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Updated: May 7, 2026

A Rapid and Quantitative Fluorimetric Method for Protein-Targeting Small Molecule Drug Screening
Published on: October 16, 2015
Molecular engineering of Au25(SG)18 nanoclusters at the single cluster level to brighten their NIR-II fluorescence
Hailiang Zhang1,2, Jing Wang1,2, Wenxiu Han1,2
1Translational Pharmaceutical Laboratory, Jining First People's Hospital, Shandong First Medical University, Jining 272000, China. ppheqq_cool@126.com.
Abstract:
Au25(SG)18 (SG: glutathione) nanoclusters, characterized by their atomically precise structures, exhibit near-infrared II (NIR-II) fluorescence emission and excellent biocompatibility, making them highly promising for imaging applications. However, their comparatively low photoluminescence quantum yield (QY) in aqueous solutions limits their further development. In this study, taking advantage of the molecular-like properties of Au25(SG)18 nanoclusters, we employ a Schiff base reaction to improve their NIR-II emission for the first time. The formation of a Schiff base chemical bond restricts intramolecular motion of surface ligands on the Au25(SG)18 nanoclusters, reduces the nonradiative rate, and increases the radiative transition rate. Consequently, the luminescence quantum yield of PDA-Au25(SG)18 (PDA: 2,6-pyridinedicarboxaldehyde) nanoclusters is enhanced to 3.26%. Moreover, the reaction between amino and aldehyde groups occurs at the single cluster level, ensuring that these PDA-Au25(SG)18 nanoclusters remain discrete with an ultrasmall size of 2.6 nm, facilitating rapid excretion via the renal system and also showing excellent photostability and biocompatibility.

