Van der Lee J J, Nouws J F, Bloemendal F W
J Vet Pharmacol Ther. 1982 Sep;5(3):161-75. doi: 10.1111/j.1365-2885.1982.tb00427.x.
The disposition of chloramphenicol after intramammary and intravenous administration was followed through determinations of chloramphenicol in blood and milk by means of high-performance differential pulse polarography. The concentration-time curves obtained reflected the different modes of administration, and allowed calculation of some pharmacokinetic parameters. The results of the polarographic determination in blood agreed fairly well with those of the microbiological assay in serum. Several body fluids and tissues of the cows were examined for residues of chloramphenicol and degradation products, both by the microbiological method and by high-performance liquid chromatography with ultraviolet detection. In urine, chloramphenicol and chloramphenicol glucuronide were found; in the other fluids and tissues only now and then a trace of chloramphenicol or a degradation product was detected. From these results it appears that chloramphenicol and degradation products are eliminated rapidly and completely after intravenous or intramammary application. No accumulation of degradation products occurred.
通过高效差分脉冲极谱法测定血液和乳汁中的氯霉素,跟踪乳房内给药和静脉给药后氯霉素的处置情况。所得的浓度-时间曲线反映了不同的给药方式,并可计算一些药代动力学参数。血液中极谱测定的结果与血清中微生物测定的结果相当吻合。通过微生物学方法和带有紫外检测的高效液相色谱法,对奶牛的几种体液和组织进行了氯霉素及其降解产物残留的检测。在尿液中发现了氯霉素和氯霉素葡糖醛酸;在其他体液和组织中,只是偶尔检测到微量的氯霉素或一种降解产物。从这些结果看来,静脉或乳房内给药后,氯霉素及其降解产物能迅速且完全地被消除。没有出现降解产物的蓄积。