Determination of Sodium, Potassium, and Magnesium as Sulfate Salts in Oral Preparations Using Ion Chromatography and Conductivity Detection

Author:

Yelampalli Suresh Reddy1ORCID,Gandla Kumaraswamy2,Reddy Konatham Teja Kumar3,Ibrahim Adel Ehab45ORCID,El Deeb Sami46ORCID

Affiliation:

1. Department of Chemistry, K.L. University, Vijayawada 521333, India

2. Department of Pharmaceutical Analysis, Chaitanya (Deemed to Be University), Hanamkonda 506144, India

3. Department of Pharmacy, University College of Technology, Osmania University Main Road, Amberpet, Hyderabad 500007, India

4. Natural and Medical Sciences Research Center, University of Nizwa, Birkat Al Mauz, P.O. Box 33, Nizwa 616, Oman

5. Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Port-Said University, Port-Said 42511, Egypt

6. Institute of Medicinal and Pharmaceutical Chemistry, Technische Universitaet, 38092 Braunschweig, Germany

Abstract

An ion chromatography technique with conductivity detection was selected as an analytical tool for the simultaneous indirect determination of sodium sulfate, potassium sulfate, and magnesium sulfate via their respective cations. The method was developed and validated for the quantitative assay of the inorganic salts under study in oral pharmaceutical dosage forms. Chromatographic separation was achieved on a Dionex®IonPac® CS16 column (250 × 5 mm) column using the gradient elution method. A mobile phase-A consisting of methane sulfonic acid (6.7%, v/v) in Milli-Q water, which is used together with Milli-Q water, was used as a mobile Phase-B. The flow rate was 1.2 mL/min. The retention times of sodium, potassium, and magnesium as sulfates were 7.8, 12.8, and 16.2 min, respectively. The method was validated according to ICH guidelines and showed good linearity and accuracy results within concentration ranges of 80.0–240.0, 20.0–60.0, and 4.5–13.5 ppm for sodium, potassium, and magnesium as sulfates, respectively. The relative standard deviation results for intra- and inter-day precision were less than 1.0%. The method was applied successfully for determination of the analytes under study in their mixed pharmaceutical oral solution and found suitable for their routine and stability analysis.

Publisher

MDPI AG

Subject

Filtration and Separation,Analytical Chemistry

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