Diasio R B, Wilburn M E, Shadomy S, Espinel-Ingroff A
Antimicrob Agents Chemother. 1978 Mar;13(3):500-4. doi: 10.1128/AAC.13.3.500.
A method for the rapid, quantitative determination of 5-fluorocytosine (5-FC) in serum by high-performance liquid chromatography (HPLC) has been developed. After initially ultrafiltrating the serum, a portion was injected onto a cation exchange column. 5-FC was separated by using an ammonium-phosphate buffer as the mobile phase and detected by ultraviolet absorption at 254 nm. Quantitation of 5-FC was based on the linear relationship between peak area in the chromatograms and known concentrations of 5-FC in a set of serum standards (prepared by adding from 10 to 200 micrograms of 5-FC to 1-ml aliquots of pooled human serum). This method was compared with the standard microbiological method for 5-FC. Advantages of the HPLC method include: Determination of 5-FC levels within 30 min; lack of interference from other antimicrobial drugs, particularly amphotericin B; more accurate determination of true 5-FC level, particularly at concentrations of less than 25 micrograms/ml or greater than 100 micrograms/ml; and ease with which the assay may be automated for routine use.
已开发出一种通过高效液相色谱法(HPLC)快速、定量测定血清中5-氟胞嘧啶(5-FC)的方法。首先对血清进行超滤,然后将一部分注入阳离子交换柱。使用磷酸铵缓冲液作为流动相分离5-FC,并通过在254 nm处的紫外吸收进行检测。5-FC的定量基于色谱图中峰面积与一组血清标准品(通过向1 ml混合人血清等分试样中添加10至200微克5-FC制备)中已知浓度的5-FC之间的线性关系。将该方法与5-FC的标准微生物学方法进行了比较。HPLC方法的优点包括:在30分钟内测定5-FC水平;不受其他抗菌药物(特别是两性霉素B)的干扰;更准确地测定真实的5-FC水平,特别是在浓度低于25微克/毫升或高于100微克/毫升时;并且该测定易于自动化以用于常规使用。