Determination of ibuprofen by high performance liquid chromatography

Ibuprofen in its pure form and in pharmaceutical formulations (tablets and suspension-dose forms) was determined by high-performance liquid chromatography (HPLC). The analysis was performed on a C18 column (3.9 mm × 150 mm, 5 μm) with a mobile phase consisting of methanol-water-phosphoric acid in ratios [75:24.7:0.3] respectively, and a flow rate of 0.8 mL/min. A UV detector with a wavelength of 214 nm was used. The results were linear in the range of 3,125-100,000 μg/mL for ibuprofen. Correlation coefficients were R = 0.999993 The relative standard deviations (n = 6) for the daytime assay and the inter-day assay were 0.152%, 0.382% This method was characterized by high precision and accuracy and is suitable for quality control in the pharmaceutical industries.

Authors

Publication Details

Journal
International Journal of Science and Research Archive
Published
2025-02-21
DOI
https://doi.org/10.30574/ijsra.2025.14.2.0519
Primary Topic
Analytical Chemistry and Chromatography
Type
article
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article

Determination of ibuprofen by high performance liquid chromatography

Mohammed Nawfal Abdul Mageda, Amal H. Mehmed, Hussein Ali Al-Bahrania
International Journal of Science and Research Archive
Analytical Chemistry and Chromatography
article

Determination of ibuprofen by high performance liquid chromatography

Mohammed Nawfal Abdul Mageda, Amal H. Mehmed, Hussein Ali Al-Bahrania
article en

Abstract

Ibuprofen in its pure form and in pharmaceutical formulations (tablets and suspension-dose forms) was determined by high-performance liquid chromatography (HPLC). The analysis was performed on a C18 column (3.9 mm × 150 mm, 5 μm) with a mobile phase consisting of methanol-water-phosphoric acid in ratios [75:24.7:0.3] respectively, and a flow rate of 0.8 mL/min. A UV detector with a wavelength of 214 nm was used. The results were linear in the range of 3,125-100,000 μg/mL for ibuprofen. Correlation coefficients were R = 0.999993 The relative standard deviations (n = 6) for the daytime assay and the inter-day assay were 0.152%, 0.382% This method was characterized by high precision and accuracy and is suitable for quality control in the pharmaceutical industries.

International Journal of Science and Research ArchiveVol. 14(2)
Openalex Percentile: Top 97%
Analytical Chemistry and Chromatography
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