Crosslinking of biological tissues using genipin and/or carbodiimide.

The study was to investigate the crosslinking characteristics, mechanical properties, and resistance against enzymatic degradation of biological tissues after fixation with genipin (a naturally occurring crosslinking agent) and/or carbodiimide. Fresh tissue was used as a control. It was found that both genipin and carbodiimide are effective crosslinking agents for tissue fixation and genipin crosslinking is comparatively slower than carbodiimide crosslinking. Additionally, tissue fixation in genipin and/or carbodiimide may produce distinct crosslinking structures. Carbodiimide may form intrahelical and interhelical crosslinks within or between tropocollagen molecules, whereas genipin may further introduce intermicrofibrillar crosslinks between adjacent collagen microfibrils. The stability (denaturation temperature and resistance against enzymatic degradation) of the fixed tissue is mainly determined by its intrahelical and interhelical crosslinks. In contrast, intermicrofibrillar crosslinks significantly affect the mechanical properties (tissue shrinkage during fixation, tensile strength, strain at break, and ruptured pattern) of the fixed tissue. Moreover, the degree of enzymatic degradation of the fixed tissue may be influenced by three factors: the availability, to the enzyme, of recognizable cleavage sites, the degree of crosslinking, and the extent of helical integrity of tropocollagen molecules in tissue.

[1]  I. Dardik,et al.  Evaluation of glutaraldehyde-tanned human umbilical cord vein as a vascular prosthesis for bypass to the popliteal, tibial, and peroneal arteries. , 1978, Surgery.

[2]  J. Feijen,et al.  In vitro degradation of dermal sheep collagen cross-linked using a water-soluble carbodiimide. , 1996, Biomaterials.

[3]  C. A. Pereira,et al.  A multi-sample denaturation temperature tester for collagenous biomaterials. , 1995, Medical engineering & physics.

[4]  I. Gallo,et al.  Late clinical results with the use of heterologous pericardium for closure of the pericardial cavity. , 1985, The Journal of thoracic and cardiovascular surgery.

[5]  J. Kumada,et al.  The continuous hydrolysis of geniposide to genipin using immobilized β-glucosidase on calcium alginate gel , 1987, Biotechnology Letters.

[6]  T. Iwashita,et al.  Structure of genipocyanin G1, a spontaneous reaction product between genipin and glycine , 1987 .

[7]  Y. Takeda,et al.  Studies on the Blue Pigments Produced from Genipin and Methylamine. II .On the Formation Mechanisms of Brownish-Red Intermediates Leading to the Blue Pigment Formation , 1994 .

[8]  H. Sung,et al.  Degradation potential of biological tissues fixed with various fixatives: an in vitro study. , 1997, Journal of biomedical materials research.

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

[10]  Lee Jm,et al.  The bovine pericardial xenograft: I. Effect of fixation in aldehydes without constraint on the tensile viscoelastic properties of bovine pericardium , 1989 .

[11]  D E Koshland,et al.  A method for the quantitative modification and estimation of carboxylic acid groups in proteins. , 1967, The Journal of biological chemistry.

[12]  L Robert,et al.  Biological factors affecting long-term results of valvular heterografts. , 1969, The Journal of thoracic and cardiovascular surgery.

[13]  D. Simionescu,et al.  Mapping of glutaraldehyde-treated bovine pericardium and tissue selection for bioprosthetic heart valves. , 1993, Journal of biomedical materials research.

[14]  H. Sung,et al.  Reconstruction of the right ventricular outflow tract with a bovine jugular vein graft fixed with a naturally occurring crosslinking agent (genipin) in a canine model. , 2001, The Journal of thoracic and cardiovascular surgery.

[15]  A. Berger,et al.  The hydrolysis of poly (L‐prolyl‐glycyl‐L‐prolyl) by bacterial collagenase , 1972, Biopolymers.

[16]  D. A. French,et al.  Cellular invasion and breakdown of three different collagen films in the lumbar muscle of the rat. , 1990, Biomaterials.

[17]  P. Lawford,et al.  Pericardial heterografts. Toward quality control of the mechanical properties of glutaraldehyde-fixed leaflets. , 1986, The Journal of thoracic and cardiovascular surgery.

[18]  J. Feijen,et al.  Successive epoxy and carbodiimide cross-linking of dermal sheep collagen. , 1999, Biomaterials.

[19]  J. Gergely,et al.  Zero-length crosslinking procedure with the use of active esters. , 1990, Analytical biochemistry.

[20]  H Harasaki,et al.  Biomaterial-associated calcification: pathology, mechanisms, and strategies for prevention. , 1988, Journal of biomedical materials research.

[21]  J. Gillquist,et al.  Failure of a bovine xenograft for reconstruction of the anterior cruciate ligament. , 1989, Acta orthopaedica Scandinavica.

[22]  H. Sung,et al.  In vitro evaluation of cytotoxicity of a naturally occurring cross-linking reagent for biological tissue fixation. , 1999, Journal of biomaterials science. Polymer edition.

[23]  T.-H. Tsm,et al.  Identification and Determination of Geniposide, Genipin, Gardenoside, and Geniposidic Acid from Herbs by HPLC/Photodiode-Array Detection , 1994 .

[24]  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.

[25]  R. Timkovich Detection of the stable addition of carbodiimide to proteins. , 1977, Analytical biochemistry.

[26]  P. Cipriano,et al.  Calcification of Porcine Prosthetic Heart Valves: A Radiographic and Light Microscopic Study , 1982, Circulation.

[27]  J. Feijen,et al.  Cross-linking of dermal sheep collagen using a water-soluble carbodiimide. , 1996, Biomaterials.

[28]  D. A. French,et al.  Assessment of collagen film for use in urinary tract surgery. , 1986, British Journal of Urology.

[29]  H. Sung,et al.  In vitro evaluation of the genotoxicity of a naturally occurring crosslinking agent (genipin) for biologic tissue fixation. , 2000, Journal of biomedical materials research.

[30]  H. Koyanagi,et al.  Epoxy Compounds As a New Cross‐Linking Agent for Porcine Aortic Leaflets: Subcutaneous Implant Studies in Rats , 1989, Journal of cardiac surgery.

[31]  E. Wiley,et al.  Differential scanning calorimeter studies of the thermal transitions of collagen. Implications on structure and stability. , 1972, The Journal of biological chemistry.

[32]  I A Silver,et al.  Microelectrode studies on the acid microenvironment beneath adherent macrophages and osteoclasts. , 1988, Experimental cell research.

[33]  Y. Takeda,et al.  Studies on the Blue Pigments Produced from Genipin and Methylamine. I. Structures of the Brownish-Red Pigments, Intermediates Leading to the Blue Pigments , 1994 .