1. Spitz, L. Esophageal atresia. J. Pediatr. Surg.41, 1635–1640 (2006).
2. Londono, R. & Badylak, S. F. Regenerative Medicine Strategies for Esophageal Repair. Tissue Eng. Part B Rev.21, 393–410 (2015).
3. Langer, R. & Vacanti, J. Tissue engineering. Science (80-. ).260, 920–926 (1993).
4. Vacanti, J. P. & Langer, R. Tissue engineering: the design and fabrication of living replacement devices for surgical reconstruction and transplantation. Lancet354, S32–S34 (1999).
5. Hasirci, V. & Hasirci, N. Fundamentals of Biomaterials. (Springer New York, 2018). doi:10.1007/978-1-4939-8856-3.
6. Kunisaki, S. M. & Coran, A. G. Esophageal replacement. Semin. Pediatr. Surg.26, 105–115 (2017).
7. Lee, S.-E., Massie, I., Meran, L. & Li, V. S. W. Extracellular Matrix Remodeling in Intestinal Homeostasis and Disease. in 99–140 (2018). doi:10.1016/bs.asn.2018.01.001.
8. Keane, T. J., Horejs, C.-M. & Stevens, M. M. Scarring vs. functional healing: Matrix-based strategies to regulate tissue repair. Adv. Drug Deliv. Rev.129, 407–419 (2018).
9. Bilgic, H. et al. Gelatin Based Scaffolds and Effect of EGF Dose on Wound Healing. J. Biomater. Tissue Eng.3, 205–211 (2013).
10. Isikli, C. & Hasirci, N. Surface and Cell Affinity Properties of Chitosan-Gelatin-Hydroxyapatite Composite Films. Key Eng. Mater.493–494, 337–342 (2011).
11. Malikmammadov, E., Tanir, T. E., Kiziltay, A. & Hasirci, N. Preparation and characterization of poly(ε-caprolactone) scaffolds modified with cell-loaded fibrin gel. Int. J. Biol. Macromol.125, 683–689 (2019).
12. Ulubayram, K., Aksu, E., Gurhan, S. I. D., Serbetci, K. & Hasirci, N. Cytotoxicity evaluation of gelatin sponges prepared with different cross-linking agents. J. Biomater. Sci. Polym. Ed.13, 1203–1219 (2002).
13. Bahcecioglu, G., Buyuksungur, A., Kiziltay, A., Hasirci, N. & Hasirci, V. Construction and in vitro testing of a multilayered, tissue-engineered meniscus. J. Bioact. Compat. Polym.29, 235–253 (2014).
14. Subbiah, R. & Guldberg, R. E. Materials Science and Design Principles of Growth Factor Delivery Systems in Tissue Engineering and Regenerative Medicine. Adv. Healthc. Mater.8, 1801000 (2019).
15. Guler, F. et al. The effects of local and sustained release of fibroblast growth factor on testicular blood flow and morphology in spermatic artery— and vein-ligated rats. J. Pediatr. Surg.39, 709–716 (2004).
16. Sakallioglu, A. E. et al. Sustained local application of low-dose epidermal growth factor on steroid-inhibited colonic wound healing. J. Pediatr. Surg.39, 591–595 (2004).
17. Bingol-Kologlu, M. et al. Effects of Local and Sustained Release of FGF, IGF, and GH on Germ Cells in Unilateral Undescended Testis in Rats. Urology75, 223–228 (2010).
18. Fedakar-Senyucel, M. et al. The effects of local and sustained release of fibroblast growth factor on wound healing in esophageal anastomoses. J. Pediatr. Surg.43, 290–295 (2008).
19. Ulubayram, K. EGF containing gelatin-based wound dressings. Biomaterials22, 1345–1356 (2001).
20. Karakayali, F. et al. Evaluation of Neointimal Hyperplasia on Tranilast-Coated Synthetic Vascular Grafts: An Experimental Study. J. Investig. Surg.20, 167–173 (2007).
21. Houchen, C. W., George, R. J., Sturmoski, M. A. & Cohn, S. M. FGF-2 enhances intestinal stem cell survival and its expression is induced after radiation injury. Am. J. Physiol. Liver Physiol.276, G249–G258 (1999).
22. Tabata, Y. The importance of drug delivery systems in tissue engineering. Pharm. Sci. Technolo. Today3, 80–89 (2000).
23. Kilic Bektas, C. & Hasirci, V. Mimicking corneal stroma using keratocyte‐loaded photopolymerizable methacrylated gelatin hydrogels. J. Tissue Eng. Regen. Med.12, e1899–e1910 (2018).
