Arnoczky S P, McDevitt C A, Schmidt M B, Mow V C, Warren R F
Laboratory of Comparative Orthopaedics, Hospital for Special Surgery, New York, NY 10021.
J Orthop Res. 1988;6(1):1-12. doi: 10.1002/jor.1100060102.
This study evaluated the effect of cryopreservation on the structural organization, biosynthetic activity, and material properties of canine menisci. The menisci were cryopreserved by incubating them in a 4% solution of dimethyl sulfoxide (DMSO) in physiologic media and freezing them to -100 degrees C using a controlled rate freezing system. The menisci were then stored for varying periods of time from zero to 12 weeks in liquid nitrogen (-196 degrees C). Following rapid thawing, changes in the histological appearance and biosynthetic activity of the menisci were evaluated as functions of storage time. In addition, the effects of the cryopreservation process on the tensile strength and modulus of the meniscal tissue were assessed. Although cryopreservation and short-term storage did not appear to affect the morphological appearance or biomechanical character of the menisci, biosynthetic activity, as determined by Na2S35SO4 incorporation, was diminished to less than 50% of normal control values immediately following cryopreservation and thawing. Autoradiographic examination of these tissues revealed that only approximately 10% of the meniscal cells were metabolically active, however, indicating that a marked increase in the metabolic activity of individual cells occurs following the freeze-thaw cycle. Total metabolic activity continued to decline with storage time.
本研究评估了冷冻保存对犬半月板的结构组织、生物合成活性及材料特性的影响。半月板通过在生理介质中的4%二甲亚砜(DMSO)溶液中孵育并使用控速冷冻系统将其冷冻至-100℃进行冷冻保存。然后将半月板在液氮(-196℃)中保存从零至12周不等的时间。快速解冻后,评估半月板组织学外观和生物合成活性随保存时间的变化。此外,评估了冷冻保存过程对半月板组织拉伸强度和模量的影响。尽管冷冻保存和短期储存似乎并未影响半月板的形态外观或生物力学特性,但通过掺入Na2S35SO4测定的生物合成活性在冷冻保存和解冻后立即降至正常对照值的50%以下。对这些组织的放射自显影检查显示,然而,仅有约10%的半月板细胞具有代谢活性,这表明在冻融循环后单个细胞的代谢活性显著增加。总代谢活性随保存时间持续下降。