Inflammation‐Controlled Anti‐Inflammatory Hydrogels
Source abstract
Abstract
Abstract While autoregulative adaptation is a common feature of living tissues, only a few feedback‐controlled adaptive biomaterials are available so far. This paper herein reports a new polymer hydrogel platform designed to release anti‐inflammatory molecules in response to the inflammatory activation of human blood. In this system, anti‐inflammatory peptide drugs, targeting either the complement cascade, a complement receptor, or cyclophilin A, are conjugated to the hydrogel by a peptide sequence that is cleaved by elastase released from activated granulocytes. As a proof of concept, the adaptive drug delivery from the gel triggered by activated granulocytes and the effect of the released drug on the respective inflammatory pathways are demonstrated. Adjusting the gel functionalization degree is shown to allow for tuning the drug release profiles to effective doses within a micromolar range. Feedback‐controlled delivery of covalently conjugated drugs from a hydrogel matrix is concluded to provide valuable safety features suitable to equip medical devices with highly active anti‐inflammatory agents without suppressing the general immunosurveillance.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Signaling Pathways in Disease · Polymer Surface Interaction Studies · Biochemical and Structural Characterization
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Leibniz Institute of Polymer Research Dresden Institute of Biofunctional Polymer Materials Hohe Strasse 6 01069 Dresden Germany
Max Planck Institute for Multidisciplinary Sciences 37077 Göttingen Germany
Technische Universität Dresden Cluster of Excellence Physics of Life Center for Regenerative Therapies Dresden and Faculty of Chemistry and Food Chemistry Fetscherstraße 105 01307 Dresden Germany
Funding
Bundesministerium für Bildung und Forschung
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