Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/7098
Full metadata record
DC FieldValueLanguage
dc.contributor.authorBasavaiah, K-
dc.contributor.authorRamakrishna, V-
dc.contributor.authorKumar, U R Anil-
dc.contributor.authorKumar, Udaya-
dc.date.accessioned2010-01-07T06:43:50Z-
dc.date.available2010-01-07T06:43:50Z-
dc.date.issued2006-11-
dc.identifier.issn0975-0991 (Online); 0971-457X (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/7098-
dc.description549-554en_US
dc.description.abstractTwo rapid assay procedures based on visible spectrophotometry and high performance liquid chromatography (HPLC) have been developed for lansoprazole in bulk drug and in capsules. Spectrophotometric method is based on the formation of a charge-transfer (CT) complex between chloranilic acid (CAA) as a -acceptor and lansoprazole (LPZ) as an n-donor in acetonitrile solvent, the absorbance of the complex being measured at 520 nm. Beer’s law is obeyed for 5-80 g mL-1 with an apparent molar absorptivity of 3.45103 L mol-1 cm-1 and a Sandell sensitivity of 0.0011 µg cm2-. The HPLC determination was performed on a reversed phase column (Hypersil C18 5 µm; 2504.6 m, i.d) using a mobile phase (1 mL min-1) consisting of acetonitrile-0.1% phosphoric acid (pH 3)-70:30(v/v) with UV-detection at 284 nm. A reactilinear relationship between mean peak area and concentration of LPZ was observed in the range 6-248 g mL-1 with a detection limit of 0.62 g mL-1 and a quantitation limit of 1.86 g mL-1. Intra-day and inter-day precision, and accuracy of the methods have been established according to the current ICH guidelines. The methods have been successfully applied to the assay of LPZ in tablet preparations with recoveries varying from 97.14 to 102.3% with standard deviation in the range of 0.57-1.65%. The results were statistically compared with those of the reference method by applying Student’s t-test and F-test. Accuracy, evaluated by means of the spike recovery method was in the range 97.66-106.6%, with precision (RSD) better than 3%.en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesB01D15/00en_US
dc.sourceIJCT Vol.13(6) [November 2006]en_US
dc.subjectLansoprazoleen_US
dc.subjectAssayen_US
dc.subjectSpectrophotometryen_US
dc.subjectHPLCen_US
dc.subjectChloranilic aciden_US
dc.titleSpectrophotometric and high performance liquid-chromatographic determination of lansoprazole in pharmaceuticalsen_US
dc.typeArticleen_US
Appears in Collections:IJCT Vol.13(6) [November 2006]

Files in This Item:
File Description SizeFormat 
IJCT 13(6) 549-554.pdf149.19 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.