Heald A F, Ita C E, Schreiber E C
J Pharm Sci. 1976 May;65(5):768-9. doi: 10.1002/jps.2600650542.
A fluorometric method was developed for the determination of cephradine in plasma. A fluorescent product is formed when samples of deproteinized plasma containing cephradine are heated for 3 hr at 100 degrees and pH 1. The fluorescence is determined in sodium hydroxide solution (pH 13.5) at excitation and emission wavelengths of 350 and 445 nm, respectively. Only 0.1 ml of plasma is required, and concentrations of cephradine as small as 0.1 mug/ml may be determined. In plasma samples from a dog taken over a 10-hr period after an intramuscular injection of 250 mg of cephradine, essentially similar concentrations of cephradine were obtained by the fluorometric method and a standard microbiological bioassay.
已开发出一种用于测定血浆中头孢拉定的荧光法。当含有头孢拉定的脱蛋白血浆样品在100℃和pH 1的条件下加热3小时时,会形成一种荧光产物。在氢氧化钠溶液(pH 13.5)中,分别在激发波长350nm和发射波长445nm处测定荧光。仅需0.1ml血浆,即可测定低至0.1μg/ml的头孢拉定浓度。在一只狗肌肉注射250mg头孢拉定后10小时内采集的血浆样本中,荧光法和标准微生物生物测定法测得的头孢拉定浓度基本相似。