Abstract

A REVIEW ON RP- HPLC ANAYTICAL METHODS FOR ESTIMATION OF SELEXIPAG IN PHARMACEUTICAL DOSAGE FORM

Vaishnavi P. Wagh*, Dr. Gokul S. Talale and Seema Ugale

ABSTRACT

A method for determining the amount of Selexipag in pharmaceutical tablet dosage form has been developed and verified. It is straightforward, efficient, precise, accurate, and stable. For Selexipag, an effective high performance liquid chromatographic technique was created. It was discovered that the HPLC procedure was precise, accurate, affordable, and repeatable. Chromatography is largely used in chemical analysis, where it serves as a separation technique. One particularly versatile method is high-performance liquid chromatography (HPLC), which separates analyses by passing them through a column filled with particles that are micrometer in size. The technique can be recommended for both routine analysis and the identification of the relative and substance- related components of Selexipag in pharmaceutical dose form. A significant part in
pulmonary arterial hypertension is played by Selexipag these medications are now readily accessible on the market in both single and mixed dosage forms. Selexipag is an oral medication that functions as a long-acting agonist for IP receptors.

Keywords: Receptor agonist, hypertension, chromatography, HPLC, analytical technique, and Selexipag.