The ability to generate predictive models linking the in vitro assessment of pharmaceutical products with in vivo performance has the potential to enable greater control of clinical quality whilst minimizing the number of in vivo studies in drug development. Artificial neural networks (ANNs) provide
In vitro and in vivo proposal of an artificial esophagus
✍ Scribed by Maurizio Marzaro; Simonetta Vigolo; Barbara Oselladore; Maria Teresa Conconi; Domenico Ribatti; Stefano Giuliani; Beatrice Nico; Giampiero Perrino; Gastone Giovanni Nussdorfer; Pier Paolo Parnigotto
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 640 KB
- Volume
- 77A
- Category
- Article
- ISSN
- 1549-3296
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Artificial materials and autologous tissues used for esophageal reconstruction often induce complications like stenosis and leakage at long‐term follow‐up. This study evaluates the possibility to obtain in vitro an implantable tissue‐engineered esophagus composed of homologous esophageal acellular matrix and autologous smooth muscle cells (SMCs). Acellular matrices obtained by detergent‐enzymatic method did not present any major histocompatibility complex marker and expressed bFGF as protein, showing angiogenic activity in vivo on the chick embryo chorioallantoic membrane (CAM). Moreover, they supported cell adhesion, and inasmuch as just after 24 h from seeding, the scaffold appeared completely covered by SMCs. To verify the biocompatibility of our constructs, defects created in the porcine esophageal wall were covered using homologous acellular matrices with and without cultures of autologous SMCs. At 3 week from surgery, the patches composed of only acellular matrices showed a more severe inflammatory response and were negative for α‐smooth muscle actin immunostaining. In contrast, the cell‐matrix implants presented ingrowth of SMCs, showing an early organization into small fascicules. Collectively, these results suggest that patches composed of homologous esophageal acellular matrix and autologous SMCs may represent a promising tissue‐engineering approach for the repair of esophageal injuries. © 2006 Wiley Periodicals, Inc. J Biomed Mater Res, 2006
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