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关节软骨移植物的玻璃体保存。

Vitreous preservation of articular cartilage grafts.

作者信息

Song Ying C, An Yuehuei H, Kang Qian K, Li Chaoyang, Boggs Janet M, Chen Zhenzhen, Taylor Michael J, Brockbank Kelvin G M

机构信息

Charleston Research Center, Organ Recovery Systems, Charleston, South Carolina, USA.

出版信息

J Invest Surg. 2004 Mar-Apr;17(2):65-70. doi: 10.1080/08941930490422438.

Abstract

Articular cartilage has proved refractory to satisfactory cryopreservation using conventional freezing methods. Therefore, an ice-free cryopreservation method by vitrification was tested. Osteochondral plugs from New Zealand White rabbits were preserved using either a freezing method or an ice-free vitrification method of cryopreservation. Preserved and fresh control plugs were implanted in the tibial plateau of allogeneic recipients. A modified O'Driscoll grading scale, based on gross pathology, histopathology, and histochemistry, was used to evaluate the explants.The histology of fresh and vitrified explants was essentially the same, while the frozen cryopreserved explants were devoid of chondrocytes and only fibroblastlike cells were observed. The O'Driscoll grading indicated that both fresh and vitrified plugs performed significantly better than frozen plugs (p < or =.05). The results demonstrate the feasibility of vitrification as a storage method for cartilaginous tissues.

摘要

事实证明,使用传统冷冻方法对关节软骨进行令人满意的冷冻保存具有挑战性。因此,测试了一种通过玻璃化进行无冰冷冻保存的方法。采用冷冻法或无冰玻璃化冷冻保存法保存新西兰白兔的骨软骨栓。将保存的栓和新鲜对照栓植入同种异体受体的胫骨平台。基于大体病理学、组织病理学和组织化学,使用改良的奥德里斯科尔分级量表对植入物进行评估。新鲜和玻璃化植入物的组织学基本相同,而冷冻保存的植入物没有软骨细胞,仅观察到成纤维细胞样细胞。奥德里斯科尔分级表明,新鲜和玻璃化栓的表现均明显优于冷冻栓(p≤0.05)。结果证明了玻璃化作为软骨组织储存方法的可行性。

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