Abstract
Multidomain peptide (MDP) nanofibers create scaffolds that can present bioactive cues to promote biological responses. Orthogonal self-assembly of MDPs and growth-factor-loaded liposomes generate supramolecular composite hydrogels. These composites can act as delivery vehicles with time-controlled release. Here we examine the controlled release of placental growth factor-1 (PlGF-1) for its ability to induce angiogenic responses. PlGF-1 was loaded either in MDP matrices or within liposomes bound inside MDP matrices. Scaffolds showed expected rapid infiltration of macrophages. When released through liposomes incorporated in MDP gels (MDP(Lipo)), PlGF-1 modulates HUVEC VEGF receptor activation in vitro and robust vessel formation in vivo. These loaded MDP(Lipo) hydrogels induce a high level of growth-factor-mediated neovascular maturity. MDP(Lipo) hydrogels offer a biocompatible and injectable platform to tailor drug delivery and treat ischemic tissue diseases.
Original language | English (US) |
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Pages (from-to) | 845-854 |
Number of pages | 10 |
Journal | ACS Biomaterials Science and Engineering |
Volume | 1 |
Issue number | 9 |
DOIs | |
State | Published - Sep 14 2015 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Biomaterials
- Biomedical Engineering
Keywords
- PlGF-1
- angiogenesis
- cellular infiltration
- liposomal encapsulation
- multidomain peptide
- self-assembly