Typical
aggregation-induced emission (AIE) luminogens tetraphenylethylene
(TPE) and triphenylamine have been used to construct an AIE-active
conjugated polymer, namely, poly(N,N-diphenyl-4-(4-(1,2,2-triphenylvinyl)styryl)aniline) (PTPA), which
consist of D−π–A architecture by Wittig polymerization.
We fabricated mesoporous silica hollow nanospheres (MSHNs) which were
encapsulated with the AIE-active polymer for applications in cellular
imaging. It exhibits a positive solvatochromism effect by increasing
solvent polarity, supported by theoretical calculation using density
functional theory. The structure of the monomers and polymer was confirmed
by Fourier transform infrared, nuclear magnetic resonance, and high-resolution
mass spectrometry techniques. Considering the advantage of high brightness
in the fluorescence of PTPA, it was encapsulated into MSHNs by a noncovalent
approach, and the surface was functionalized with an anti-EpCAM (antiepithelial
cell adhesion molecule) aptamer through conjugation with γ-glycidoxypropyltrimethoxysilane
for targeting cancer cells specifically. The aptamer-functionalized
Apt-MSHNs exhibited excellent biocompatibility with the liver cancer-Huh-7
cells used for this study and was efficiently internalized by these
cells. Because EpCAM are overexpressed in multiple carcinomas, including
liver cancer, these aptamer-conjugated AIE MSHNs are therefore good
candidates for targeted cellular imaging applications.