Kanazawa Y, Kuramata T, Matsumoto K
Jpn J Antibiot. 1982 Jul;35(7):1722-9.
Susceptibilities of 189 strains of 28 bacterial species to cephradine were determined by the 2-fold agar dilution method in parallel with the diameter of inhibition zone by the single-disc method, under the experimental condition established by Kanazawa. The experiments demonstrated significant correlation between MIC by the dilution method and diameter of inhibition zone in each of conventional assay of the over-night (about 16 hours) incubation, delayed assay (about 24 hours incubation), and rapid assay (after 3-4 or 5-6 hours incubation), thus confirming applicability of the single-disc assay for cephradine. Analysis of the data obtained by using cephradine disc containing 30 micrograms revealed the primary regression equation to be: D (diameter, mm) = 28.5-11.2 log MIC (microgram/ml) in conventional assay, D = 35.1-14.6 log MIC (microgram/ml) in delayed assay, D = 18.0-5.41 log MIC (microgram/ml) in 3-4 hours rapid assay and D = 23.2-8.33 log MIC (microgram/ml) in 5-6 6 hours rapid assay, respectively. The range of variations in MICs estimated from the diameter of of inhibition zone by the disc test was then calculated in comparison with that in MIC determined by the 2-fold agar dilution assays, as reference for the experimental errors which may be involved in the estimation of MIC of cephradine by the single-disc assay.
按照金泽建立的实验条件,采用2倍琼脂稀释法测定了28种细菌的189株菌株对头孢拉定的敏感性,并同时采用单纸片法测定抑菌圈直径。实验表明,在过夜(约16小时)培养的常规测定、延迟测定(约24小时培养)和快速测定(3 - 4或5 - 6小时培养后)中,稀释法测定的最低抑菌浓度(MIC)与抑菌圈直径之间均存在显著相关性,从而证实了单纸片法对头孢拉定的适用性。对含30微克头孢拉定纸片所得数据的分析显示,常规测定中的一级回归方程为:D(直径,mm)= 28.5 - 11.2 log MIC(微克/毫升),延迟测定中为D = 35.1 - 14.6 log MIC(微克/毫升),3 - 4小时快速测定中为D = 18.0 - 5.41 log MIC(微克/毫升),5 - 6小时快速测定中为D = 23.2 - 8.33 log MIC(微克/毫升)。然后,通过纸片试验抑菌圈直径估算的MIC变化范围与2倍琼脂稀释法测定的MIC变化范围进行比较,作为单纸片法估算头孢拉定MIC时可能涉及的实验误差参考。