GET THE APP

Method Development and Validation of Milnacipran by using RP-HPLC Method | Abstract

Asian Journal of Pharmaceutical Technology and Innovation (ajpti)

All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.

Method Development and Validation of Milnacipran by using RP-HPLC Method

Abstract

Palleppagari Sridhar*, K. Venkateswar Rao, C. Radhika, A. Sujitha, V. Uma Maheswara Rao

A rapid and precise reverse phase high performance liquid chromatographic method has been developed for the validated of Milnacipran, in its pure form as well as in capsule dosage form. Chromatography was carried out on a phenomanix C18 (4.6 x 250mm, 5µm) column using a mixture of Acetonitrile: Triethylamine buffer pH 4.5(65:35% v/v)as the mobile phase at a flow rate of 0.8ml/min, the detection was carried out at 215 nm. The retention time of the Milnacipran was 2.16 min respectively. The method produce linear responses in the concentration range 5-25 mg/ml of Milnacipran. The method precision for the determination of assay was below 2.0% RSD. The method is useful in the analysis of bulk and pharmaceutical formulations of Millancipran.

Share this article

tempobet

tempobet giriş

tempobet giriş

paper.io

agar io

wowcappadocia.com cappadocia tours
cappadocia-hotels.com cappadocia hotels
caruscappadocia.com cappadocia hotel
brothersballoon.com cappadocia balloon
balloon-rides.net cappadocia balloon flights

wormax io