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dc.contributor.authorM J Akhtar-
dc.contributor.authorM Hafiz-
dc.contributor.authorS Khan-
dc.date.accessioned2023-01-23T09:50:16Z-
dc.date.available2023-01-23T09:50:16Z-
dc.date.issued1993-01-05-
dc.identifier.citationAkhtar, M. J., Khan, S., & Hafiz, M. (1994). High-performance liquid chromatographic assay for the determination of paracetamol, pseudoephedrine hydrochloride and triprolidine hydrochloride. Journal of pharmaceutical and biomedical analysis, 12(3), 379-382.en_US
dc.identifier.issn1011-601X-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/16641-
dc.description.abstractThe different UV absorption characteristics of paracetamol, pseudoephedrine hydrochloride and triprolidine hydrochloride have been used to facilitate their determination in pharmaceutical preparations by HPLC. The method developed involves isocratic, reversed-phase chromatography. A 'wavelength switching' programme is preferred to the use of a compromise wavelength for all three compounds. This gives reasonable UV responses despite widely different UV characteristics and concentrations of drugs. The limits of quantitation are found to be within 200-700 micrograms ml-1 for paracetamol, 24-84 micrograms ml-1 for pseudoephedrine HCl and 1.0-4.0 micrograms ml-1 for triprolidine HCl. The method performs well in terms of precision and accuracy as indicated by linear regression analysis.en_US
dc.language.isoenen_US
dc.publisherKarachi: Faculty of Pharmacy & Pharmaceutical Sciences University of Karachien_US
dc.titleHigh-performance liquid chromatographic assay for the determination of paracetamol, pseudoephedrine hydrochloride and triprolidine hydrochlorideen_US
dc.typeArticleen_US
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