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

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

A Stability-Indicating RP-HPLC Approach for the Simultaneous Determination of Linagliptin and Dapagliflozin in Bulk and Marketed Formulation

A simple, rapid, accurate, precise, and stability-indicating reversed-phase high-performance liquid chromatographic (RP-HPLC) method was developed and validated for the simultaneous determination of linagliptin (LNG) and dapagliflozin (DPM) in bulk drug and tablet dosage forms. Chromatographic separation was accomplish...

To develop and validate the stability indicating method for Empagliflozin and Linagliptin using HPLC method

The developed RP HPLC method is simple, rapid, selective, accurate, economical, and can be used for routine pharmaceutical quality control, stability testing and analysis of combined Linagliptin and Empagliflozin formulation.

Method Development, Validation and Estimation of Single Synthetic Drug Tafamidis by RP-HPLC and Green Analysis in API Form and Pharmaceutical Dosage Form

For the quantitative determination of Tafamidis in bulk and pharmaceutical dosage forms, a straightforward, accurate, precise, and environmentally friendly reverse-phase high-performance liquid chromatographic (RP-HPLC) method was developed and validated. To achieve optimal chromatographic performance, several stationa...

A Validated Reversed Phase‐High Performance Liquid Chromatographic Method for Simultaneous Estimation of Bisoprolol Fumarate, Cilnidipine, and Telmisartan With RGB12‐Based Sustainability Assessment

The simultaneous estimation of multiple antihypertensive agents in fixed‐dose combination formulations requires robust and reliable analytical methods. A validated RP‐HPLC method for the simultaneous estimation of bisoprolol fumarate, cilnidipine, and telmisartan with robustness assessment using Box–Behnken Design...

Development, validation, and greenness assessment of UV spectrophotometric and RP-HPLC methods for the quantitative determination of Nafithromycin

Nafithromycin is a novel ketolide antibiotic approved for the treatment of community-acquired bacterial pneumonia (CABP). The present study describes the development and validation of UV spectrophotometric and reverse-phase high-performance liquid chromatographic (RP-HPLC) methods for the quantitative determination of...