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Tissue culture method in the application of preservation of articular cartilage
PAGE \* MERGEFORMAT 20
Tissue culture method in the application of preservation of articular cartilage
Authors: Song Hongjiang, Qi Jian-Hong, Yanhua Xuan, Bi Hua
Abstract [Objective] To investigate the three kinds of preservation methods on articular cartilage cell activity in the different effects to find a good effect of cartilage preservation. [Methods] harvesting adult pig cartilage, is made of about 4.5 mm × 5 mm size of the cylindrical bone cartilage. Using tissue culture method, the slow cooling gradient freezing method, the traditional slow-freezing method of cooling a continuous cartilage save processing, observe and compare the saved cartilage cell activity changes. [Results] save 8 weeks, using the traditional freezing method of the articular cartilage cell viability was less than 50%, a large number of loss of cartilage matrix components; using slow-freezing temperature gradient of cell survival rate of 66%, while the use of tissue-culture preservation of joint chondrocyte survival rate as high as 76% or more, only a small loss of cartilage matrix components. [Conclusion] compared three kinds of methods, tissue culture method can long-term preservation of articular cartilage activity is considered more desirable cartilage preservation.
Keywords: articular cartilage; preservation; tissue culture; activity
Abstract: [Objective] To study the effects of different storage method on the viability of cheodroeytes so as to find out the idem method for preservation of articular cartilage. [Method] Under the aseptic condition, acquiring 240 pieces of osteoehondral plugs from both condyles of femur and tibial plateau.The control group was not treatment using any preserved means.The tissue cultured group was to used F12 DMEM medium long term preserved osteochondral plugs under the conditions of 37 ℃. At preserve 8 weeks, takes the osteochondral section to carry on examination observation ohondrocytes Viability activeness chang
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