Analytical Chemistry Department, Faculty of Pharmacy, Minia University, Minia, Egypt.
Department of Pharmacognosy and Pharmaceutical Chemistry, College of Pharmacy, Taibah University, Al Madinah AlMunawarah, Saudi Arabia.
Luminescence. 2022 Jul;37(7):1057-1063. doi: 10.1002/bio.4257. Epub 2022 Jun 3.
A novel, simple and sensitive spectrofluorimetric approach for determination of terbutaline sulphate (TER) and its prodrug bambuterol (BAM) in their pure and pharmaceutical dosage forms was developed. The suggested approach depends on enhancing the native fluorescence of either TER or BAM at 315 and 297.2 nm after excitation at 277 and 259 nm, respectively, using sodium dodecyl sulphate (SDS) as a micellar medium. In the presence of 0.7% w/v SDS, ~1.38-fold and 1.18-fold enhancement is achieved in the relative fluorescence intensity (RFI) of TER and BAM, respectively. The fluorescence-concentration curves were rectilinear over the concentration range 0.8-16 μg ml , with detection limits (LOD) of 0.252 and 0.26 (μg ml ), quantitation limits (LOQ) of 0.76 and 0.79 (μg ml ), determination coefficients (r2) of 0.9981, and slopes of 45.92 and 10.44 for TER and BAM, respectively. The suggested approach was validated in accordance with International Council for Harmonisation criteria and was effectively applied in the analysis of the studied drugs in their commercial tablets. The high sensitivity of the proposed approach allows its application in evaluating the content uniformity testing of the studied drugs in their tablets through using the official United States Pharmacopeia criteria. Statistical analogies of the findings with that of the reported methods showed really good harmony and indicated no major differences in precision and accuracy.
开发了一种新颖、简单和灵敏的分光荧光法,用于测定硫酸特布他林(TER)及其前药班布特罗(BAM)在纯品和药物制剂中的含量。该方法基于在 277nm 和 259nm 分别激发下,利用十二烷基硫酸钠(SDS)作为胶束介质增强 TER 或 BAM 的本征荧光,在 315nm 和 297.2nm 处分别检测。在 0.7%w/v SDS 存在下,TER 和 BAM 的相对荧光强度(RFI)分别提高了约 1.38 倍和 1.18 倍。荧光-浓度曲线在 0.8-16μgml 的浓度范围内呈线性,TER 和 BAM 的检测限(LOD)分别为 0.252 和 0.26(μgml),定量限(LOQ)分别为 0.76 和 0.79(μgml),决定系数(r2)分别为 0.9981,斜率分别为 45.92 和 10.44。该方法符合国际协调理事会的验证标准,并有效地应用于其商业片剂中研究药物的分析。所提出方法的高灵敏度允许其通过使用官方美国药典标准来评估研究药物片剂的含量均匀度测试。与报道方法的结果进行统计学比较表明,它们之间具有良好的一致性,并且在精密度和准确度方面没有显著差异。