el Khateeb S Z, Razek S A, Amer M M
Analytical Chemistry Department, Faculty of Pharmacy, Cairo University, Egypt.
J Pharm Biomed Anal. 1998 Aug;17(4-5):829-40. doi: 10.1016/s0731-7085(97)00271-9.
Two spectrophotometric procedures for the selective determination of norfloxacin (NF) in the presence of its decarboxylated degradant are described. The first depends upon measurement of the pH-induced absorbance difference (delta A) of the drug solution between 0.1 N HCl and 0.1 N NaOH at 280 nm. The second involves chelation of the intact drug with iron (II) in acetate buffer solution (pH 5.7 +/- 0.1) to form a yellow-coloured chelate which absorbs at 358 nm. The two procedures are applied successfully for the determination of the intact drug both in pure form and in tablet form. The two methods retain their accuracy in the presence of up to 62% and 76% degradants, respectively.
本文描述了两种分光光度法,用于在诺氟沙星(NF)的脱羧降解产物存在下选择性测定诺氟沙星。第一种方法基于测量药物溶液在280nm处0.1N盐酸和0.1N氢氧化钠之间pH诱导的吸光度差异(ΔA)。第二种方法涉及在醋酸盐缓冲溶液(pH 5.7±0.1)中,完整药物与铁(II)螯合形成黄色螯合物,该螯合物在358nm处有吸收。这两种方法已成功应用于纯品和片剂形式的完整药物的测定。在分别存在高达62%和76%降解产物的情况下,这两种方法仍保持其准确性。