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

被引:7
|
作者
Yelampalli, Suresh Reddy [1 ]
Gandla, Kumaraswamy [2 ]
Reddy, Konatham Teja Kumar [3 ]
Ibrahim, Adel Ehab [4 ,5 ]
El Deeb, Sami [4 ,6 ]
机构
[1] KL Univ, Dept Chem, Vijayawada 521333, India
[2] Chaitanya Deemed Univ, Dept Pharmaceut Anal, Hanamkonda 506144, India
[3] Univ Coll Technol, Dept Pharm, Osmania Univ Main Rd, Hyderabad 500007, India
[4] Univ Nizwa, Nat & Med Sci Res Ctr, Birkat Al Mauz, POB 33, Nizwa 616, Oman
[5] Port Said Univ, Fac Pharm, Pharmaceut Analyt Chem Dept, Port Said 42511, Egypt
[6] Tech Univ, Inst Med & Pharmaceut Chem, D-38092 Braunschweig, Germany
关键词
ion chromatography; sodium sulfate; potassium sulfate; magnesium sulfate; method validation; oral dosage form; ICP-MS; CALCIUM; WATER; TOOL;
D O I
10.3390/separations10020099
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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((R))IonPac((R)) CS16 column (250 x 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.
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页数:10
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