Hamel E, Johnson G, Glaubiger D
Cancer Treat Rep. 1981 Jul-Aug;65(7-8):545-53.
A rapid biochemical assay for leucovorin (LV) and N5-methyltetrahydrofolate (mTHFA) has been developed, using a cell-free extract of Escherichia coli. The reaction used was the formylation of [14C]methionyl-tRNA fMet E. coli, in which product formation is dependent on added folate derivatives. The actual formyl donor, N10-formyltetrahydrofolate, is generated from LV in the presence of ATP or from mTHFA in the presence of NAD+ or NADP+. The assay is sensitive to approximately 5 X 10(-8) M l-LV and 5 X 10(-7) M l-mTHFA in serum. There is no cross-reactivity between LV and mTHFA. The presence of methotrexate (MTX) has no effect on assay results. This assay has been used to determine LV and mTHFA levels in patients receiving LV rescue after high-dose MTX infusions. Patients received 96 mg/m2 of LV as a single iv dose at the conclusion of the MTX infusion. Serum levels of LV and mTHFA were followed for the next 6 hrs. The initial (5-min) level and LV was about 10(-5) M, and its concentration in the serum decreased rapidly. The alpha-phase half-life of LV was about 15 mins, but LV was readily detectable by the assay for 3-4 hrs. There was rapid apparent conversion to mTHFA, as this compound was also detectable at the initial time point. The level of mTHFA increased for at least 60 mins, being equimolar with LV by 30 mins, and then decreased slowly with an apparent half-life of 2-3 hrs.
利用大肠杆菌的无细胞提取物,已开发出一种用于亚叶酸(LV)和N5-甲基四氢叶酸(mTHFA)的快速生化检测方法。所使用的反应是[14C]甲硫氨酰-tRNA fMet大肠杆菌的甲酰化反应,其中产物的形成依赖于添加的叶酸衍生物。实际的甲酰供体N10-甲酰四氢叶酸,在ATP存在下由LV生成,或在NAD+或NADP+存在下由mTHFA生成。该检测方法对血清中约5×10(-8) M的l-LV和5×10(-7) M的l-mTHFA敏感。LV和mTHFA之间无交叉反应。甲氨蝶呤(MTX)的存在对检测结果无影响。该检测方法已用于测定大剂量MTX输注后接受LV解救的患者体内LV和mTHFA的水平。患者在MTX输注结束时接受96 mg/m2的LV单次静脉注射剂量。在接下来的6小时内监测血清中LV和mTHFA的水平。LV的初始(5分钟)水平约为10(-5) M,其在血清中的浓度迅速下降。LV的α相半衰期约为15分钟,但该检测方法在3 - 4小时内仍可轻易检测到LV。存在迅速向mTHFA的明显转化,因为在初始时间点也可检测到该化合物。mTHFA的水平至少在60分钟内升高,在30分钟时与LV等摩尔,然后缓慢下降,表观半衰期为2 - 3小时。