Literature DB >> 10091923

In vitro evaluation of cytotoxicity of a naturally occurring cross-linking reagent for biological tissue fixation.

H W Sung1, R N Huang, L L Huang, C C Tsai.   

Abstract

A recognized drawback of the currently available chemical cross-linking reagents used to fix bioprostheses is the potential toxic effects a recipient may be exposed to from the fixed tissues and/or the residues. It is, therefore, desirable to provide a cross-linking reagent which is of low cytotoxicity and may form stable and biocompatible cross-linked products. To achieve this goal, a naturally occurring cross-linking reagent -- genipin -- which has been used in herbal medicine and in the fabrication of food dyes, was used by our group to fix biological tissues. The study was to assess the cytotoxicity of genipin in vitro using 3T3 fibroblasts (BALB/3T3 C1A31-1-1). Glutaraldehyde, the most commonly used cross-linking reagent for tissue fixation, was used as a control. The cytotoxicity of the glutaraldehyde- and genipin-fixed tissues and their residues was also evaluated and compared. The observation in the light microscopic examination revealed that the cytotoxicity of genipin was significantly lower than that of glutaraldehyde. Additionally, the results obtained in the MTT assay implied that genipin was about 10000 times less cytotoxic than glutaraldehyde. Moreover, the colony forming assay suggested that the proliferative capacity of cells after exposure to genipin was approximately 5000 times greater than that after exposure to glutaraldehyde. It was noted that the cells seeded on the surface of the glutaraldehyde-fixed tissue were not able to survive. In contrast, the surface of the genipin-fixed tissue was found to be filled with 3T3 fibroblasts. Additionally, neocollagen fibrils made by these fibroblasts were observed on the genipin-fixed tissue. This fact suggested that the cellular compatibility of the genipin-fixed tissue was superior to its glutaraldehyde-fixed counterpart. Also, the residues from the glutaraldehyde-fixed tissue markedly reduced the population of the cultured cells, while those released from the genipin-fixed tissue had no toxic effect on the seeded cells. In conclusion, as far as cytotoxicity is concerned, genipin is a promising cross-linking reagent for biological tissue fixation.

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Year:  1999        PMID: 10091923     DOI: 10.1163/156856299x00289

Source DB:  PubMed          Journal:  J Biomater Sci Polym Ed        ISSN: 0920-5063            Impact factor:   3.517


  60 in total

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Authors:  Wei-Chuan Chen; Chao-Ling Yao; Yu-Hong Wei; I-Ming Chu
Journal:  Cytotechnology       Date:  2010-10-23       Impact factor: 2.058

2.  Genipin-crosslinked chitosan/gelatin blends for biomedical applications.

Authors:  Valeria Chiono; Ettore Pulieri; Giovanni Vozzi; Gianluca Ciardelli; Arti Ahluwalia; Paolo Giusti
Journal:  J Mater Sci Mater Med       Date:  2007-08-01       Impact factor: 3.896

3.  Genipin crosslinking of cartilage enhances resistance to biochemical degradation and mechanical wear.

Authors:  Megan E McGann; Craig M Bonitsky; Mariah L Jackson; Timothy C Ovaert; Stephen B Trippel; Diane R Wagner
Journal:  J Orthop Res       Date:  2015-05-18       Impact factor: 3.494

4.  The physicochemical properties of legume protein isolates and their ability to stabilize oil-in-water emulsions with and without genipin.

Authors:  Stuart P Johnston; Michael T Nickerson; Nicholas H Low
Journal:  J Food Sci Technol       Date:  2014-11-21       Impact factor: 2.701

5.  New crosslinkers for electrospun chitosan fibre mats. I. Chemical analysis.

Authors:  Marjorie S Austero; Amalie E Donius; Ulrike G K Wegst; Caroline L Schauer
Journal:  J R Soc Interface       Date:  2012-05-23       Impact factor: 4.118

6.  Optimization of protein crosslinking formulations for the treatment of degenerative disc disease.

Authors:  Paul Slusarewicz; Keng Zhu; Bryan Kirking; Justin Toungate; Tom Hedman
Journal:  Spine (Phila Pa 1976)       Date:  2011-01-01       Impact factor: 3.468

7.  Growth factor sequestration and enzyme-mediated release from genipin-crosslinked gelatin microspheres.

Authors:  Paul A Turner; Jeffrey S Thiele; Jan P Stegemann
Journal:  J Biomater Sci Polym Ed       Date:  2017-07-20       Impact factor: 3.517

8.  Modulating In Vivo Degradation Rate of Injectable Extracellular Matrix Hydrogels.

Authors:  Jean W Wassenaar; Rebecca L Braden; Kent G Osborn; Karen L Christman
Journal:  J Mater Chem B       Date:  2016-03-28       Impact factor: 6.331

9.  Chitosan-genipin microspheres for the controlled release of drugs: clarithromycin, tramadol and heparin.

Authors:  Ruth Harris; Elena Lecumberri; Angeles Heras
Journal:  Mar Drugs       Date:  2010-05-26       Impact factor: 5.118

10.  Whole globe inflation testing of exogenously crosslinked sclera using genipin and methylglyoxal.

Authors:  Fergus F Wong; David R Lari; David S Schultz; Jay M Stewart
Journal:  Exp Eye Res       Date:  2012-08-01       Impact factor: 3.467

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