A Review on Various Analytical Method Development and Validation for Simultaneous Estimation of Levo-Salbutamol and Ipratropium Bromide in Bulk and Pharmaceutical Dosage Form by RP-HPLC

For the simultaneous measurement of levosalbutamol and ipratropium bromide, a quick and sensitive reverse phase high performance liquid chromatography (RP-HPLC) approach has been devised. Chromatographic separation was accomplished using a mobile phase made up of 0.01M potassium dihydrogen phosphate and ethanol (pH was corrected to 3.0 using O-phosphoric acid) on a reverse phase Enable C18 column (250 X 4.6 mm, 5 µm). A UV detector set to 245 nm was used for detection after the mobile phase was pumped at a flow rate of 1.0 ml/min. The suggested approach could be used for routine quality control analysis for the simultaneous determination of levosalbutamol and ipratropium bromide in pharmaceutical dosage forms since it was found to be easy to use, quick, accurate, precise, and repeatable.

Authors

Publication Details

Journal
International Journal of Research in Pharmacy and Allied Science
Published
2025-01-01
DOI
https://doi.org/10.71431/ijrpas.2025.4904
Primary Topic
Analytical Methods in Pharmaceuticals
Type
article
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article

A Review on Various Analytical Method Development and Validation for Simultaneous Estimation of Levo-Salbutamol and Ipratropium Bromide in Bulk and Pharmaceutical Dosage Form by RP-HPLC

T. Rama Rao, M. Sangeetha, U. Akhila
International Journal of Research in Pharmacy and Allied Science
Analytical Methods in Pharmaceuticals
article

A Review on Various Analytical Method Development and Validation for Simultaneous Estimation of Levo-Salbutamol and Ipratropium Bromide in Bulk and Pharmaceutical Dosage Form by RP-HPLC

T. Rama Rao, M. Sangeetha, U. Akhila
article en

Abstract

For the simultaneous measurement of levosalbutamol and ipratropium bromide, a quick and sensitive reverse phase high performance liquid chromatography (RP-HPLC) approach has been devised. Chromatographic separation was accomplished using a mobile phase made up of 0.01M potassium dihydrogen phosphate and ethanol (pH was corrected to 3.0 using O-phosphoric acid) on a reverse phase Enable C18 column (250 X 4.6 mm, 5 µm). A UV detector set to 245 nm was used for detection after the mobile phase was pumped at a flow rate of 1.0 ml/min. The suggested approach could be used for routine quality control analysis for the simultaneous determination of levosalbutamol and ipratropium bromide in pharmaceutical dosage forms since it was found to be easy to use, quick, accurate, precise, and repeatable.

International Journal of Research in Pharmacy and Allied ScienceVol. 04(09)
Openalex Percentile: Top 68%
Analytical Methods in Pharmaceuticals
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