Institute of Chemical Sciences, University of Peshawar, Pakistan.
Luminescence. 2013 Sep-Oct;28(5):719-25. doi: 10.1002/bio.2422. Epub 2012 Sep 17.
A sensitive and accurate spectrofluorimetric method has been developed for the determination of sulpiride in pharmaceutical preparations and human plasma. The developed method is based on the derivatization reaction of 2-cyanoacetamide with sulpiride in 30% ammonical solution. The fluorescent derivatized reaction product exhibited maximum fluorescence intensity at 379 nm after excitation at 330 nm. The optimum conditions for derivatization reactions were studied and the fluorescence intensity versus concentration plot was found to be linear over the concentration range 0.2-20.0 µg/mL with a correlation coefficient of 0.9985. The limit of detection (LOD) and limit of quantification (LOQ) were found to be 0.82 and 2.73 ng/mL, respectively. The proposed method was validated according to ICH guidelines. The effects of common excipients and co-administered drugs were also studied. The accuracy of the method was checked using the standard addition method and percent recoveries were found to be in the range of 99.00-101.25% for pharmaceutical preparations and 97.00-97.80% for spiked human plasma. The method was successfully applied to commercial formulations and the results obtained for the proposed method were compared with a high-performance liquid chromatography reference method and statistically evaluated using the Student's t-test for accuracy and the variance ratio F-test for precision. A reaction pathway was also proposed.
一种灵敏、准确的荧光分光光度法已被开发用于测定药物制剂和人血浆中的舒必利。该方法基于在 30%氨水溶液中,2-氰基乙酰胺与舒必利的衍生化反应。衍生化反应产物在 330nm 激发下于 379nm 处显示出最大荧光强度。对衍生化反应的最佳条件进行了研究,发现荧光强度与浓度的关系在 0.2-20.0μg/mL 浓度范围内呈线性关系,相关系数为 0.9985。检测限(LOD)和定量限(LOQ)分别为 0.82 和 2.73ng/mL。该方法按照 ICH 指南进行了验证。还研究了常见赋形剂和共同给药药物的影响。使用标准加入法检查了该方法的准确性,发现对于药物制剂,回收率在 99.00-101.25%之间,对于加标人血浆,回收率在 97.00-97.80%之间。该方法已成功应用于商业制剂,所得结果与高效液相色谱参考方法进行了比较,并使用学生 t 检验对准确性和方差比 F 检验对精密度进行了统计学评估。还提出了一个反应途径。