Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/3152
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dc.contributor.authorPatel, Pranav-
dc.contributor.authorPanchal, Shital J.-
dc.contributor.authorMehta, Tejal A.-
dc.date.accessioned2012-04-21T05:00:20Z-
dc.date.available2012-04-21T05:00:20Z-
dc.date.issued2011-
dc.identifier.urihttp://10.1.7.181:1900/jspui/123456789/3152-
dc.descriptionInternational Journal of Pharmacy and Pharmaceutical sciences 9(4):220-222, 2011en_US
dc.description.abstractAn accurate, simple, and reproducible liquid chromatographic method was developed and validated for the determination of Tacrolimus in capsules. The analysis was performed at ambient temperature on a reversed-phase C18 column with UV detection at 213 nm. The mobile phase was acetonirile (100 %) used at a constant flow rate of 0.9 ml/min. The method was validated in terms of linearity, precision, accuracy, and specificity .The response was linear in the range of 5-250 μg/ml (r2= 0.9978). The relative standard deviations for intra- and inter-day precision studies were found to be less than 2% with 98.90 to 101.12% accuracy, respectively.en_US
dc.publisherInternational Journal of Pharmacy and Pharmaceutical sciencesen_US
dc.relation.ispartofseriesIPFP0059en_US
dc.subjectTacrolimusen_US
dc.subjectRP-HPLCen_US
dc.subjectFaculty Paperen_US
dc.subjectPharmacy Faculty Paperen_US
dc.titleReversed-Phase high performance liquid chromatographic (RP_HPLC) method for determination of tacrolimus in bulk and pharmaceutical formulationen_US
dc.typeFaculty Papersen_US
Appears in Collections:Faculty Papers

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