It
is generally known that, for nanoparticles in cancer therapy, sufficient
tumor penetration needs a minor particle size, while long in vivo
circulation time needs a larger particle size. It is hard to balance
them because they are standing on either side of a seesaw. To address
these two different requirements, a dual-responsive size-shrinking
nanocluster can self-adaptively respond to a complicated tumor microenvironment
and transform its particulate property to overcome sequential in vivo
barriers and reach a preferable antitumor activity. The nanocluster
(RPSPT@SNCs) could preferentially accumulate into tumor tissue and
dissociate under extracellular matrix metalloproteinase-2 (MMP-2)
to release small-sized micelle formulations (RPSPTs). RPSPT possesses
favorable tumor penetration and tumor targeting capability to deliver
the antitumor agent paclitaxel (PTX) into deep regions of solid tumor.
The intracellular redox microenvironment can also accelerate drug
accumulation. The prepared RPSPT@SNCs possesses enhanced cell cytotoxicity
and tumor penetration capability on MCF-7 cells and a favorable antitumor
activity on the xenograft tumor mouse model.