"Simultaneous quantification of nystatin, triamcinolone acetonide, neomycin sulfate and gramicidin D in transferosomal gel by rapid stability indicating HPLC method with PDA detector".

Rapid quantitative determination of zidovudine, lamivudine and nevirapine drugs in pharmaceutical tablets by stability-indicating monolithic liquid chromatography: validation, greenness, blueness and whiteness studies.

A simple, rapid, stability-indicating high-performance liquid chromatography method was developed and validated for simultaneous determination of lamivudine, zidovudine and nevirapine in pharmaceutical formulations and was successfully applied for the simultaneous quantitative analysis of 3TC, ZDV and NVP in tablet dos...

Simultaneous Determination of Doxecitine and Doxribtimine in Bulk Drug and Pharmaceutical Formulation by Reverse-phase Ultra-performance Liquid Chromatographic with Photodiode Array Detection: Method Development and Validation

SIMULTANEOUS QUANTIFICATION OF PARACETAMOL, GUAIFENESIN AND PHENYLEPHRINE HYDROCHLORIDE BY STABILITY-INDICATING RP-HPLC IN PHARMACEUTICAL TABLETS

A simple, accurate, and precise reverse-phase high-performance liquid chromatography method was for developed simultaneously estimating paracetamol, guaifenesin, and phenylephrine hydrochloride in a combined dosage form. An Inertsil ODS-3V C18 column (250 mm × 4.6 mm, 5 µm) was used to separate the samples. The mobile...

Glycopyrronium bromide, formoterol fumarate dihydrate and their related compounds with UPLC/PDA-MS for simultaneous determination in pressurized metered-dose inhaler product

abstract An ultra-performance liquid chromatography (UPLC) technique with photodiode array-mass spectrometry (PDA-MS) detectors has been developed and validated for the determination of glycopyrronium bromide (GB), formoterol fumarate dihydrate (FFD) and their related substances in pressurized meter dose inhalers. This...

RP-HPLC Method Development and Validation for Simultaneous Estimation of Paracetamol and Prochlorperazine Maleate

The proposed RPHPLC method was found to be reliable, sensitive, accurate, and suitable for routine quality control analysis and stability assessment of Paracetamol and Prochlorperazine Maleate in pharmaceutical formulations.

A NOVEL GREEN ASSESSMENT ANALYTICALMETHODTOQUANTIFY THE CONTENT OF DIMETHYLGLYOXIMEINLENALIDOMIDE USING LC-MS

These proposed separation strategies showed high specificity, substantiating clear resolution of DMG foreign substance by the drug compound, also with foreign substances, and confirmed the method’s suitability for both regulatory compliance and routine application in industrial Quality Control laboratories.