Daene A, Holle M, Stolle K, Weissflog A, Ehrenberg M, Thierbach V, Grützmann H, Coutelle C, Roigas H, Rosenthal S
Acta Biol Med Ger. 1977;36(3-4):425-32.
The cryoprotective effect of dimethylsulfoxide, glycerol and polyethylenglycol during freezing and thawing of human bone marrow was investigated by eosin staining test, an acridinorange fluochrome staining test and by RNA- and DNA-synthesis tests. In these tests the overall yield of vital nucleated cells, referred to the number in the absence of cryoprotectants and freezing and thawing, amounted to 50% with dimethylsulfoxide, 30% with glycerol, and 10% with polyethylenglycol. With dimethylsulfoxide and glycerol the loss of vital nucleated cells is almost entirely due to the addition of cryoprotectants. Polyethylenglycol freezing and thawing also leads to a great loss of vital nucleated cells. The results with dimethylsulfoxide show that the currently employed techniques of punction, preparation, freezing and thawing of bone marrow are suitable for clinical application.
通过伊红染色试验、吖啶橙荧光染色试验以及RNA和DNA合成试验,研究了二甲基亚砜、甘油和聚乙二醇在人骨髓冻融过程中的冷冻保护作用。在这些试验中,与不存在冷冻保护剂以及冻融情况下的细胞数量相比,有活力的有核细胞的总产量,使用二甲基亚砜时为50%,使用甘油时为30%,使用聚乙二醇时为10%。使用二甲基亚砜和甘油时,有活力的有核细胞的损失几乎完全是由于添加了冷冻保护剂。聚乙二醇冻融也会导致大量有活力的有核细胞损失。二甲基亚砜的试验结果表明,目前采用的骨髓穿刺、制备、冷冻和解冻技术适用于临床应用。