Synthesis of Acid-Labile PEG and PEG-Doxorubicin-Conjugate Nanoparticles via Brush-First ROMP
Name
Johnson_Synthesis of acid.pdf
Size
1.73 MB
Format
Adobe PDF
Checksum (MD5)
4b8c837e738ebcd204be7eddc2260ad9
Author(s) • •
Gao, Angela X.
Liao, Longyan
Johnson, Jeremiah A.
Date Issued
August 2014
Journal
ACS Macro Letters
Publisher
American Chemical Society (ACS)
Citation
Gao, Angela X., Longyan Liao, and Jeremiah A. Johnson. “Synthesis of Acid-Labile PEG and PEG-Doxorubicin-Conjugate Nanoparticles via Brush-First ROMP.” ACS Macro Letters 3, no. 9 (September 16, 2014): 854–857. © 2014 American Chemical Society.
Version
Final published version
Abstract
A panel of acid-labile bis-norbornene cross-linkers was synthesized and evaluated for the formation of acid-degradable brush-arm star polymers (BASPs) via the brush-first ring-opening metathesis polymerization (ROMP) method. An acetal-based cross-linker was identified that, when employed in conjunction with a poly(ethylene glycol) (PEG) macromonomer, provided highly controlled BASP formation reactions. A combination of this new cross-linker with a novel doxorubicin (DOX)-branch-PEG macromonomer provided BASPs that simultaneously degrade and release cytotoxic DOX in vitro.
MIT Department
Massachusetts Institute of Technology. Department of Chemistry
Terms of Use
Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
Persistent DSpace Link
DOI of Published Version
https://doi.org/10.1021/mz5004097