There
is a great deal of interest in the development of nanoparticles
for biomedicine. The question of how many nanoparticles are taken
up by cells is important for biomedical applications. Here, we describe
a fluorescence method for the quantitative measurement of the cellular
uptake of polymer dots (Pdots) and a further estimation of intracellular
Pdots photosensitizer for fluorescence imaging and photodynamic therapy.
The approach relies on the high brightness, excellent stability, minimal
aggregation quenching, and metalloporphyrin doping properties of the
Pdots. We correlated the single-cell fluorescence brightness obtained
from fluorescence spectrometry, confocal microscopy, and flow cytometry
with the number of endocytosed Pdots, which was validated by inductively
coupled plasma mass spectrometry. Our results indicated that, on average,
∼1.3 million Pdots were taken up by single cells that were
incubated for 4 h with arginine 8-Pdots (40 μg/mL, ∼20
nm diameter). The absolute number of endocytosed Pdots of individual
cells could be estimated from confocal microscopy by comparing the
single-cell brightness with the average intensity. Furthermore, we
investigated the cell viability as a result of an intracellular Pdots
photosensitizer, from which the half maximal inhibitory concentration
was determined to be ∼7.2 × 105 Pdots per cell
under the light dose of 60 J/cm2. This study provides an
effective method for quantifying endocytosed Pdots, which can be extended
to investigate the cellular uptake of various conjugated polymer carriers
in biomedicine.