Technology ID
TAB-5111

iPSC Differentiation Protocol for Fibroblast and Endothelial Cell Generation

E-Numbers
E-007-2023-0
Lead Inventor
Park, Tea Soon
Lead IC
NEI
Co-Inventors
Bharti, Kapil
ICs
NEI
Applications
Therapeutics
Research Materials
Therapeutic Areas
Ophthalmology
Development Stages
Prototype
Research Products
Human iPSC Lines
Human Cell Lines

The National Eye Institute (NEI) seeks research co-development partners and/or licensees for the development of a novel iPSC differentiation protocol for generating fibroblasts and endothelial cells.

This technology includes a novel protocol for differentiating induced pluripotent stem cells (iPSCs) into fibroblasts and endothelial cells, which are crucial for tissue engineering and regenerative medicine applications. Current methods for generating these cell types can be inefficient and inconsistent, leading to challenges in research and therapeutic applications. This protocol aims to streamline the differentiation process, enhancing the yield and quality of the derived cells.

The technical solution leverages optimized culture conditions and growth factors to promote the efficient differentiation of iPSCs into fibroblasts and endothelial cells. This is significant because it addresses the growing demand for reliable and reproducible cell sources in research and clinical settings. By providing a standardized method, this technology can facilitate advancements in tissue engineering, drug testing, and regenerative therapies.

The licensing opportunity for this technology is open to partnerships with companies and research institutions interested in cell therapy, regenerative medicine, and related fields. Collaborators can expect to engage in co-development efforts to further refine and commercialize the protocol, ensuring its applicability in various biomedical applications.

Commercial Applications
• Regenerative medicine • Tissue engineering • Drug testing and development • Cell therapy • Research in developmental biology

Competitive Advantages
• Streamlined differentiation process for iPSCs into fibroblasts and endothelial cells • High yield and quality of differentiated cells • Standardized protocol enhances reproducibility • Potential for broad applications in regenerative medicine and tissue engineering • Addresses current inefficiencies in existing methods
Licensing Contact:
Fenn, Edward (Tedd)
tedd.fenn@nih.gov