Research Journal of Pharmacy and Technology

SCOPUS
  • Year: 2021
  • Volume: 14
  • Issue: 11

Method development and validation for pyrogallol content quantification by hplc in trimetazidine dihydrochloride

  • Author:
  • Durgababu Rapeti1, Kapavarapu Maruthi Venkata Narayanarao1, Pulipaka Shyamala2, Rallabhandi Murali Krishna3
  • Total Page Count: 5
  • Page Number: 5803 to 5807

1GVK Biosciences Pvt Ltd, Hyderabad, Telangana, India - 500076

2Physical Chemistry DepartmentAndhra University, Visakhapatnam, Andhra Pradesh, India - 530003

3Department of Physical and Nuclear chemistry, and Department of Chemical Oceanography, Andhra University, Visakhapatnam, Andhra Pradesh, India - 530003

*Corresponding Author E-mail: durgababu_chem416@yahoo.com

Online Published on 22 February, 2022.

Abstract

Trimetazidine dihydrochloride (TD) is an anti-ischemic drug that is used to effectively treat angina pectoris symptoms. During the manufacture of TD from gallic acid a process related impurity, pyrogallol, is produced. Up to the present time, no appropriate method has been proposed for the detection and analysis of pyrogallol in the TD at the level of threshold of toxicological concern. Therefore, in this investigation, a reliable and reproducible HPLC method was developed for the detection and analysis of pyrogallol in the TD. The method was validated in full compliance with the recommendations of the International Harmonization Council. Regression analysis indicated a correlation coefficient value of 0.9990 for pyrogallol between 6.3 ppm and 31.5 ppm. The LOD was 1.89 ppm and LOQ was 6.3 ppm for pyrogallol. Good recovery (accuracy) was observed in the range of 98.34% to 118.54% with an RSD value (precision) of 0.150%. Pyrogallol analysis in batches TD material has demonstrated the good performance of the method. The process is therefore useful in the identification and evaluation of pyrogallol content in drug substance of TD.

Keywords

Pyrogallol, Trimetazidine dihydrochloride, Process impurity, HPLC, Analysis