Dual-Mode FL-SERS Biosensor for Self-Validating H 2 S Detection in Complex Matrices and Mitochondria-Targeted Cellular Imaging

作者：Yang Shen, Yun Wang, Yilin Long, Yuting Zhang, Xiaoli Wang, Nandi Zhou · 发表于：Analytical Chemistry · 年份：2026 · DOI：10.1021/acs.analchem.6c00460 · 被引用次数：1 · 研究领域：Sulfur Compounds in Biology、Advanced Nanomaterials in Catalysis、Gold and Silver Nanoparticles Synthesis and Applications

Hydrogen sulfide (H 2 S) plays dual-faced roles in physiological regulation and food quality, demanding detection tools with high sensitivity, specificity, and self-validating capability. Herein, a dual-mode biosensor integrating fluorescence (FL) and surface-enhanced Raman scattering (SERS) is developed for ultrasensitive detection and mitochondrial-targeted imaging of H 2 S. The biosensor is constructed based on an azide-functionalized metal–organic framework (UiO-66-N 3 ) coupled with gold nanoparticles (AuNPs), where the electron-withdrawing −N 3 group serves simultaneously as an FL quencher and a SERS reporter. Upon H 2 S exposure, the selective reduction of −N 3 to −NH 2 triggers an FL turn-on response and a concomitant SERS signal attenuation. This dual-response mechanism allows for quantitative H 2 S detection across a wide dynamic range (0.01–500 nM), with detection limits reaching as low as the pM level. Further functionalization with a mucin1 aptamer and a mitochondrial localization sequence empowers tumor-specific mitochondrial targeting and high-fidelity imaging of endogenous H 2 S. The biosensor demonstrates robust applicability in complex beer and wine samples and enables real-time tracking of mitochondrial H 2 S fluctuations in living cells. This work establishes a versatile and self-validating sensing platform that bridges materials design with practical bioanalysis, highlighting its broad potential in food safety monitoring and biomedical diagnostics.