Abstract
Local, sustained release and presentation of RNAi therapeutics can be achieved with hydrogel delivery systems. Here we show the development of a supramolecular hydrogel into a local RNAi delivery system. By careful material design, two simple but effective strategies are introduced to obtain controlled release of two classes of RNAi therapeutics, that is, microRNA and antimiR. It was shown that the release of microRNA could be regulated using cholesterol-modification for interaction with the supramolecular hydrogel. Non-modified antimiR release could be controlled via supramolecular introduction of positively charged additive molecules into the supramolecular hydrogel. In this way, either the cholesterol-modification on the drug or the charge introduction into the hydrogel provides handles for controlled RNAi therapy.
| Original language | English |
|---|---|
| Pages (from-to) | 3501-3508 |
| Number of pages | 8 |
| Journal | Chemistry - An Asian Journal |
| Volume | 13 |
| Issue number | 22 |
| DOIs | |
| Publication status | Published - 16 Nov 2018 |
Funding
This work was supported by the Ministry of Education, Culture and Science (Gravity program 024.001.035) and the European Research Council (FP7/2007–2013) ERC Grant Agreement 308045. We acknowledge the support from the Netherlands Cardiovascular Research Initiative: an initiative with support of the Dutch Heart Foundation, CVON2014-27 REMAIN. The authors thank Christina Dalby from miRagen Therapeutics for providing several of the RNAi therapeutics and E.W. Meijer for helpful discussions.
Keywords
- affinity
- controlled release
- drug-delivery systems
- injectable
- RNAi
- supramolecular hydrogels
- Viscosity
- Fluorescence Recovery After Photobleaching
- Cholesterol/chemistry
- Rheology
- Humans
- Hydrogels/chemistry
- Antagomirs/chemistry
- Drug Carriers/chemistry
- RNA Interference
- Polyethylene Glycols/chemistry
- RNA, Small Interfering/chemistry
- HEK293 Cells
- Drug Liberation
- Hydrogen-Ion Concentration
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