Enantioselective method development and validation of proline by using high performance liquid chromatography

Authors

  • Nagamalleswari Gampa Department of Pharmaceutical Analysis, Chalapathi Institute of Pharmaceutical Sciences, Lam, Guntur, Andhra Pradesh
  • Prachet Pinnamaneni Department of Pharmaceutical Analysis, Chalapathi Institute of Pharmaceutical Sciences, Lam, Guntur, Andhra Pradesh
  • Naga Thirumalesh Chevala Department of Pharmaceutical Analysis, Chalapathi Institute of Pharmaceutical Sciences, Lam, Guntur, Andhra Pradesh
  • Geervani Pamidimarri Department of Pharmaceutical Analysis, Chalapathi Institute of Pharmaceutical Sciences, Lam, Guntur, Andhra Pradesh
  • Arulsamy Elphine Prabahar Department of Pharmaceutical Analysis, Chalapathi Institute of Pharmaceutical Sciences, Lam, Guntur, Andhra Pradesh
  • Venkata Suresh Ponnuru Department of Pharmaceutical Analysis, Chalapathi Institute of Pharmaceutical Sciences, Lam, Guntur, Andhra Pradesh
  • Rama Rao Nadendla Department of Pharmaceutical Analysis, Chalapathi Institute of Pharmaceutical Sciences, Lam, Guntur, Andhra Pradesh

DOI:

https://doi.org/10.7439/ijapa.v6i1.3454

Abstract

Chirality is a major concern in the modern pharmaceutical industry. The separation of chiral compounds has been of great interest because the majority of bioorganic and synthetic molecules are chiral. Aim of the present investigation was to develop a stereo specific, simple and precise normal phase high performance liquid chromatography (NP - HPLC) method for the separation and enantiopurity of Dextro (D) and Levo (L) enantiomers of proline (PRO) by using Lux 5m Amylose 1 LC column (250.6mm) by using n- Hexane: Iso propyl alcohol (IPA)as mobile phase in the ratios of 90:10 v/v at flow rate of 1.2 ml/ min. D and L forms of PRO was detected at 210nm with retention time of 8.1min and 9 min respectively with correlation coefficient (R 2 ) of 0.999.The method was validated with reference to International conference of harmonization (ICH) in terms of linearity, accuracy, precision (Inter - day and intra - day precision), limit of detection (LOD), limit of quantification (LOQ), stability of test solutions, specificity, system suitability, robustness and ruggedness.

Downloads

Download data is not yet available.

Downloads

Published

2016-03-30

Issue

Section

Research Articles

How to Cite

1.
Enantioselective method development and validation of proline by using high performance liquid chromatography. Int J of Adv in Phar Ana [Internet]. 2016 Mar. 30 [cited 2025 Mar. 15];6(1):05-8. Available from: https://ssjournals.co.in/index.php/ijapa/article/view/3454