Evaluation of starches obtained from four dioscorea species as binding agent in chloroquine phosphate tablet formulations

dc.contributor.authorOkunlola, A.
dc.contributor.authorOdeku, O. A.
dc.date.accessioned2018-10-22T09:55:34Z
dc.date.available2018-10-22T09:55:34Z
dc.date.issued2011-01
dc.description.abstractStarches obtained from four Dioscorea species namely Dioscorea dumetorum (Bitter), Dioscorea oppositifolia (Chinese), Dioscorea alata (Water), and Dioscorea rotundata (White) have been evaluated as binding agents in chloroquine phosphate tablet formulations in comparison with official corn starch. The compressional properties of the formulations were analyzed using density measurements and the Heckel and Kawakita equations. The mechanical properties of the tablets were assessed using tensile strength, brittle fracture index (BFI), and friability tests while the drug release properties of the tablets were assessed using disintegration and dissolution times. The results indicate that the four starches vary considerably in their physicochemical properties. The ranking for the tensile strength and the disintegration and dissolution times for the formulations was Chinese> Bitter > Corn> White > Water while the ranking was reversed for BFI and friability. The results suggest that Water, White, and Corn could be useful when faster disintegration time of tablets is desired while Chinese and Bitter could be more useful when bond strength is of concern and in minimizing the problems of lamination and capping in tablet formulationen_US
dc.identifier.issn1319-0164
dc.identifier.otherui_art_okunola_evaluation
dc.identifier.otherSaudi Pharmaceutical Journal 19, pp. 95-105
dc.identifier.urihttp://ir.library.ui.edu.ng/handle/123456789/3448
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectStarchen_US
dc.subjectYamen_US
dc.subjectDioscorea speciesen_US
dc.subjectCorn starchen_US
dc.subjectBinding agenten_US
dc.titleEvaluation of starches obtained from four dioscorea species as binding agent in chloroquine phosphate tablet formulationsen_US
dc.typeArticleen_US

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