Advanced spectrophotometric methods for quantitative assessment of two antihypertensive drugs in mixture with hydrochlorothiazide in pure form and pharmaceutical formulations

被引:1
|
作者
Salem, Maissa Y. [1 ]
Hassan, Nagiba Y. [1 ]
Fayez, Yasmin M. [1 ]
Sabour, Samah A. [2 ]
Ali, Enas S. [2 ]
机构
[1] Cairo Univ, Dept Analyt Chem, Fac Pharm, Kasr El Aini, Cairo 11562, Egypt
[2] Natl Org Drug Control & Res NODCAR, Giza, Egypt
关键词
Labetalol; Nebivolol; Constant center; Advanced absorbance subtraction; Absorption factor; Ratio subtraction; PERFORMANCE LIQUID-CHROMATOGRAPHY; BETA-BLOCKERS; SPECTROFLUOROMETRIC DETERMINATION; CARDIOVASCULAR DRUGS; BINARY-MIXTURES; HUMAN URINE; LABETALOL; METABOLITE; TABLETS; SERUM;
D O I
10.1007/s13738-019-01699-y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Labetalol (Lab) and nebivolol (Neb) are beta-adrenoceptor blocking agents that are employed for control of hypertension alone or co-administered with hydrochlorothiazide (HCTZ) as a potent diuretic for synergistic antihypertensive effect. Advanced, accurate and simple spectrophotometric methods with minor manipulation of zero-order spectra were suggested for simultaneous quantitation of Lab or Neb in mixture with HCTZ for quality control purpose in pure form and pharmaceutical formulations. These methods include (a) constant center method, (b) advanced absorbance subtraction method for Lab and HCTZ, (c) absorption factor method (AFM) and (d) the ratio subtraction method. The established methods were successfully applied over concentration ranges 10-100 mu g/mL, 10-75 mu g/mL and 2.5-25 mu g/mL of Lab, Neb and HCTZ, respectively. Results were compared statistically to those of official and reported methods revealing no remarkable difference. Validation of methods followed international conference of harmonization guidelines. Suggested methods require minor processing of zero-order spectra with accurate results that facilitate the quantitative estimation of studied mixtures in quality control laboratories.
引用
收藏
页码:2257 / 2268
页数:12
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