Electrostatic loading and photoredox-based release of molecular cargo from oligoviologen-crosslinked microparticles

Mark S. Palmquist, Max C. Gruschka, Jovelt M. Dorsainvil, Abigail O. Delawder, Tiana M. Saak, Mary K. Danielson, Jonathan C. Barnes

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Although on-demand cargo release has been demonstrated in a wide range of microparticle platforms, many existing methods lack specific loading interactions and/or involve permanent damage to the microparticle to release the cargo. Here, we report a novel method for electrostatically loading negatively charged molecular cargo in oligoviologen-crosslinked microparticles, wherein the cargo can be released upon activation by visible light. A water-in-oil (W/O) emulsion polymerization method was used to fabricate narrowly dispersed microparticles crosslinked by a dicationic viologen-based dimer and a poly(ethylene glycol) diacrylate. A zinc-tetraphenyl porphyrin photocatalyst was also polymerized into the microparticle and used to photochemically reduce the viologen subunits to their monoradical cations through a visible-light-mediated photoredox mechanism with triethanolamine (TEOA) as a sacrificial reductant. The microparticles were characterized by microscopy methods revealing uniform, spherical microparticles 481 ± 20.9 nm in diameter. Negatively charged molecular cargo (methyl orange, MO) was electrostatically loaded into the microparticles through counteranion metathesis. Upon irradiation with blue (450 nm) light, the photo-reduced viologen crosslinker subunits lose positive charges, resulting in release of the anionic MO cargo. Controlled release of the dye, as tracked by absorption spectroscopy, was observed over time, yielding release of up to 40% of the cargo in 48 h and 60% in 120 h in a single dynamic dialysis experiment. However, full release of cargo was achieved upon transferring the microparticles to a fresh TEOA solution after the initial 120 h period.

Original languageEnglish
Pages (from-to)2115-2122
Number of pages8
JournalPolymer Chemistry
Volume13
Issue number15
DOIs
StatePublished - Mar 16 2022

Funding

We thank the David and Lucile Packard Foundation for J.C.B.'s Packard Fellowship for Science and Engineering which supported this research. M. S. P. acknowledges support from the Department of Defense (DoD) through the National Defense Science & Engineering Graduate (NDSEG) Fellowship program. A. O. D. acknowledges support from the National Science Foundation Graduate Research Fellowship Program (NSF GRFP; DGE-1745038) and PEO International Scholar Award. T. M. S. acknowledges support from the American Chemical Society Division of Organic Chemistry's Summer Undergraduate Research Fellowship program. The mass spectrometry data was obtained using the NIH/NIGMS Biomedical Mass Spectrometry Resource at WUSTL, which was supported by a grant from the National Institutes of Health/National Institute of General Medical Sciences (#8P41GM103422).

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