19121 Rabbit Achilles Tendon Reconstruction with a Tissue-Engineered Silk Scaffold

Saturday, September 24, 2011: 10:20 AM
Non-Physical Computer Presentation -- Kiosks on Exhibit Floor
Su-Rak Eo, MD, PhD , Plastic and Reconstructive Surgery, Dongguk University Medical Center, GoYang-si, South Korea
Sang-Hun Cho, MD, PhD , Plastic and Reconstructive Surgery, DongGuk University Medical Center, GoYang-si, South Korea
Jun-Hyung Kim, MD , Plastic and Reconstructive Surgery, Dongguk University Medical Center, GoYang-si, South Korea
Young-Kwon Seo, PhD , Dongguk University Research Institute of Biotechnology, Dongguk University, Seoul, South Korea
Hyun-Jic Lee, MD , Plastic and Reconstructive Surgery, DongGuk University Medical Center, GoYang-si, South Korea
E-Poster
Background: The objective of the present study was to determine the feasibility and biocompatibility of a silk scaffold and of a composite silk scaffold in terms of new tendon generation using a rabbit Achilles tendon model. Methods: The silk scaffold was constructed using a weaving machine and dry-coated with collagen-hyaluronan (HA), whereas the composite silk scaffold was made by covering a silk scaffold with a lyophilized collagen-HA substrate. We implanted the tendon prostheses into Achilles tendon defects in 16 white New Zealand rabbits. We established the following three experimental groups based on the replacement substitutes used: group I (silk scaffold alone); group II (composite silk scaffold); and group III (composite silk scaffold ensheathed in a human  amniotic membrane). Implants were harvested 2, 8, and 12 weeks post-implantation. Histological examinations were conducted using hematoxylin-eosin, Masson’s trichrome, and by performing immunohistochemical staining for CD34. Tenocyteswere cultured in vitro to compare cell populations in the three groups. Results: After 8 weeks, all experimental specimens resembled normal Achilles tendons; the three groups were indistinguishable based on gross examination. The histologic examination revealed more organized collagen fibrils in groups II and III, which showed a dense, parallel, linear organization of collagen bundles. CD34 staining revealed neoangiogenesis in groups II and III. The cellular densities on composite silk scaffolds were 40% higher on average than on silk scaffolds in 30-day tenocyte cultures. Conclusions: The composite silk scaffold is a much more biocompatible tendon prosthesis than the silk scaffold. Collagen-HA substrates accelerate cellular migration and angiogenesis in neotendons.