24. Maghsoudlou, P., Eaton, S. & De Coppi, P. Tissue engineering of the esophagus. Semin. Pediatr. Surg.23, 127–134 (2014).
25. Saxena, A. Esophagus Tissue Engineering: Designing and Crafting the Components for the “Hybrid Construct” Approach. Eur. J. Pediatr. Surg.24, 246–262 (2014).
26. Kim, M. S. et al. Influence of Biomimetic Materials on Cell Migration. in 93–107 (2018). doi:10.1007/978-981-13-0445-3_6.
27. Mansilla, E. et al. Outstanding Survival and Regeneration Process by the Use of Intelligent Acellular Dermal Matrices and Mesenchymal Stem Cells in a Burn Pig Model. Transplant. Proc.42, 4275–4278 (2010).
28. Poghosyan, T. et al. Esophageal tissue engineering: Current status and perspectives. J. Visc. Surg.153, 21–29 (2016).
29. Sezer, U. A., Aksoy, E. A., Hasirci, V. & Hasirci, N. Poly(ε-caprolactone) composites containing gentamicin-loaded β-tricalcium phosphate/gelatin microspheres as bone tissue supports. J. Appl. Polym. Sci.127, 2132–2139 (2013).
30. Güney, A. & Hasirci, N. Properties and phase segregation of crosslinked PCL-based polyurethanes. J. Appl. Polym. Sci.131, n/a-n/a (2014).
31. Malikmammadov, E., Tanir, T. E., Kiziltay, A., Hasirci, V. & Hasirci, N. PCL and PCL-based materials in biomedical applications. J. Biomater. Sci. Polym. Ed.29, 863–893 (2018).
32. Koh, H. S., Yong, T., Chan, C. K. & Ramakrishna, S. Enhancement of neurite outgrowth using nano-structured scaffolds coupled with laminin. Biomaterials29, 3574–3582 (2008).
33. Bahcecioglu, G., Hasirci, N., Bilgen, B. & Hasirci, V. A 3D printed PCL/hydrogel construct with zone-specific biochemical composition mimicking that of the meniscus. Biofabrication11, 025002 (2019).
34. Tabata, Y., Hijikata, S. & Ikada, Y. Enhanced vascularization and tissue granulation by basic fibroblast growth factor impregnated in gelatin hydrogels. J. Control. Release31, 189–199 (1994).
35. Kuppan, P., Sethuraman, S. & Krishnan, U. M. PCL and PCL-Gelatin Nanofibers as Esophageal Tissue Scaffolds: Optimization, Characterization and Cell-Matrix Interactions. J. Biomed. Nanotechnol.9, 1540–1555 (2013).
36. Abramov, Y. et al. Histologic characterization of vaginal vs. abdominal surgical wound healing in a rabbit model. Wound Repair Regen.15, 80–86 (2007).
37. Zhu, Y., Zhou, M. & Hou, R. Tissue Engineering of Esophagus. in Esophageal Abnormalities (InTech, 2017). doi:10.5772/intechopen.69350.
38. Tabata, Y., Hijikata, S., Muniruzzaman, M. & Ikada, Y. Neovascularization effect of biodegradable gelatin microspheres incorporating basic fibroblast growth factor. J. Biomater. Sci. Polym. Ed.10, 79–94 (1999).
39. Liu, S. et al. Current applications of poly(lactic acid) composites in tissue engineering and drug delivery. Compos. Part B Eng.199, 108238 (2020).
40. Selcan Gungor-Ozkerim, P., Balkan, T., Kose, G. T., Sezai Sarac, A. & Kok, F. N. Incorporation of growth factor loaded microspheres into polymeric electrospun nanofibers for tissue engineering applications. J. Biomed. Mater. Res. Part A102, 1897–1908 (2014).
41. Lynen Jansen, P. et al. Surgical Mesh as a Scaffold for Tissue Regeneration in the Esophagus. Eur. Surg. Res.36, 104–111 (2004).
42. Diemer, P., Markoew, S., Le, D. Q. S. & Qvist, N. Poly-ε-caprolactone mesh as a scaffold for in vivo tissue engineering in rabbit esophagus. Dis. Esophagus28, 240–245 (2015).
43. Adam, A. B., Özdamar, M. Y., Esen, H. H. & Günel, E. Local effects of epidermal growth factor on the wound healing in esophageal anastomosis: An experimental study. Int. J. Pediatr. Otorhinolaryngol.99, 8–12 (2017).