Gatley S J, Brown S G, Thompson C M
Franklin McLean Institute, University of Chicago, IL 60637.
J Nucl Med. 1988 Aug;29(8):1443-7.
A rapid enzymatic method for determining the purity of 2FDG preparations has been devised. A small aliquot of the preparation is incubated with a hexokinase/adenosine triphosphate/Mg+2 mixture and passed through a Dowex 1 ion-exchange column, which retains the 2FDG-6-phosphate. Another aliquot, without prior incubation, is passed through an identical column and the 2FDG radioactivity is found in the eluant. The criteria for purity are quantitative retention of the 2FDG-6-phosphate on the column and no retention of 2FDG. Comparison of the HK method with thin layer and high performance liquid chromatography assays indicate that the HK method can serve as a rapid, simple and inexpensive alternative to these other methods. It can be used in a routine quality control program and may be easily adaptable to automated 2FDG synthetic methods.
已设计出一种快速酶法来测定2FDG制剂的纯度。取一小份制剂与己糖激酶/三磷酸腺苷/Mg+2混合物一起孵育,然后通过Dowex 1离子交换柱,该柱会保留2FDG-6-磷酸。另一份未经预先孵育的等分试样通过相同的柱,在洗脱液中发现2FDG放射性。纯度标准是2FDG-6-磷酸在柱上的定量保留以及2FDG无保留。HK法与薄层色谱法和高效液相色谱法测定结果的比较表明,HK法可作为这些其他方法的快速、简单且廉价的替代方法。它可用于常规质量控制程序,并且可能很容易适用于自动化的2FDG合成方法。