Oocyte
quality plays a crucial role in the early development and
implantation of the embryos, and consequently has a profound impact
on the accomplishment of assisted reproductive technology (ART). A
simple and efficient method for detecting high-quality human oocytes
is urgently needed. However, the clinically used morphological method
is time-consuming, subjective, and inaccurate. To this end, we propose
a practical and effective approach for detecting high-quality oocytes
via on-chip measurement of the oocyte membrane permeability. We found
that oocytes can be divided into two subpopulations (high-quality
versus poor-quality oocytes) according to their membrane permeability
differences, and as was further confirmed by subsequent in
vitro fertilization (IVF) and development experiments (the
blastocyst rates of high-quality and poor-quality oocytes were 60%
and 0%, respectively). This approach shows great potentials in improving
the success of ART, including both the fertilization and development
rates, and thus it may have wide applications in the clinic.