Ultrasound assisted dispersive liquid-liquid microextraction coupled with high performance liquid chromatography designated for bioavailability studies of felodipine combinations in rat plasma

被引:15
作者
Ahmed, Sameh [1 ,2 ]
Atia, Noha N. [2 ]
Ali, Marwa Fathy Bakr [2 ]
机构
[1] Taibah Univ, Pharmacognosy & Pharmaceut Chem Dept, Coll Pharm, Al Madinah Almunawarah 30001, Saudi Arabia
[2] Assiut Univ, Fac Pharm, Dept Pharmaceut Analyt Chem, Assiut 71526, Egypt
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2017年 / 1046卷
关键词
Felodipine; Ultrasound; Dispersive extraction; Therapeutic drug monitoring; Bioavailability study; TANDEM MASS-SPECTROMETRY; ACTIVE METABOLITE RAMIPRILAT; CALCIUM-CHANNEL ANTAGONISTS; CHIRAL STATIONARY-PHASE; FLUORESCENCE DETECTION; SIMULTANEOUS QUANTITATION; ALPHA-HYDROXYMETOPROLOL; METOPROLOL SUCCINATE; GAS-CHROMATOGRAPHY; MS-MS;
D O I
10.1016/j.jchromb.2017.01.034
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Felodipine (FLD), a calcium channel antagonist, is commonly prescribed for the treatment of hypertension either with Metoprolol (MET) or Ramipril (RAM) in two different drug combinations. FLD has high plasma protein binding ability affecting, its extraction recoveries from plasma samples. Hence, a specific ultrasound assisted dispersive liquid-liquid microextraction (UA-DLLME) method coupled with HPLC using photodiode array detector was developed and validated for the simultaneous determination of FLD, MET and RAM in rat plasma after oral administration of these combinations. The factors affecting UA-DLLME were carefully optimized. In this study, UA-DLLME method could provide simple and efficient plasma extraction procedures with superior recovery results. Under optimum condition, all target drugs were separated within 13 min. The validation procedures was carried out in agreement with US-FDA guidelines and shown to be suitable for anticipated purposes. Linear calibration ranges were obtained in the range 0.05-2.0 mu gmL(-1) for FLD and MET and 0.1-2.0 mu gmL(-1) for RAM with detection limits of 0.013-0.031 mu gmL(-1) for all the studied drug combinations. The%RSD for inter-day and intra-day precisions was in range of 0.63-3.85% and the accuracy results were in the range of 92.13-100.5%. The validated UA-DLLME-HPLC method, was successfully applied for the bioavailability studies of FLD, MET and RAM. The pharmacokinetic parameters were calculated for all the investigated drugs in rats after single-dose administrations of two different drug combinations. Although FLD was bioequivalent in the two formulations, a small increase in plasma levels of MET and RAM was found in the presence of FLD. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:200 / 210
页数:11
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