Poly(methacrylic acid) Hydrogel Films and Capsules:  Response to pH and Ionic Strength, and Encapsulation of Macromolecules

Veronika Kozlovskaya(Stevens Institute of Technology), Eugenia Kharlampieva(Stevens Institute of Technology), Marc L. Mansfield(Stevens Institute of Technology), Svetlana A. Sukhishvili(Stevens Institute of Technology)
Chemistry of Materials
December 17, 2005
Cited by 253

Abstract

Hydrogen-bonded multilayers of a neutral polymer (poly(N-vinylpyrrolidone), PVPON) with poly(methacrylic acid) (PMAA) were used as templates to introduce cross-links between PMAA layers using carbodiimide chemistry and ethylenediamine as a cross-linking agent. Upon exposure to high pH, PVPON is completely released from the hydrogel matrix, producing surface-attached PMAA hydrogels. When such hydrogels are deposited at the surface of silica particles, and the particle core is subsequently dissolved, hollow one-component hydrogel capsules are produced. PMAA hydrogel films and hollow capsules underwent reversible, large (factors of 2 or 3) changes in size in response to changes in solution pH and/or ionic strength. The capsules were used for entrapment and storage of macromolecules such as 500 kDa FITC-dextran by “locking” the capsule wall with an electrostatically associating polycation, poly-N-ethyl-4-vinylpyridinium bromide (QPVP). The release of the encapsulated macromolecules was achieved under high salt concentrations (0.6 M NaCl) when QPVP dissociated from the capsule wall. The pH and salt response of these PMAA hydrogel capsules and the polycation-controlled encapsulation of macromolecules hold promise for applications in biomedicine and biotechnology.


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