Extracellular Matrix Encasement Structures and Methods
US-2015359939-A1 · Dec 17, 2015 · US
US9283302B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9283302-B2 |
| Application number | US-201313896424-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 17, 2013 |
| Priority date | Dec 16, 2011 |
| Publication date | Mar 15, 2016 |
| Grant date | Mar 15, 2016 |
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Official abstract text for this publication.
A remodelable encasement structure comprising a pouch formed from at least one sheet of bioremodelable material, the pouch including an internal region and at least one lead conduit, the internal region being configured to receive a device therein, the lead conduit being configures to receive at least one device lead therein, the bioremodelable material comprising an extracellular matrix (ECM) composition that includes an ECM component derived from a mammalian source.
Opening claim text (preview).
What is claimed is: 1. An implantable medical device, comprising: a coated pacemaker comprising an outer surface having at least one coating comprising an extracellular matrix (ECM) composition disposed thereon, said ECM composition coating forming a sealed ECM encasement structure, said ECM composition comprising acellular first ECM from a first mammalian tissue source, said first mammalian tissue source being selected from the group consisting of small intestine submucosa (SIS), urinary bladder submucosa (UBS) and stomach submucosa (SS), said ECM composition further comprising a first bioactive component comprising a statin and a second bioactive component comprising an anti-viral agent, said statin being dispersed within said first ECM, said coated pacemaker, when implanted in host tissue of a subject's body, being configured to modulate said subject's heart rate and induce modulated healing, said modulated healing comprising control of inflammation of said host tissue and induced tissue proliferation and bioremodeling of said host tissue. 2. The coated pacemaker of claim 1 , wherein said ECM composition further comprises acellular second ECM from a second mammalian tissue source, said second mammalian tissue source being selected from the group consisting of urinary basement membrane (UBM) and liver basement membrane (LBM). 3. The coated pacemaker of claim 1 , wherein said ECM composition further comprises a third bioactive component, said third bioactive component comprising a growth factor selected from the group consisting of a platelet derived growth factor (PDGF), epidermal growth factor (EGF), transforming growth factor alpha (TGF-alpha), transforming growth factor beta (TGF-beta), fibroblast growth factor-2 (FGF-2), basic fibroblast growth factor (bFGF), vascular epithelial growth factor (VEGF), hepatocyte growth factor (HGF), insulin-like growth factor (IGF), nerve growth factor (NGF), tumor necrosis factor alpha (TNA-alpha), and placental growth factor (PLGF). 4. The medical device of claim 1 , wherein said statin is selected from the group consisting of atorvastatin, cerivastatin, fluvastatin, lovastatin, mevastatin, pitavastatin, pravastatin, rosuvastatin and simvastatin.
Mixtures of macromolecular compounds · CPC title
multilayered, e.g. laminated structures · CPC title
characterised by specific cells or progenitors thereof, e.g. fibroblasts, connective tissue cells, kidney cells · CPC title
Macromolecular materials · CPC title
Vascular tissue, e.g. heart valves · CPC title
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