A 3-dimensional bioprinted tracheal segment implant pilot study: Rabbit tracheal resection with graft implantation

• Published in: International journal of pediatric otorhinolaryngology 2019-02, Vol.117, p.175-178
• Main Authors: Kaye, Rachel, Goldstein, Todd, Grande, Daniel A., Zeltsman, David, Smith, Lee P.
• Format: Article
• Language: English
• Subjects: Airway reconstruction; Bioprinting; Three dimensional printing; Tracheal graft; Tracheal implant; Tracheal resection
• ISSN: 0165-5876; 1872-8464
• DOI: 10.1016/j.ijporl.2018.11.010

Surgical reconstruction of tracheal disease has expanded to include bioengineering and three dimensional (3D) printing. This pilot study investigates the viability of introducing a living functional tracheal replacement graft in a rabbit animal model. Seven New Zealand White rabbits were enrolled and six completed participation (one intraoperative mortality). Tracheal replacement grafts were created by impregnating 3D printed biodegradable polycaprolactone (PCL) tracheal scaffolds with rabbit tracheal hyaline chondrocytes. 2 cm of native trachea was resected and the tracheal replacement graft implanted. Subjects were divided into two equal groups (n = 3) that differed in their time of harvest following implantation (three or six weeks). Tracheal specimens were analyzed with intraluminal telescopic visualization and histopathology. The two groups did not significantly differ in histopathology or intraluminal diameter. All sections wherein the implant telescoped over native trachea (anastomotic ends) contained adequate hyaline cartilage formation (i.e. chondrocytes within lacuna, surrounding extracellular matrix, and strong Safranin O staining). Furthermore, the PCL scaffold was surrounded by a thin layer of fibrous tissue. All areas without membranous coverage contained inadequate or immature cartilage formation with inflammation. The average intraluminal stenosis was 83.4% (range 34.2–95%). We report normal cartilage growth in a tracheal replacement graft when chondrocytes are separated from the tracheal lumen by an intervening membrane. When no such membrane exists there is a propensity for inflammation and stenosis. These findings are important for future construction and implantation of tracheal replacement grafts. Not applicable: this is an in vivo animal trial.