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Stability of cyanocobalamin in parenteral preparations

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dc.contributor.author I Ahmad
dc.contributor.author W Hussain
dc.date.accessioned 2023-01-23T09:50:54Z
dc.date.available 2023-01-23T09:50:54Z
dc.date.issued 1993-01-08
dc.identifier.citation Ahmad, I., & Hussain, W. (1993). Stability of cyanocobalamin in parenteral preparations. Pakistan Journal of Pharmaceutical Sciences, 6(1), 53-59. en_US
dc.identifier.issn 1011-601X
dc.identifier.uri http://142.54.178.187:9060/xmlui/handle/123456789/16644
dc.description.abstract The stability of seven commercial parenteral preparations of cyanocobalamin (vitamin B(12)) on storage under normal laboratory conditions for a period of twelve months has been studied using a two component spectrophotometric method for the simultaneous determination of cyanocobalamin and the degradation product, hydroxocobalamin, at 550 and 525 nm. The single ingredient vitamin B(12) preparations have been found to be stable and the potency lies within the B.P. limits. In multi-ingredient (B(1) + B(6) + B(12)) preparations cyanocobalamin is unstable and degrades from 28% to 37% with concomitant formation of hydroxocobalamin (1.7% to 25.5%) and oxidation products amounting to 56.4% +/- 9.3. Thus more than half of the vitamin content is lost during storage and these preparations are not suitable for parenteral use. en_US
dc.language.iso en en_US
dc.publisher Karachi: Faculty of Pharmacy & Pharmaceutical Sciences University of Karachi en_US
dc.title Stability of cyanocobalamin in parenteral preparations en_US
dc.type Article en_US


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