Quantitative estimation of trimazolin hydrochloride in pharmaceutical preparation by RP-HPLC method

A sensitive and selective RP-HPLC method was developed and validated for the quantitative determination of trimazolin hydrochloride in nasal drops formulations. The mobile phase composition was water-acetonitrile (50:50, v/v) and the UV detection was carried out at 270 nm. Linearity range in the con...

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Main Authors: Savić Ivana M., Nikolić Goran S., Banković Vladimir M., Savić Ivan M.
Format: Article
Language:English
Published: Association of Chemical Engineers of Serbia 2009-01-01
Series:Hemijska Industrija
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/0367-598X/2009/0367-598X0902087S.pdf
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author Savić Ivana M.
Nikolić Goran S.
Banković Vladimir M.
Savić Ivan M.
author_facet Savić Ivana M.
Nikolić Goran S.
Banković Vladimir M.
Savić Ivan M.
author_sort Savić Ivana M.
collection DOAJ
description A sensitive and selective RP-HPLC method was developed and validated for the quantitative determination of trimazolin hydrochloride in nasal drops formulations. The mobile phase composition was water-acetonitrile (50:50, v/v) and the UV detection was carried out at 270 nm. Linearity range in the concentration range of 10 to 110 μg cm-3. The method was tested and validated for various parameters according to ICH guidelines. The detection and quantization limits were found to be 1.45 and 4.8 μg cm-3, respectively. The results demonstrated that the procedure for estimation of trimazolin hydrochloride in nasal drops formulations was accurate, precise and reproducible.
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spelling doaj.art-44bcee70cf0a44a1829aef658d58d2f82022-12-21T23:18:04ZengAssociation of Chemical Engineers of SerbiaHemijska Industrija0367-598X2009-01-01632879310.2298/HEMIND0902087SQuantitative estimation of trimazolin hydrochloride in pharmaceutical preparation by RP-HPLC methodSavić Ivana M.Nikolić Goran S.Banković Vladimir M.Savić Ivan M.A sensitive and selective RP-HPLC method was developed and validated for the quantitative determination of trimazolin hydrochloride in nasal drops formulations. The mobile phase composition was water-acetonitrile (50:50, v/v) and the UV detection was carried out at 270 nm. Linearity range in the concentration range of 10 to 110 μg cm-3. The method was tested and validated for various parameters according to ICH guidelines. The detection and quantization limits were found to be 1.45 and 4.8 μg cm-3, respectively. The results demonstrated that the procedure for estimation of trimazolin hydrochloride in nasal drops formulations was accurate, precise and reproducible.http://www.doiserbia.nb.rs/img/doi/0367-598X/2009/0367-598X0902087S.pdfTrimazolin hydrochlorideHPLCValidation
spellingShingle Savić Ivana M.
Nikolić Goran S.
Banković Vladimir M.
Savić Ivan M.
Quantitative estimation of trimazolin hydrochloride in pharmaceutical preparation by RP-HPLC method
Hemijska Industrija
Trimazolin hydrochloride
HPLC
Validation
title Quantitative estimation of trimazolin hydrochloride in pharmaceutical preparation by RP-HPLC method
title_full Quantitative estimation of trimazolin hydrochloride in pharmaceutical preparation by RP-HPLC method
title_fullStr Quantitative estimation of trimazolin hydrochloride in pharmaceutical preparation by RP-HPLC method
title_full_unstemmed Quantitative estimation of trimazolin hydrochloride in pharmaceutical preparation by RP-HPLC method
title_short Quantitative estimation of trimazolin hydrochloride in pharmaceutical preparation by RP-HPLC method
title_sort quantitative estimation of trimazolin hydrochloride in pharmaceutical preparation by rp hplc method
topic Trimazolin hydrochloride
HPLC
Validation
url http://www.doiserbia.nb.rs/img/doi/0367-598X/2009/0367-598X0902087S.pdf
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