Kay A G, Rooney P, Kearney J, Pegg D E
Cryo Letters. 2015 May-Jun;36(3):187-94.
Osteochondral allografting techniques are limited by the availability of suitable donor tissue; there is an urgent need for effective cryopreservation. A fundamental requirement is the need to establish initial conditions of exposure to cryoprotectant that the chondrocytes will tolerate and that load the tissue with an adequate concentration of cryoprotectant. Three vehicle solutions to transport DMSO into the tissue were studied. Knee joints were obtained from deceased donors with appropriate consent. Whole condyles were treated with 20% w/w DMSO in each of three vehicle solutions and chondrocyte function and tissue CPA content measured. The results showed that exposure to 20% DMSO in each vehicle solution for 2 hours at 0 degrees C was tolerated without loss of GAG synthetic activity. It was observed that penetration of DMSO increased little after 1 hour of CPA exposure at 0 degrees C but the final tissue concentration of CPA was markedly lower than that in the medium.
异体骨软骨移植技术受到合适供体组织可用性的限制;迫切需要有效的冷冻保存方法。一个基本要求是需要确定软骨细胞能够耐受的接触冷冻保护剂的初始条件,并使组织中加载足够浓度的冷冻保护剂。研究了三种将二甲基亚砜(DMSO)输送到组织中的载体溶液。在获得适当同意后,从已故供体获取膝关节。将整个髁突在三种载体溶液中的每一种中用20%(重量/重量)的DMSO处理,并测量软骨细胞功能和组织中冷冻保护剂添加剂(CPA)的含量。结果表明,在0℃下于每种载体溶液中暴露于20% DMSO 2小时可被耐受,且不会丧失糖胺聚糖(GAG)合成活性。观察到在0℃下暴露于CPA 1小时后,DMSO的渗透增加很少,但最终组织中CPA的浓度明显低于培养基中的浓度。