Ahmad Iqbal, Anwar Zubair, Sheraz Muhammad Ali, Ahmed Sofia, Khattak Saif-Ur-Rehman
Baqai Institute of Pharmaceutical Sciences, Baqai Medical University, Karachi, Pakistan.
Central Drug Laboratories, Ministry of Health, DRAP, Block-B, S.M.C.H., Karachi, Pakistan.
Luminescence. 2018 Sep;33(6):1070-1080. doi: 10.1002/bio.3510. Epub 2018 Jul 8.
A stability-indicating spectrofluorimetric method has been developed for the simultaneous assay of riboflavin (RF) and photoproducts, formylmethylflavin (FMF), lumichrome (LC) and lumiflavin (LF) in aqueous solution. The method is based on the extraction of LC formed in acid solution and LC and LF formed in alkaline solution with chloroform at pH 2.0 and their assay by fluorescence measurements at 478 and 530 nm, respectively. The aqueous phase, on readjustment of the pH to 6.5, is used to extract FMF with chloroform and its assay is carried out at 530 nm. The aqueous phase is then used for the assay of RF at 530 nm. The proposed method gives more accurate results for the assay of RF compared to those of the United States Pharmacopeia (USP) spectrofluorimetric method which does not take into account the presence of RF photoproducts having similar fluorescence characteristics. The proposed method along with the USP method has been applied to the study of the kinetics of photolysis of RF, assay of stored commercial vitamin preparations and their radiated samples. The results show that the USP method does not distinguish between the fluorescence of RF and its photoproducts, and, therefore, gives erroneous results with about 11% excess in the quantity of the vitamin compared to that of the proposed method. This is due to the interference of the fluorescence of photoproducts in the assay of RF. The method has been validated for various analytical parameters according to the guideline of the International Council for Harmonization (ICH).
已开发出一种稳定性指示荧光分光光度法,用于同时测定水溶液中的核黄素(RF)及其光产物、甲酰甲基黄素(FMF)、光色素(LC)和光黄素(LF)。该方法基于在pH 2.0条件下,用氯仿萃取酸性溶液中形成的LC以及碱性溶液中形成的LC和LF,并分别通过在478和530 nm处的荧光测量进行测定。将水相的pH值重新调至6.5后,用于用氯仿萃取FMF,并在530 nm处进行测定。然后将水相用于在530 nm处测定RF。与美国药典(USP)荧光分光光度法相比,所提出的方法在测定RF时能给出更准确的结果,USP方法未考虑具有相似荧光特性的RF光产物的存在。所提出的方法与USP方法已应用于RF光解动力学研究、市售维生素制剂及其辐射样品的测定。结果表明,USP方法无法区分RF及其光产物的荧光,因此,与所提出的方法相比,维生素含量会给出错误结果,约有11%的过量。这是由于光产物荧光在RF测定中产生干扰。该方法已根据国际协调理事会(ICH)的指南对各种分析参数进行了验证。