4.7 Article

Block Copolymer Membranes for Efficient Capture of a Chemotherapy Drug

Journal

ACS MACRO LETTERS
Volume 5, Issue 8, Pages 936-941

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsmacrolett.6b00459

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Funding

  1. Electron Microscopy of Soft Matter Program from the Office of Basic Energy Sciences of the U.S. Department of Energy [DE-AC02-05CH11231]
  2. National Institutes of Health (NIH) [1R01CA194533, 1R41CA183327]

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We introduce the use of block copolymer membranes for an emerging application, drug capture. The polymer is incorporated in a new class of biomedical devices, referred to as ChemoFilter, which is an image-guided temporarily deployable endovascular device designed to increase the efficacy of chemotherapy-based cancer treatment. We show that block copolymer membranes consisting of functional sulfonated polystyrene end blocks and a structural polyethylene middle block (S-SES) are capable of capturing doxonibicin, a chemotherapy drug. We focus on the relationship between morphology of the membrane in the ChemoFilter device and efficacy of doxorubicin capture measured in vitro. Using small-angle X-ray scattering and cryogenic scanning transmission electron microscopy, we discovered that rapid doxorubicin capture is associated with the presence of water-rich channels in the lamellar-forming S-SES membranes in aqueous environment.

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