Self-Assembled Responsive Bilayered Vesicles with Adjustable Oxidative Stress for Enhanced Cancer Imaging and Therapy.

J Am Chem Soc

Laboratory of Molecular Imaging and Nanomedicine (LOMIN), National Institute of Biomedical Imaging and Bioengineering (NIBIB) , National Institutes of Health (NIH), Bethesda , Maryland 20892 , United States.

Published: May 2019

AI Article Synopsis

  • The study focuses on creating magnetic-plasmonic bilayer vesicles using iron oxide-gold Janus nanoparticles (FeO-Au JNPs) to improve chemotherapy by enhancing reactive oxygen species (ROS) generation.
  • The amphiphilic nanoparticles are coated with different compounds, allowing them to self-assemble into vesicles that exhibit superior optical properties and can disassemble in acidic tumor environments, facilitating increased ROS production.
  • Combining these vesicles with the chemotherapy drug doxorubicin (DOX) enhances treatment effectiveness beyond what either the vesicles or DOX can achieve alone, with confirmed efficient tumor targeting and rapid body clearance.

Article Abstract

In the present study, we report the development of magnetic-plasmonic bilayer vesicles assembled from iron oxide-gold Janus nanoparticles (FeO-Au JNPs) for reactive oxygen species (ROS) enhanced chemotherapy. The amphiphilic FeO-Au JNPs were grafted with poly(ethylene glycol) (PEG) on the Au surface and ROS-generating poly(lipid hydroperoxide) (PLHP) on the FeO surface, respectively, which were then assembled into vesicles containing two closely attached FeO-Au NPs layers in opposite directions. The self-assembly mechanism of the bilayered vesicles was elucidated by performing a series of numerical simulations. The enhanced optical properties of the bilayered vesicles were verified by the calculated results and experimental data. The vesicles exhibited enhanced T relaxivity and photoacoustic properties over single JNPs due to the interparticle magnetic dipole interaction and plasmonic coupling. In particular, the vesicles are pH responsive and disassemble into single JNPs in the acidic tumor environment, activating an intracellular biochemical reaction between the grafted PLHP and released ferrous ions (Fe) from FeO NPs, resulting in highly efficient local ROS generation and increased intracellular oxidative stress. In combination with the release of doxorubicin (DOX), the vesicles combine ROS-mediated cytotoxicity and DOX-induced chemotherapy, leading to greatly improved therapeutic efficacy than monotherapies. High tumor accumulation efficiency and fast vesicle clearance from the body were also confirmed by positron emission tomography (PET) imaging of radioisotope Cu-labeled vesicles.

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Source
http://dx.doi.org/10.1021/jacs.8b13902DOI Listing

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