Pragourpun Kraivinee, Sakee Uthai, Fernandez Carlos, Kruanetr Senee
Center of Excellence for Innovation in Chemistry and Department of Chemistry (PERCH-CIC), Faculty of Science, Mahasarakham University, Kantarawichai District, Mahasarakham 44150, Thailand.
School of Pharmacy and Life Sciences, Robert Gordon University, Aberdeen AB10 7GJ, United Kingdom.
Spectrochim Acta A Mol Biomol Spectrosc. 2015 May 5;142:110-7. doi: 10.1016/j.saa.2015.01.081. Epub 2015 Feb 9.
We present for the first time the use of deferiprone as a non-toxic complexing agent for the determination of iron by sequential injection analysis in pharmaceuticals and food samples. The method was based on the reaction of Fe(III) and deferiprone in phosphate buffer at pH 7.5 to give a Fe(III)-deferiprone complex, which showed a maximum absorption at 460nm. Under the optimum conditions, the linearity range for iron determination was found over the range of 0.05-3.0μgmL(-1) with a correlation coefficient (r(2)) of 0.9993. The limit of detection and limit of quantitation were 0.032μgmL(-1) and 0.055μgmL(-1), respectively. The relative standard deviation (%RSD) of the method was less than 5.0% (n=11), and the percentage recovery was found in the range of 96.0-104.0%. The proposed method was satisfactorily applied for the determination of Fe(III) in pharmaceuticals, water and food samples with a sampling rate of 60h(-1).
我们首次展示了去铁酮作为一种无毒络合剂,用于通过顺序注射分析法测定药品和食品样品中的铁。该方法基于Fe(III)与去铁酮在pH 7.5的磷酸盐缓冲液中反应生成Fe(III)-去铁酮络合物,该络合物在460nm处有最大吸收。在最佳条件下,铁测定的线性范围为0.05 - 3.0μgmL(-1),相关系数(r(2))为0.9993。检测限和定量限分别为0.032μgmL(-1)和0.055μgmL(-1)。该方法的相对标准偏差(%RSD)小于5.0%(n = 11)且回收率在96.0 - 104.0%范围内。所提出的方法以60h(-1)的采样率成功应用于药品、水和食品样品中Fe(III)的测定。