Plasmon-Enhanced Fluorescence-Based Core-Shell Gold Nanorods as a Near-IR Fluorescent Turn-On Sensor for the Highly Sensitive Detection of Pyrophosphate in Aqueous Solution.

Developing plasmon-enhanced fluorescence (PEF) technology for identifying important biological molecules has a profound impact on biosensing and bioimaging. However, exploration of PEF for biological application is still at a very early stage. Herein, novel PEF-based core-shell nanostructures as a near-infrared fluorescent turn-on sensor for highly sensitive and selective detection of pyrophosphate (PPi) in aqueous solution are proposed. This nanostructure gold nanorod (AuNR)@SiO₂@meso-tetra(4-carboxyphenyl) porphyrin (TCPP) contains a gold nanorod core with an aspect ratio of 2.3, a silica shell, and TCPP molecules covalently immobilized onto the shell surface. The silica shell is employed a rigid spacer for precisely tuning the distance between AuNR and TCPP and an optimum fluorescence enhancement is obtained. Due to the quenching effect of Cu²⁺, the copper porphyrin (TCPP-Cu²⁺) results in a weak fluorescence. In the presence of PPi, the strong affinity between Cu²⁺ and PPi can promote the disassembly of the turn-off state of TCPP-Cu²⁺ complexes, and therefore the fluorescence can be readily restored. By virtue of the amplified fluorescence signal imparted by PEF, this nanosensor obtains a detection limit of 820 × 10^-9m of PPi with a good selectivity over several anions, including phosphate. Additionally, the potential applicability of this sensor in cell imaging is successfully demonstrated. [ABSTRACT FROM AUTHOR]