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- W3164307387 abstract "Communication between biological components is critical for homeostasis maintenance among the convergence of complicated bio-signals. For therapeutic nanoparticles (NPs), the general lack of effective communication mechanisms with the external cellular environment causes loss of homeostasis, resulting in deprived autonomy, severe macrophage-mediated clearance, and limited tumor accumulation. Here, we develop a multistage signal-interactive system on porous silicon particles through integrating the Self-peptide and Tyr-Ile-Gly-Ser-Arg (YIGSR) peptide into a hierarchical chimeric signaling interface with don't eat me and eat me signals. This biochemical transceiver can act as both the signal receiver for amantadine to achieve NP transformation and signal conversion as well as the signal source to present different signals sequentially by reversible self-mimicking. Compared with the non-interactive controls, these signal-interactive NPs loaded with AS1411 and tanespimycin (17-AAG) as anticancer drugs improve tumor targeting 2.8-fold and tumor suppression 6.5-fold and showed only 51% accumulation in the liver with restricted hepatic injury." @default.
- W3164307387 created "2021-06-07" @default.
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- W3164307387 date "2021-05-01" @default.
- W3164307387 modified "2023-10-10" @default.
- W3164307387 title "Multistage signal-interactive nanoparticles improve tumor targeting through efficient nanoparticle-cell communications" @default.
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- W3164307387 doi "https://doi.org/10.1016/j.celrep.2021.109131" @default.
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