Granich G G, Kobayashi G S, Krogstad D J
Antimicrob Agents Chemother. 1986 Apr;29(4):584-8. doi: 10.1128/AAC.29.4.584.
We developed a rapid, sensitive, high-pressure liquid chromatographic (HPLC) procedure which incorporates a commercially available internal standard, 1-amino-4-nitronaphthalene, to measure amphotericin B in serum. Recovery was quantitative (greater than or equal to 90%), and the standard curve was linear from 0.04 to at least 10.0 micrograms/ml. The reproducibility of the assay was good, with intrarun coefficients of variation from 2.0 to 6.8% and interrun coefficients of variation from 4.9 to 10.0%. Comparison by linear regression analysis of the HPLC assay with an agar well diffusion bioassay gave a correlation coefficient of 0.942, with the HPLC assay exhibiting greater precision and sensitivity. No interference was encountered from over 20 drugs and three amphotericin B analogs. However, serum specimens that contained high concentrations of conjugated bilirubin (greater than 3 mg/dl) produced interfering peaks in both this assay and other previously reported HPLC assays for amphotericin B. We also describe a solid-phase extraction procedure which effectively removes this interference and uses an alternative internal standard (N-acetyl amphotericin B).
我们开发了一种快速、灵敏的高压液相色谱(HPLC)方法,该方法采用市售内标1-氨基-4-硝基萘来测定血清中的两性霉素B。回收率为定量(大于或等于90%),标准曲线在0.04至至少10.0微克/毫升范围内呈线性。该测定方法的重现性良好,批内变异系数为2.0%至6.8%,批间变异系数为4.9%至10.0%。通过线性回归分析将HPLC测定法与琼脂孔扩散生物测定法进行比较,相关系数为0.942,HPLC测定法表现出更高的精密度和灵敏度。超过20种药物和三种两性霉素B类似物未产生干扰。然而,含有高浓度结合胆红素(大于3毫克/分升)的血清标本在本测定法以及其他先前报道的两性霉素B的HPLC测定法中均产生干扰峰。我们还描述了一种固相萃取方法,该方法可有效消除这种干扰,并使用替代内标(N-乙酰两性霉素B)。