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Magnetically Actuated Active Deep Tumor Penetration of Deformable Large Nanocarriers for Enhanced Cancer Therapy
The intrinsic pathological microenvironment of tumor tissue enforces barriers to the passive diffusion of nanomedicine, which results in inefficient tumor penetration of drugs and unsatisfactory therapeutic efficacy. Various strategies have been developed to improve the tumor penetration of nanomedi...
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Published in: | Advanced functional materials 2021-08, Vol.31 (35), p.n/a |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The intrinsic pathological microenvironment of tumor tissue enforces barriers to the passive diffusion of nanomedicine, which results in inefficient tumor penetration of drugs and unsatisfactory therapeutic efficacy. Various strategies have been developed to improve the tumor penetration of nanomedicine, but they mostly overcome the barriers separately at different steps in a passive diffusion process. Here, the development of a large polymeric nanocarrier, DAT‐PPED&F (≈180 nm), is reported, which comprises a flowable polyphosphoester core, ferrimagnetic nanocubes, and a tumor extracellular pH‐sensitive transactivator of transcription (TAT). Compared with a polylactic acid‐based nanocarrier with a rigid core, this deformable DAT‐PPED&F with a similar diameter exhibits efficient penetration into the deep tumor tissue under magnetic actuation and an enhanced reactivation rate of the pHe‐sensitive TAT. Therefore, DAT‐PPED&F is able to efficiently deliver doxorubicin into most tumor cells in vivo, and the superior anticancer effect indicates the potential of DAT‐PPED&F as a universal, responsive, and active nanocarrier to deliver various hydrophobic drugs into the deep tumor tissue.
A doxorubicin/ferrimagnetic nanocube‐loaded nanoparticle DAT‐PPED&F with deformation capacity is developed for active tumor penetration. DAT‐PPED&F can be efficiently infiltrated into deep tumor tissue under magnetic actuation due to its unique deformation capacity. Moreover, the 2,3‐dimethylmaleic anhydride‐masked transactivator of the transcription peptide of DAT‐PPED&F is efficiently reactivated in the deeper tumor tissue to improve tumor cellular uptake for cancer therapy. |
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ISSN: | 1616-301X 1616-3028 |
DOI: | 10.1002/adfm.202103655 |