Detection of circulating tumor cells (CTCs) is important
for early
cancer diagnosis, prediction of postoperative recurrence, and individualized
treatment. However, it is still challenging to achieve efficient capture
and gentle release of CTCs from the complex peripheral blood due to
their rarity and fragility. Herein, inspired by the three-dimensional
(3D) network structure and high glutathione (GSH) level of the tumor
microenvironment (TME), a 3D stereo (3D-G@FTP) fibrous network is
developed by combining the liquid-assisted electrospinning method,
gas foaming technique, and metal–polyphenol coordination interactions
to achieve efficient trapping and gentle release of CTCs. Compared
with the traditional 2D@FTP fibrous scaffold, the 3D-G@FTP fibrous
network could achieve higher capture efficiency (90.4% vs 78.5%) toward
cancer cells in a shorter time (30 min vs 90 min). This platform showed
superior capture performance toward heterogeneous cancer cells (HepG2,
HCT116, HeLa, and A549) in an epithelial cell adhesion molecule (EpCAM)-independent
manner. In addition, the captured cells with high cell viability (>90.0%)
could be gently released under biologically friendly GSH stimulus.
More importantly, the 3D-G@FTP fibrous network could sensitively detect
4–19 CTCs from six kinds of cancer patients’ blood samples.
We expect this TME-inspired 3D stereo fibrous network integrating
efficient trapping, broad-spectrum recognition, and gentle release
will promote the development of biomimetic devices for rare cell analysis.