Department of Analytical Chemistry and Foods Technology, University of Castilla-La Mancha, 13071 Ciudad Real, Spain.
Appl Spectrosc. 2013 Apr;67(4):371-8. doi: 10.1366/12-06776.
A simple luminescent methodology for the simultaneous determination of doxycycline and chlortetracycline in pharmaceutical preparations and human urine is proposed. Since the native fluorescence of both analytes is negligible, this method takes advantage of the lanthanide-sensitized luminescence, which provides increased sensitivity. Due to the strong overlapping between the luminescence spectra of both europium complexes, the use of luminescence decay curves to resolve mixtures of the analytes is proposed, particularly as these curves are more selective. A factorial design, with three levels per factor, coupled to a central composite design was selected to obtain a calibration matrix of 13 standards plus one blank sample, which were processed with a partial least-squares analysis. In order to assess the effectiveness of the proposed method, a prediction set of 10 synthetic samples was analyzed, and recovery percentages between 95 and 104% were obtained. Limits of detection, calculated by means of a new criterion, were 3.27 and 1.06 μg L(-1) for doxycycline and chlortetracycline, respectively. The method was tested in three different pharmaceutical preparations containing the analytes, with average recovery percentages of 99.4 ± 1.8 for doxycycline and 100.5 ± 2.1 for chlortetracycline. Moreover, a central composite design was also developed to obtain a calibration matrix that made feasible the simultaneous determination of both tetracyclines in human urine samples. In this case, average recovery percentages were 98.0 ± 4.4 and 97.8 ± 4.6 for doxycycline and chlortetracycline, respectively. No extraction method or prior separation of the analytes was needed.
提出了一种简单的荧光法,用于同时测定药物制剂和人尿中的强力霉素和金霉素。由于两种分析物的固有荧光可以忽略不计,因此该方法利用了镧系元素敏化的荧光,从而提高了灵敏度。由于两种铕配合物的荧光光谱有很强的重叠,因此建议使用荧光衰减曲线来解析分析物的混合物,尤其是因为这些曲线更具选择性。选择了具有三个水平的因子设计,并结合中心复合设计,以获得包括一个空白样品在内的 13 个标准品的校准矩阵,并用偏最小二乘分析对其进行处理。为了评估所提出方法的有效性,分析了一组 10 个合成样品的预测集,并获得了 95%至 104%的回收率。通过一种新的标准计算得到的检测限分别为强力霉素和金霉素的 3.27 和 1.06μg/L。该方法在三种含有分析物的不同药物制剂中进行了测试,强力霉素的平均回收率为 99.4±1.8%,金霉素的平均回收率为 100.5±2.1%。此外,还开发了中心复合设计,以获得校准矩阵,从而能够同时测定人尿样中的两种四环素。在这种情况下,强力霉素和金霉素的平均回收率分别为 98.0±4.4%和 97.8±4.6%。不需要提取方法或对分析物进行预先分离。