Artes Vivancos</dc:rights>
	<dc:rights xml:lang="en-US">https://creativecommons.org/licenses/by-nc/4.0</dc:rights>
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