Biocompatibility of genipin-fixed porcine aorta as a possible esophageal prosthesis

Abstract In this study, porcine aortic tissues were fixed with genipin to construct an esophageal prosthesis. In vitro characterization was performed and in vivo biocompatibility experiments were undertaken to evaluate the biological properties of genipin-fixed porcine aortic tissues. The porcine aortic tissues fixed with genipin at pH 4.0, 0.625 g/100 ml initial fixative concentrations for 7 days showed more favorable characteristics. It was characterized by low antigenicity, good epithelial cellular compatibility, favorable biomechanical properties for an esophageal prosthesis, high resistance against enzymatic degradation and be readily available. The porcine aortic tissues fixed with genipin also showed good biocompatibility in vivo. The present study demonstrated that the genipin-fixed porcine aortic tissues could be a promising material for the construction of an esophageal prosthesis or fabricating scaffold for a tissue engineered esophagus.

[1]  S. Hoerstrup,et al.  Tissue engineering in cardiovascular surgery: MTT, a rapid and reliable quantitative method to assess the optimal human cell seeding on polymeric meshes. , 1999, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

[2]  F. Mi,et al.  Characterization of ring‐opening polymerization of genipin and pH‐dependent cross‐linking reactions between chitosan and genipin , 2005 .

[3]  H. Suh,et al.  Development of collagenase-resistant collagen and its interaction with adult human dermal fibroblasts. , 2003, Biomaterials.

[4]  D. Kidron,et al.  Comparative experimental study of esophageal wall regeneration after prosthetic replacement. , 1999, Journal of biomedical materials research.

[5]  H. Sung,et al.  Genipin-crosslinked gelatin microspheres as a drug carrier for intramuscular administration: in vitro and in vivo studies. , 2003, Journal of biomedical materials research. Part A.

[6]  Y. Shimizu,et al.  Replacement of long segments of the esophagus with a collagen-silicone composite tube. , 1995, ASAIO journal.

[7]  Peifeng Liu,et al.  Synthesis and characterization of arginine–glycine–aspartic peptides conjugated poly(lactic acid-co-l-lysine) diblock copolymer , 2008, Journal of materials science. Materials in medicine.

[8]  B. Ratner,et al.  Protein bonding on biodegradable poly(L-lactide-co-caprolactone) membrane for esophageal tissue engineering. , 2006, Biomaterials.

[9]  C. Schmidt,et al.  Acellular vascular tissues: natural biomaterials for tissue repair and tissue engineering. , 2000, Biomaterials.

[10]  Tatsuo Nakamura,et al.  The experimental replacement of a cervical esophageal segment with an artificial prosthesis with the use of collagen matrix and a silicone stent. , 1998, The Journal of thoracic and cardiovascular surgery.

[11]  H. Sung,et al.  Biocompatibility study of a biological tissue fixed with a naturally occurring crosslinking reagent. , 1998, Journal of biomedical materials research.

[12]  Edgar F. Bermax The Experimental Replacement of Portions of the Esophagus by a Plastic Tube , 1952 .

[13]  H. Sung,et al.  Physical properties of a porcine internal thoracic artery fixed with an epoxy compound. , 1996, Biomaterials.

[14]  D. A. French,et al.  Use of a collagen coated vicryl tube in reconstruction of the porcine esophagus. , 1991, European journal of pediatric surgery.

[15]  M. Kitajima,et al.  A Neo-Esophagus Reconstructed by Cultured Human Esophageal Epithelial Cells, Smooth Muscle Cells, Fibroblasts, and Collagen , 2004, ASAIO journal.

[16]  Yen Chang,et al.  Construction of varying porous structures in acellular bovine pericardia as a tissue-engineering extracellular matrix. , 2005, Biomaterials.

[17]  H. Sung,et al.  Feasibility study of a natural crosslinking reagent for biological tissue fixation. , 1998, Journal of biomedical materials research.

[18]  D. Lin,et al.  Crosslinking characteristics of an epoxy-fixed porcine tendon: effects of pH, temperature, and fixative concentration. , 1996, Journal of biomedical materials research.

[19]  Yu Xi-xun,et al.  Preparation and endothelialization of decellularised vascular scaffold for tissue-engineered blood vessel , 2008 .

[20]  H. Sung,et al.  Stability of a biological tissue fixed with a naturally occurring crosslinking agent (genipin). , 2001, Journal of biomedical materials research.

[21]  Y. Hirooka,et al.  Evaluation of decellularized esophagus as a scaffold for cultured esophageal epithelial cells. , 2006, Journal of biomedical materials research. Part A.

[22]  M. Fujimaki,et al.  Experimental study of an artificial esophagus using a collagen sponge, a latissimus dorsi muscle flap, and split-thickness skin , 2010, Surgery today (Print).

[23]  V. Egorov,et al.  Mechanical properties of the human gastrointestinal tract. , 2002, Journal of biomechanics.

[24]  H. Sung,et al.  Mechanical properties of a porcine aortic valve fixed with a naturally occurring crosslinking agent. , 1999, Biomaterials.

[25]  B. Ratner,et al.  Esophageal epithelial cell interaction with synthetic and natural scaffolds for tissue engineering. , 2005, Biomaterials.

[26]  Yen Chang,et al.  Crosslinking characteristics and mechanical properties of a bovine pericardium fixed with a naturally occurring crosslinking agent. , 1999, Journal of biomedical materials research.

[27]  Yen Chang,et al.  Fixation of biological tissues with a naturally occurring crosslinking agent: fixation rate and effects of pH, temperature, and initial fixative concentration. , 2000, Journal of biomedical materials research.