Energy augmentation structures, energy emitters or energy collectors containing the same, and their use in solar cells and other energy conversion devices
US-2024115878-A1 · Apr 11, 2024 · US
US9327000B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9327000-B2 |
| Application number | US-201514711492-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 13, 2015 |
| Priority date | Jan 18, 2006 |
| Publication date | May 3, 2016 |
| Grant date | May 3, 2016 |
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Methods for treating a cardiovascular disorder comprising administration of one or more extracellular matrix (ECM) based compositions directly to damaged or diseased cardiovascular tissue associated with the cardiovascular disorder, and provision of ventricular assistance.
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What is claimed is: 1. A method of treating a cardiovascular disorder in a subject, comprising: providing an extracellular matrix (ECM) composition comprising acellular ECM, said acellular ECM comprising endogenous proteoglycans, transforming growth factor-β (TGF-β) and vascular endothelial growth factor (VEGF), said ECM composition further comprising an added growth factor selected from the group consisting of fibroblast growth factor-2 (FGF-2), basic fibroblast growth factor (bFGF), transforming growth factor-alpha (TGF-α), transforming growth factor-beta (TGF-β), and vascular epithelial growth factor (VEGF), wherein, when said ECM composition is administered to damaged cardiovascular tissue, said growth factor augmented ECM composition induces myofibroblast and stem cell migration, and differentiation of said stem cells into cardiomyocytes; providing a mechanical circulatory support (MSC) device that is configured to support ventricular function of a mammalian heart when connected thereto; connecting said MSC device to said subject's circulatory system; administering said ECM composition proximate damaged cardiovascular tissue of said subject's heart, wherein said ECM composition induces neovascularization and bioremodeling of said subject's damaged cardiovascular tissue; and providing support of ventricular function of said subject's heart with said MSC device. 2. The method of claim 1 , wherein said ECM comprises ECM from mammalian tissue selected from the group consisting of small intestine submucosa, urinary bladder submucosa, stomach submucosa, placental tissue, mesothelial tissue, ornomentum tissue and kidney tissue. 3. The method of claim 1 , wherein said ECM composition is administered directly to said subject's damaged cardiovascular tissue.
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