Semiconducting
polymer dots (P-dots) recently have emerged as a
new type of ultrabright fluorescent probe with promising applications
in biological imaging and detection. With the increasing desire for
near-infrared (NIR) fluorescing probes for in vivo biological measurements,
the currently available NIR-emitting P-dots are very limited and the
leaching of the encapsulated dyes/polymers has usually been a concern.
To address this challenge, we first embedded the NIR dyes into the
matrix of poly[(9,9-dioctylfluorene)-co-2,1,3-benzothiadiazole-co-4,7-di(thiophen-2-yl)-2,1,3-benzothiadiazole] (PF-BT-DBT)
polymer and then enclosed the doped P-dots with polydiacetylenes (PDAs)
to avoid potential leakage of the entrapped NIR dyes from the P-dot
matrix. These PDA-enclosed NIR-emitting P-dots not only emitted much
stronger NIR fluorescence than conventional organic molecules but
also exhibited enhanced photostability over CdTe quantum dots, free
NIR dyes, and gold nanoclusters. We next conjugated biomolecules onto
the surface of the resulting P-dots and demonstrated their capability
for specific cellular labeling without any noticeable nonspecific
binding. To employ this new class of material as a facile sensing
platform, an easy-to-prepare test paper, obtained by soaking the paper
into the PDA-enclosed NIR-emitting P-dot solution, was used to sense
external stimuli such as ions, temperature, or pH, depending on the
surface functionalization of PDAs. We believe these PDA-coated NIR-fluorescing
P-dots will be very useful in a variety of bioimaging and analytical
applications.