Determination of Atenolol and Hydrochlorothiazide in Pharmaceutical Preparation Using RP-HPLC

Authors

  • Saad Antakli
  • Leon Nejem
  • Moustafa Alabo Joumaa

Keywords:

HPLC
Atenolol
Hydrochlorothiazide

Abstract

A (Reversed Phase High Performance Liquid Chromatography) (RP-HPLC) method was Development for the determination of Atenolol (ATE) and Hydrochlorothiazide (HCT) in tablets formulations. Isocratic Elution Chromatography analysis was achieved with (methanol: phosphoric acid) (pH = 4) in ratio of 70:30 (v/v) as mobile phase, the analytical is done by C18 column and UV detector at 220 nm, pump flow rate was 1.2 mL/min and sample injection volume 20 μL.

The proposed method was successfully applied to analysis individual or mixture of (ATE) and (HCT) in Syrian trademark drugs. All studied samples showed that the drug levels were conformed to British Pharmacopeia. Finally, the method is simple, selective and suitable for routine quality control analysis.

Author Biographies

Saad Antakli

Faculty of Science | University of Aleppo | Syria

Leon Nejem

Faculty of Science | University of Aleppo | Syria

Moustafa Alabo Joumaa

Faculty of Science | University of Aleppo | Syria

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Published

2022-09-28

How to Cite

1.
Determination of Atenolol and Hydrochlorothiazide in Pharmaceutical Preparation Using RP-HPLC. JNSLAS [Internet]. 2022 Sep. 28 [cited 2024 Aug. 25];6(3):144-52. Available from: https://journals.ajsrp.com/index.php/jnslas/article/view/5621

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How to Cite

1.
Determination of Atenolol and Hydrochlorothiazide in Pharmaceutical Preparation Using RP-HPLC. JNSLAS [Internet]. 2022 Sep. 28 [cited 2024 Aug. 25];6(3):144-52. Available from: https://journals.ajsrp.com/index.php/jnslas/article/view/5621