Liu L L, Cheng M, Gao S
Department of Drug Analysis, School of Pharmacy, Changhai Hospital, Second Military Medical University.
Yao Xue Xue Bao. 1994;29(7):539-43.
A column switching HPLC method was established for the determination of norfloxacin, and active dissociation product of silver norfloxacin, in guinea pig plasma and tissues. The pre-treating column (50 mm x 5 mm ID) and analytical column (150 mm x 5 mm ID) were packed with mu-Bondapak C18, 37-50 microns and YWG-C18, 10 microns, respectively. A mixture of CH3OH-0.008 mol/L phosphate buffer-0.05 mol/L tetrabutylammoniun bromide (25:75:4) was used as the analytical mobile phase with a flow rate of 1 ml/min. The pre-treating mobile phase was 0.008 mol/L phosphate buffer with a flow rate of 3 ml/min. UV detection was made at 280 nm. The results were linear within a range of 2-128 micrograms/ml norfloxacin for plasma. The lowest detection limit was 0.25 microgram/ml for plasma. The mean recovery of the method was 102% with a relative standard deviation of less than 7%.
建立了一种柱切换高效液相色谱法,用于测定豚鼠血浆和组织中的诺氟沙星及其活性解离产物诺氟沙星银。预处理柱(内径50 mm×5 mm)和分析柱(内径150 mm×5 mm)分别填充粒径为37 - 50微米的μ - Bondapak C18和粒径为10微米的YWG - C18。以甲醇 - 0.008 mol/L磷酸盐缓冲液 - 0.05 mol/L四丁基溴化铵(25:75:4)的混合物作为分析流动相,流速为1 ml/min。预处理流动相为0.008 mol/L磷酸盐缓冲液,流速为3 ml/min。于280 nm波长处进行紫外检测。血浆中诺氟沙星浓度在2 - 128微克/毫升范围内结果呈线性。血浆最低检测限为0.25微克/毫升。该方法的平均回收率为102%,相对标准偏差小于7%。