Boon M E, Schmidt U, Cramer-Knijnenburg G I, van Krieken J H
Leiden Cytology and Pathology Laboratory, The Netherlands.
Pathol Res Pract. 1992 Oct;188(7):832-5. doi: 10.1016/S0344-0338(11)80240-2.
Although used for over one century formalin has several disadvantages which Kryofix, an alternative fixative for paraffin blocks used in Leiden for 6 years, does not have. In this study the effects of Kryofix on tissue regarding immunohistochemistry are compared with those of buffered formalin. All markers studied showed enhanced staining in the Kryofix blocks after 4 hours of fixation, whilst in some cases the immunostaining of the formalin blocks was even negative. For all markers, the sera could be further diluted for the Kryofix sections, for some with as much as a factor 20, enhancing the cost-effectiveness of the method. We established that for formalin, the fixation time strongly influenced the results. For Kryofix there was no time factor: the immunostaining results of 1 hour fixation were identical to those after 3 months of fixation. This study shows that by this method of fixation, in which there is no cross-linking of proteins, immunostaining of paraffin sections is optimized and standardized.
尽管福尔马林已使用了一个多世纪,但它有几个缺点,而在莱顿使用了6年的石蜡块替代固定剂Kryofix则没有这些缺点。在本研究中,将Kryofix对组织免疫组化的影响与缓冲福尔马林的影响进行了比较。所有研究的标志物在固定4小时后,Kryofix包埋块中的染色均增强,而在某些情况下,福尔马林包埋块的免疫染色甚至呈阴性。对于所有标志物,Kryofix切片的血清可进一步稀释,有些可稀释多达20倍,从而提高了该方法的成本效益。我们发现,对于福尔马林,固定时间对结果有很大影响。对于Kryofix,不存在时间因素:1小时固定的免疫染色结果与3个月固定后的结果相同。本研究表明,通过这种不存在蛋白质交联的固定方法,石蜡切片的免疫染色得以优化和标准化。