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Active NON-SBIR/STTR RPGS NIH (US)

Engineering biomimetic 3D printed urethral tissue constructs using elastin-based bioinks for urethroplasty

$1.77M USD

Funder NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING
Recipient Organization University of California Los Angeles
Country United States
Start Date Sep 01, 2024
End Date May 31, 2026
Duration 637 days
Number of Grantees 2
Roles Principal Investigator; Co-Investigator
Data Source NIH (US)
Grant ID 10989436
Grant Description

Project Summary Urethral defects requiring urethroplasty occur in children and adults secondary to congenital, traumatic, infectious, and malignant conditions. Current tissue sources for urethral replacement are limited by donor site morbidity and lack of optimal tissue characteristics to support lifelong voiding and penile erections. A subsequent

high risk of short- and long-term urethroplasty complications highlights the need for an improved tissue alternative with a bioinspired design. The goal of this proposal is to engineer highly elastic, biomimetic, three dimensional (3D) bioprinted multi-layered urethral tissue constructs by combining novel bioinks,

made of a human protein and decellularized matrix, with an innovative 3D bioprinting strategy. This research plan addresses key design requirements: 1) achieving target elasticity by layer in a suturable construct, 2) incorporating critical biological cues to enhance wound healing and vascularization, and 3) applying a 3D

bioprinting technique to create optimized properties by layer with a recapitulation of the native urethral layered structure. Our overall hypothesis is that these novel 3D bioprinted constructs made from methacrylate human recombinant tropoelastin (MeTro), a photocrosslinkable human-based elastomeric hydrogel, and bladder

decellularized matrix (BAM), that are designed to meet targeted mechanical and 3D structural parameters will improve suturability, early urinary tract function, and local tissue regeneration as compared to unseeded scaffold urethroplasties. In Aim 1, MeTro and BAM bioinks with mechanical and structural properties that mimic native

urethral tissue will be engineered. Then, the designed bioinks will be 3D bioprinted to form cell-laden bi-layered patch constructs containing two primary lower urinary tract cell lines: urothelium and smooth muscle cells. In Aim 2, the in vivo efficacy of the engineered cell-laden MeTro/BAM bioprinted constructs, in seeded and

unseeded configurations, will be applied to a rat patch urethroplasty model, investigating biologic and functional outcome parameters. Put together, this research strategy will engineer finely tuned elastic 3D printed biomimetic constructs with target mechanical and 3D structural parameters derived from urethral tissue analyses to

maximize future clinical translatability.

All Grantees

University of California Los Angeles

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