4.7 Article

Amino Acid Based Hydrogels with Dual Responsiveness for Oral Drug Delivery

Journal

MACROMOLECULAR BIOSCIENCE
Volume 16, Issue 9, Pages 1258-1264

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/mabi.201600078

Keywords

hydrogel; oral delivery; pH-responsive; redox-responsive

Funding

  1. Marie Curie Actions under EU FP7 Initial Training Network SNAL [608184]

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This study reports a series of novel amino acid based dual-responsive hydrogels. Prepared by a facile one-pot 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) coupling reaction, the solid content, structure, and mechanical behavior of hydrogels could be easily adjusted by changing the concentrations of the polymers and the crosslinkers. With pH-responsive anionic pseudo-peptides as backbones and disulfi de-containing L-cystine dimethyl ester as crosslinkers, these hydrogels are able to collapse and form relatively compact structure at an acidic pH, while swelled and partly dissociated at a neutral pH. Further addition of dithiothreitol (DTT) facilitated complete degradation of hydrogels. The high loading efficiency, rapid but complete triggered-release, and good biocompatibility make these hydrogels promising candidates for oral delivery.

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