Yoshida Y, Sato E, Moroi R
Drug Metabolism & Analytical Chemistry Research Center, Daiichi Pharmaceutical Co., Ltd., Tokyo, Japan.
Arzneimittelforschung. 1993 May;43(5):601-6.
The photodegradation of levofloxacin (DR-3355, CAS 100986-85-4), the S-(-)-isomer of ofloxacin, was investigated. Levofloxacin in aqueous solution was exposed to near ultraviolet light (peak wavelength 352 nm) for 16 h at room temperature. Nine degradation products (P-2-P-10) were isolated from the reaction mixture by preparative high performance liquid chromatography. The structures of these compounds were deduced from their NMR, MS, UV and IR spectra and optical rotations. The elucidated structures showed that all of these degradation products were analogues altered at the N-methylpiperazine moiety of levofloxacin.
对氧氟沙星的 S-(-)-异构体左氧氟沙星(DR-3355,CAS 100986-85-4)的光降解进行了研究。将水溶液中的左氧氟沙星在室温下暴露于近紫外光(峰值波长 352 nm)下 16 小时。通过制备型高效液相色谱从反应混合物中分离出九种降解产物(P-2 - P-10)。根据这些化合物的核磁共振谱、质谱、紫外光谱、红外光谱和旋光度推断其结构。所阐明的结构表明,所有这些降解产物都是左氧氟沙星 N-甲基哌嗪部分发生改变的类似物。