4.8 Article

Controlled and Triggered Small Molecule Release from a Confined Polymer Film

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 5, Issue 19, Pages 9803-9808

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/am4029894

Keywords

poly (N-isopropylacrylamide)-co-acrylic acid microgels; responsive polymers; controlled release; microgel-based etalon; pH-triggered drug release

Funding

  1. University of Alberta (Department of Chemistry)
  2. Natural Science and Engineering Research Council (NSERC)
  3. Canada Foundation for Innovation (CFI)
  4. Alberta Advanced Education AMP
  5. Technology Small Equipment Grants Program (AET/SEGP)
  6. Grand Challenges Canada
  7. University of Alberta (Faculty of Science)

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A device composed of a poly (N-isopropylacrylamide)-co-acrylic acid (pNIPAm-co-AAc) microgel layer sandwiched between two thin Au layers (all on a glass support) was used as a novel platform for controlled and triggered small molecule delivery. Tris (4-(dimethylamino)phenyl)methylium chloride (Crystal Violet, CV), which is positively charged, was loaded into the microgel layer of the device and released in a pH dependent fashion, at a rate that could be controlled by the thickness of the Au layer coating the microgels. Specifically, at pH 6.5 (above the plc for AAc) the microgels were negatively charged, promoting the strong interaction between the CV and the microgels, hindering its release from the layer. At pH 3.0 the microgel's AAc groups are protonated making the microgel mostly neutral, allowing CV to be released from the microgel layer at a rate that depends on the thickness of the Au covering the microgels. Specifically, devices with thin Au overlayers on the microgel layer allow CV to be released from the device faster than devices with thick Au overlayers. The ability to tune the release rate with pH and Au layer thickness is advantageous for developing implantable devices that are capable of releasing small molecule drugs in a triggered and controlled fashion.

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