Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/9975
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dc.contributor.authorPrajapati, Pintu B.-
dc.contributor.authorWankhed, Navneet-
dc.contributor.authorMehta, Priti J.-
dc.date.accessioned2021-08-16T10:27:12Z-
dc.date.available2021-08-16T10:27:12Z-
dc.date.issued2019-
dc.identifier.urihttp://10.1.7.192:80/jspui/handle/123456789/9975-
dc.descriptionJournal of Drug Delivery & Therapeutics. 2019; 9(4-A):793-802en_US
dc.description.abstractInternational Conference on Harmonization (ICH) has formulated different guideline regarding the control of impurities. In this review, the impurity sources, classification, isolation, detection and characterization methods are described. The some impurities are unavoidable and will be present in trace amounts hence ICH guidelines frame the different policies and establish the specification limits, isolation and characterization is necessary for evaluation and control of impurities. The other regulatory bodies and drug development authorities look up to these guidelines for launching a quality drug into the market. Validation of analytical process for impurity identification is performed to establish the impurity profile of any drug substance. Hence the major focus of this review article is on isolation and characterization of impurities using various technics, sources and classifications, establishment of impurity profile and analytical approaches to establish its profile. We also could apply the QbD to providing statistical documentary evidencesen_US
dc.publisherSociety of Pharmaceutical Technocratsen_US
dc.relation.ispartofseriesIPFP0417;-
dc.subjectImpurity profileen_US
dc.subjectImpurities isolation methodsen_US
dc.subjectchromatographic separationen_US
dc.subjectImpurity Characterizationen_US
dc.subjectICHen_US
dc.subjectQbDen_US
dc.titleA Review on Multi Approaches for Impurity Isolation and its Characterizationen_US
dc.typeFaculty Papersen_US
Appears in Collections:Faculty Papers

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