Nilsson-Ehle I, Nilsson-Ehle P
Clin Chem. 1978 Feb;24(2):365-7.
We describe a procedure for determining cefuroxime concentrations in serum by using high-performance liquid chromatography. The drug is extracted from serum with dimethylformamide and separated from other substances in the extract by reversed-phase chromatography. The ultraviolet (280-nm) absorption of the effluent was monitored and quantitated based on the height of the cefuroxime peak. Intra-and inter-assay imprecision (cv) was less than 3.1 and 4.3%, respectively. Serum concentrations as low as 1.0 mg/liter could be accurately measured. No interference from various other drugs and antibiotics was found. A biological half-life of 52 min in serum was observed after intravenous injection of the drug into a human volunteer.
我们描述了一种使用高效液相色谱法测定血清中头孢呋辛浓度的方法。该药物用二甲基甲酰胺从血清中提取出来,并通过反相色谱法与提取物中的其他物质分离。监测流出物的紫外(280nm)吸收,并根据头孢呋辛峰的高度进行定量。批内和批间不精密度(cv)分别小于3.1%和4.3%。低至1.0mg/升的血清浓度能够被准确测定。未发现来自各种其他药物和抗生素的干扰。在向一名人类志愿者静脉注射该药物后,观察到其在血清中的生物半衰期为52分钟。