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Active NON-SBIR/STTR RPGS NIH (US)

Nanofiber Patch with Gradient Presentation of Biomolecules for Treatment of Pediatric Tracheal Stenosis

$1.54M USD

Funder EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT
Recipient Organization Colorado State University
Country United States
Start Date Sep 01, 2024
End Date Aug 31, 2026
Duration 729 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10989143
Grant Description

PROJECT SUMMARY The long-term objective of this application is to bring a trachea patch to the market for treatment of pediatric tracheal stenosis, or narrowing of the airway, which left untreated can be a life-threatening condition. Currently, otolaryngologists have only two major options for treating tracheal stenosis. One is a complex surgical procedure

known as slide tracheoplasty that few surgeons in the country are qualified to perform. The other is to cut and splay the trachea holding it open using a graft of rib cartilage. Both are difficult, time-consuming procedures with potential complications. We have an issued U.S. patent on the trachea patch biomaterial that overcomes the five

major technical hurdles required to replace rib cartilage grafting: 1) mechanical integrity, 2) suturable, 3) resorbable, 4) air-tight, and 5) off-the-shelf. There is currently nothing on the market remotely resembling the idea of a synthetic patch for tracheal stenosis. While the academic tissue engineering community has focused

primarily on regenerating an entire trachea with highly complex strategies, arguably leading to technology in search of an application, we have focused instead on identifying a specific patient indication with an unmet need and designed a technology to fill that void. The overall hypothesis is that mimicking the wound healing environment using reinforced electrospun

scaffolds with gradient presentation of biological factors will maintain tracheal patency and regenerate cartilage- like tissue comparable to healthy tracheas. Two specific aims are proposed to determine the most attractive growth factor loading for mimicking specific stages of wound healing. Aim 1 will refine growth factor loading by

evaluating multiple compositions in a subcutaneous model. The final device composition will then be evaluated in a capstone in vivo rabbit tracheal defect study in Aim 2. Compared to rib cartilage grafting, our trachea patch holds the following advantages: 1) No surgery to remove rib tissue, saving operating room time and cost, and eliminating potential complication/infection and morbidity at

the rib site (attractive to patients and insurance companies), 2) Easy to use, as it is “plug and play” for surgeons who perform rib cartilage grafting (attractive to surgeons), 3) The gradient design has the potential to improve functionality and accelerate regeneration, promoting vascularization, macrophage recruitment, and directed

matrix synthesis. For several reasons, we focus initial clinical translation on the pediatric population with laryngotracheal stenosis. In the simplest terms, our goal is to fix tracheas for young children around the world with narrowed airways to help them survive and breathe normally again.

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Colorado State University

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