Directing biological functions is at the heart of next-generation biomedical initiatives in tissue and immuno-engineering. However, the ambitious goal of engineering complex biological networks requires the ability to precisely perturb specific signaling pathways at distinct times and places. Using lipid nanotechnology and the principles of supramolecular self-assembly, we developed an injectable liposomal nanocomposite hydrogel platform to precisely control the release of multiple protein drugs. By integrating modular lipid nanotechnology into a hydrogel, we introduced multiple mechanisms of release based on liposome surface chemistry. To validate the utility of this system for multi-protein delivery, we demonstrated synchronized, sustained, and localized release of IgG antibody and IL-12 cytokine in vivo , despite the significant size differences between these two proteins. Overall, liposomal hydrogels are a highly modular platform technology with the ability the mediate orthogonal modes of protein release and the potential to precisely coordinate biological cues both in vitro and in vivo .
Keyphrases
- hyaluronic acid
- drug delivery
- tissue engineering
- protein protein
- heart failure
- signaling pathway
- binding protein
- wound healing
- high throughput
- mass spectrometry
- oxidative stress
- epithelial mesenchymal transition
- cell proliferation
- gold nanoparticles
- risk assessment
- quality improvement
- quantum dots
- single cell
- carbon nanotubes
- water soluble
- energy transfer
- solid phase extraction
- tandem mass spectrometry