Method development and validation for the estimation of Divalproex sodium by using RP-HPLC in bulk and pharmaceutical dosage forms

Journal Title: Indian Journal of Research in Pharmacy and Biotechnology - Year 2018, Vol 6, Issue 2

Abstract

New RP HPLC method was developed for the estimation of Divalproex Sodium pharmaceutical dosage form. Solubility of Divalproex sodium was determined using various solvents and buffers. Absorption maxima of the drug in UV–Visible region in different solvents/buffers was determined and different solvents were tried for HPLC method development. Mobile phase was optimized and flow rates for proper resolution and retention times. HPLC method was validated as per ICH guidelines.

Authors and Affiliations

M. Fatima Rose, Chattumala Anand Kumar, Injamuri Diwakar, Jangam Vanaja, Kottu Gayathri, Julakanti Likhitha, Hassan EaisaMohamed Hamid

Keywords

Related Articles

Potential Impact of Nanomaterials in Information and Communication Technologies

Nanomaterials are throwing the doors open to a hyper-tech era in which electronics and information and communication technology (ICT) are going to become ubiquitous. Enormous progress has been made by making a transiti...

Study on Soaking and Germination Times on Moisture and Volume amounts of Malt produced from two varieties of Barely Using response Surface Methodology

Hordeumvulgaredried and germinated under controlled conditions. In this study two barely lines EBYT-88- 20, EBYT-88-17 used and their malt production ability measured. Combination of germination and soaking times inclu...

An Assessment on RO water plants in Karimnagar District

Purity of drinking water plays vital role on people’s health. At present people are drinking the RO water from mineral plants. We have collected the samples various parts of the Karimnagar district. Majority of the min...

RECENT TRENDS OF POLYMER USAGE IN THE FORMULATION OF ORODISPERSIBLE TABLETS

Disintegrants are an essential component to tablet formulations. While rapidly disintegrating tablets do not necessarily ensure fast bioavailability, slowly disintegrating tablets almost always assure slow bioavailabil...

EFFECT OF HYDROTROPIC SOLUTE ON In-VitroCHARECTERIZATION OF VALSARTAN FAST DISINTEGRATING TABLETS

Valsartan is an angiotensin receptor antagonist, commonly called as “angiotensin receptor blocker", or angiotensin receptor blocker. Solubility is an important physicochemical factor affecting absorption of drug and it...

Download PDF file
  • EP ID EP33511
  • DOI -
  • Views 329
  • Downloads 0

How To Cite

M. Fatima Rose, Chattumala Anand Kumar, Injamuri Diwakar, Jangam Vanaja, Kottu Gayathri, Julakanti Likhitha, Hassan EaisaMohamed Hamid (2018). Method development and validation for the estimation of Divalproex sodium by using RP-HPLC in bulk and pharmaceutical dosage forms. Indian Journal of Research in Pharmacy and Biotechnology, 6(2), -. https://europub.co.uk/articles/-A-33511