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Please use this identifier to cite or link to this item: http://142.54.178.187:9060/xmlui/handle/123456789/16392
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dc.contributor.authorKamal Shah-
dc.contributor.authorSushant K-
dc.contributor.authorShrivastava-
dc.contributor.authorPradeep Mishra-
dc.date.accessioned2023-01-20T07:28:55Z-
dc.date.available2023-01-20T07:28:55Z-
dc.date.issued2014-07-25-
dc.identifier.citationShah, K., Shrivastava, S. K., & Mishra, P. (2014). Formulation and evaluation of suspensions: Mefenamic acid prodrugs. Pakistan journal of pharmaceutical sciences, 27(4).en_US
dc.identifier.issn1011-601X-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/16392-
dc.description.abstractGastrosparing novel prodrugs (MAM and MAT) synthesized consisted of mefenamic acid (MA) with menthol (M) and thymol (T). Structural characterizations of synthesized esters were done by Infra red spectroscopy (IR), proton nuclear magnetic resonance (1 HNMR), mass spectroscopy. After evaluation of pharmacological i.e. anti-inflammatory, analgesic and ulcerogenic activities, the preformulation studies were undertaken. Based on these a few formulation (suspensions) were designed and prepared. The formulated suspensions were evaluated for content uniformity, sedimentation volume, recovery studies, redispersibility, viscosity, pH, particle size, zeta potential, effect of temperature and in-vitro dissolution rate. All the above parameters were found to be within the limit these indicated that the synthesized esters are good candidate for liquid dosage form. Thus it can be concluded synthesized prodrugs can be formulated in suspension form.en_US
dc.language.isoenen_US
dc.publisherKarachi: Faculty of Pharmacy, University of Karachien_US
dc.subjectMutual prodrugen_US
dc.subjectmefenamic aciden_US
dc.subjectsuspensions, dissolutionen_US
dc.subjectpreformulationen_US
dc.titleFormulation and evaluation of suspensions: Mefenamic acid prodrugsen_US
dc.typeArticleen_US
Appears in Collections:Issue No.4

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