Analytical method of development and validation of rivaroxaban in bulk drug and pharmaceutical drugs from RP-HPLC
I have done research and achieved the method of development and validation of Rivaroxaban in bulk drug and pharmaceutical dosage form by RP-HPLC method. The analysis of drug carried out an agilent technique gradient system with auto injector, UV(DAD) and Gradient detector. Equipped with reverse phase (agilent) C18 column (4.6mm * 100mm; 2.5 um), 20 ul injection loop and UVD30D absorbance detector and running chemstration 10.1 software. Methanol and 0.1% formic acid (65:35).
Authors
- Poonam P Warade
- Dipak D Kumbhar
- Rupali Patil (ORCID: https://orcid.org/0000-0002-7291-2370)
- Rajesh G Jadhao
- Suvarna Saraf
Institutions
- Pew Charitable Trusts (US)
Publication Details
- Journal
- GSC Biological and Pharmaceutical Sciences
- Published
- 2025-08-26
- DOI
- https://doi.org/10.30574/gscbps.2025.32.2.0317
- Primary Topic
- Analytical Methods in Pharmaceuticals
- Type
- article
- Field-Weighted Citation Impact
- 0.00