Abstract
The development of local, intrarenal drug delivery therapies is imperative to induce a therapeutic effect without the requirement of high concentrations of drugs, thereby diminishing systemic side effects. Hydrogels are eminently suitable as drug delivery carriers in soft tissues. Here, we show that a supramolecular hydrogel carrier based on ureido-pyrimidinone (UPy) modified poly(ethylene glycol) can be easily formulated and conveniently be applied to deliver anti-inflammatory and anti-fibrotic growth factor protein BMP7 to the kidney. Short-term, immediate modulation of renal inflammation and extracellular matrix remodelling is shown in a rat model of acute kidney injury. Induction of ischemia/reperfusion injury was followed by renal subcapsular implantation of pristine and BMP7-loaded supramolecular hydrogels. The cortical area under the site of implantation was studied after 3 and 7 days. Subcapsular delivery of only 0.30 mu g BMP7 from these supramolecular hydrogels led to a significant reduction in interstitial inflammatory and myofibroblast cell numbers at the site of implantation. These findings show that local, intrarenal delivery of an anti-inflammatory and anti-fibrotic drug from a supramolecular hydrogel carrier can be effective in the reduction of acute inflammation and incipient fibrosis. (C) 2015 Elsevier Ltd. All rights reserved.
Original language | English |
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Pages (from-to) | 484-493 |
Number of pages | 10 |
Journal | European Polymer Journal |
Volume | 72 |
DOIs | |
Publication status | Published - Nov-2015 |
Keywords
- Drug delivery/release
- Formulation
- Growth factor
- Supramolecular hydrogel
- Kidney
- BONE MORPHOGENETIC PROTEINS
- CHRONIC KIDNEY-DISEASE
- TRANSIENT NETWORKS
- MYOFIBROBLAST
- FIBROSIS
- RATS
- ISCHEMIA/REPERFUSION
- FIBROGENESIS
- HYDROGELS
- INJURY