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

Abstract

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)@SiO 2 @ 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 Cu 2+ , the copper porphyrin (TCPP‐Cu 2+ ) results in a weak fluorescence. In the presence of PPi, the strong affinity between Cu 2+ and PPi can promote the disassembly of the turn‐off state of TCPP‐Cu 2+ 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 −9 m of PPi with a good selectivity over several anions, including phosphate. Additionally, the potential applicability of this sensor in cell imaging is successfully demonstrated.