Gilois C R, Stone J, Lai A P, Wierzbicki A S
Department of Haematology, National Hospitals for Nervous Diseases, London, England.
J Clin Pathol. 1990 Feb;43(2):160-2. doi: 10.1136/jcp.43.2.160.
The effects of varying the method of preparation of haemolysates on the measurement of red cell folate concentration were investigated using the Simultrac kit. The concentration of ascorbic acid did not have any significant effect on the assayed concentrations of folate, but lower concentrations were obtained when the incubation time was increased. Folate was stable for 14 days in cells when they were stored at 4 degrees C and for seven days at -25 degrees C, but instability was increased by storage in ascorbic acid, by the use of stored (4 degrees C) ascorbic acid, and by preparing the haemolysates by freeze-thaw cycling. It is recommended that haemolysates should be diluted in fresh ascorbic acid, at a concentration of 10 g/l, incubated for 60 minutes in the dark and stored at -20 degrees/25 degrees C before being assayed.
使用Simultrac试剂盒研究了改变溶血产物制备方法对红细胞叶酸浓度测量的影响。抗坏血酸的浓度对叶酸的测定浓度没有任何显著影响,但孵育时间增加时会得到较低的浓度。当细胞在4℃储存时,叶酸在细胞中稳定14天,在-25℃稳定7天,但在抗坏血酸中储存、使用储存(4℃)的抗坏血酸以及通过冻融循环制备溶血产物会增加其不稳定性。建议溶血产物应在浓度为10 g/l的新鲜抗坏血酸中稀释,在黑暗中孵育60分钟,并在-20℃/25℃储存后再进行测定。