Micelle-enhanced spectrofluorimetric method for the rapid determination of bronchodilator terbutaline and its prodrug bambuterol: application for content uniformity test

被引:6
作者
Nour-Eldeen, Deena A. [1 ]
Omar, Mahmoud A. [2 ,3 ]
Mohamed, Salwa Kh [1 ]
Mohamed, Abobakr A. [4 ]
机构
[1] Minia Univ, Fac Pharm, Analyt Chem Dept, Al Minya, Egypt
[2] Taibah Univ, Coll Pharm, Dept Pharmacognosy & Pharmaceut Chem, Al Madinah Almunawarah, Saudi Arabia
[3] Minia Univ, Fac Pharm, Phamaceut Anal Dept, Al Minya, Egypt
[4] Fayoum Univ, Fac Pharm, Pharmaceut Analyt Chem Dept, Al Fayyum, Egypt
关键词
bambuterol hydrochloride; content uniformity test; micellar enhanced; sodium dodecyl sulphate; spectrofluorimetry; terbutaline sulphate; HUMAN PLASMA; PHARMACEUTICALS; DRUG;
D O I
10.1002/bio.4257
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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, similar to 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 mu g ml(-1), with detection limits (LOD) of 0.252 and 0.26 (mu g ml(-1)), quantitation limits (LOQ) of 0.76 and 0.79 (mu g ml(-1)), 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.
引用
收藏
页码:1057 / 1063
页数:7
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