Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2041
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dc.contributor.authorGupta, Vijay-
dc.contributor.authorMandal, S.K.-
dc.date.accessioned2020-11-23T06:27:45Z-
dc.date.available2020-11-23T06:27:45Z-
dc.date.issued2018-
dc.identifier.citationJournal of Pharmaceutical and Biomedical Analysis, 153, pp. 102-109en_US
dc.identifier.otherhttps://doi.org/10.1016/j.jpba.2018.02.006-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0731708517325347-
dc.identifier.urihttp://hdl.handle.net/123456789/2041-
dc.descriptionOnly IISERM authors are available in the record.-
dc.description.abstractThe present work highlights a novel polymorph (form II) of ambrisentan (AMT), a selective endothelin type A (ETA) receptor antagonist used in the treatment of pulmonary arterial hypertension (PAH). Form II was isolated by solution crystallization and characterised by differential scanning calorimetry, powder X-ray diffraction, solution calorimetry and aqueous solubility. The single crystal X-ray diffraction shows that it crystallizes in monoclinic system with space group P21/c different from the form I (commercial form). Form II was found to be enantiotropically related to form I. Apparent solubility of form II was performed in 0.1 N HCl (pH 1.2) was found to be higher (1.5 fold) than of form I. Solution mediated and stress-induced phase transformation studies revealed conversion of form II to form I. Accelerated stability studies (40 °C & 75% RH) also reveal that form II converted to form I after one month. However, this does not belittle the improved solubility of a new solid form.en_US
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.subjectPolymorphsen_US
dc.subjectPhase transformationen_US
dc.subjectSolution crystallizationen_US
dc.subjectSolubilityen_US
dc.subjectSolution calorimetryen_US
dc.titleNovel polymorph of ambrisentan: Characterization and stabilityen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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