Method Development and Validation of Latanoprost by using RP-HPLC in Pharmaceutical Formulations

Authors

  • K.Srinivas
  • D.Narendra
  • P.V.V.Varaprasad
  • G.Jaya durga madhuri
  • K.Eswari
  • N.Shanti priya VJ’s College of Pharmacy, Diwancheruvu, Rajamahendravaram, Andhra Pradesh, India.

DOI:

https://doi.org/10.47070/ijraps.v7i4.142

Keywords:

Latanoprost, RP-HPLC, Precision, Validation.

Abstract

Chromatography was performed with a mobile phase containing a methanol of assay (99.8%) with flow rate of 1ml/min. Quantitation was accomplished with an internal standard method. The procedure was validated for linearity (correlation coefficient = 0.990), accuracy and Limit of detection (LOD) intraday precision. To test validation of the Latanoprost three factors were considered as linearity, precision, LOD where mobile phase, flowrate and pressure are respectively selected as methanol, 1 ml/min, 1600 pascals.

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Published

22-04-2023

How to Cite

1.
K.Srinivas, D.Narendra, P.V.V.Varaprasad, G.Jaya durga madhuri, K.Eswari, N.Shanti priya. Method Development and Validation of Latanoprost by using RP-HPLC in Pharmaceutical Formulations. IJRAPS [Internet]. 2023 Apr. 22 [cited 2025 Jul. 6];7(4):14-6. Available from: https://ijraps.in/index.php/ijraps/article/view/142

Issue

Vol 7, Issue 4: April 2023

Section

Articles