Sentence examples for isocratic reversed-phase from inspiring English sources
Isocratic reversed-phase liquid chromatography with diode array detection was utilized.
A simple, rapid, isocratic reversed-phase high-performance liquid chromatographic method was developed and validated for the analysis of moxonidine and its impurities in tablet formulations.
Isocratic reversed-phase chromatography was performed using acetonitrile/water (40 60), a flow of 1.0 mL min−1, detection at 214 nm, and C18 column (250×4.6 mm2, 5 µm).
In the present study an isocratic reversed-phase high-performance liquid chromatography was investigated for the separation of nimodipine and impurities (A, B and C) using statistical experimental design.
Isocratic reversed-phase HPLC was performed using a Knauer HPLC system (Knauer, Berlin, Germany) with a 5 μ Bondapak C18 column (Waters, Milford, MA, USA).
After enzymatic hydrolysis of serum albumin, aflatoxin B1 lysine adducts were extracted using solid-phase cartridges and separated using isocratic reversed-phase chromatography.
Developed and optimized a validated isocratic reverse phase HPLC separation of Rosuvastatin, Telmisartan, Ezetimibe and Atorvastatin in pharmaceutical preparation using response surface methodology.
Therefore, attempts were made to develop and validate simple, precise, and sensitive, isocratic reverse phase stability indicating high performance liquid chromatographic method for simultaneous determination of both drugs and their degradation products in pharmaceutical formulations.
The diazinon concentration was measured using isocratic reverse-phase HPLC (model of KNAUER, Germany) and the EZ-chrome software with a UV Vis absorbance detector at the wavelength of 269 nm in column C-18.
A rapid, isocratic reverse-phase ultra-performance liquid chromatographic (RP-UPLC) method was developed for the quantitative analysis of the drug, losartan potassium or LOS, in pharmaceutical dosage formulations.
A simple, rapid, sensitive, and validated isocratic reverse-phase ultra-performance liquid chromatographic (RP-UPLC) method was developed and validated for the determination of losartan potassium (LOS) in bulk drug and tablets.
