Raghu Madihalli Srinivas, Basavaiah Kanakapura, Prashanth Kudige Nagaraj, Vinay Kanakapura Basavaiah
Department of Chemistry, University of Mysore, Manasagangotri, Mysore, Karnataka 570006, India.
Int J Anal Chem. 2013;2013:697651. doi: 10.1155/2013/697651. Epub 2013 Nov 12.
One titrimetric and two spectrophotometric methods are described for the determination of ketotifen fumarate (KTF) in bulk drug and in tablets using cerium(IV) as the oxidimetric agent. In titrimetry (method A), the drug was treated with a measured excess of cerium(IV) in H2SO4 medium and after a standing time of 10 min, the surplus oxidant was determined by back titration with iron(II). The spectrophotometric procedures involve addition of a known excess of cerium(IV) to KTF in acid medium followed by the determination of unreacted oxidant by reacting with either p-dimethyl amino benzaldehyde and measuring the resulting colour at 460 nm (method B) or o-dianisidine and subsequent measurement of the absorbance of coloured product at 470 nm (method C). Titrimetric assay is based on a 1 : 2 reaction stoichiometry between KTF and cerium(IV) and the method is applicable over 2-18 mg range. In spectrophotometry, regression analysis of Beer's law plots showed a good correlation in 0.4-8.0 and 0.4-10.0 g mL(-1) KTF ranges for method B and method C, respectively, and the corresponding molar absorptivity coefficients are calculated to be 4.0 × 10(4) and 3.7 × 10(4) L mol(-1) cm(-1).
描述了一种滴定法和两种分光光度法,用于测定原料药和片剂中的富马酸酮替芬(KTF),以铈(IV)作为氧化测定剂。在滴定法(方法A)中,将药物在硫酸介质中用过量的铈(IV)处理,静置10分钟后,用亚铁进行回滴定来测定剩余的氧化剂。分光光度法包括在酸性介质中向KTF中加入已知过量的铈(IV),然后通过与对二甲氨基苯甲醛反应并在460nm处测量产生的颜色(方法B)或与邻联茴香胺反应并随后在470nm处测量有色产物的吸光度(方法C)来测定未反应的氧化剂。滴定法测定基于KTF与铈(IV)之间1∶2的反应化学计量比,该方法适用于2 - 18mg范围。在分光光度法中,比尔定律曲线的回归分析表明,方法B和方法C在KTF浓度分别为0.4 - 8.0和0.4 - 10.0μg mL⁻¹范围内具有良好的相关性,相应的摩尔吸光系数经计算分别为4.0×10⁴和3.7×10⁴L mol⁻¹cm⁻¹。