Andrographolide: Solving chemical instability and poor solubility by means of cocrystals

dc.contributor.author Suresh, Kuthuru
dc.contributor.author Goud, N. Rajesh
dc.contributor.author Nangia, Ashwini
dc.date.accessioned 2022-03-27T09:25:36Z
dc.date.available 2022-03-27T09:25:36Z
dc.date.issued 2013-12-01
dc.description.abstract The bioactive agent andrographolide was screened with pharmaceutically acceptable coformers to discover a novel solid form that will solve the chemical instability and poor solubility problems of this herbal medicine. Liquid-assisted grinding of andrographolide with GRAS (generally regarded as safe) coformers in a fixed stoichiometry resulted in cocrystals with vanillin (1:1), vanillic acid (1:1), salicylic acid (1:1), resorcinol (1:1), and guaiacol (1:1). All the crystalline products were characterized by thermal, spectroscopic, and diffraction methods. Interestingly, even though the cocrystals are isostructural, their physicochemical properties are quite different. The andrographolide-salicylic acid cocrystal completely inhibited the chemical transformation of andrographolide to its inactive sulfate metabolite, and moreover, the cocrystal exhibited a dissolution rate that was three times faster and a drug release that was two times higher than pure andrographolide. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
dc.identifier.citation Chemistry - An Asian Journal. v.8(12)
dc.identifier.issn 18614728
dc.identifier.uri 10.1002/asia.201300859
dc.identifier.uri https://onlinelibrary.wiley.com/doi/10.1002/asia.201300859
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12889
dc.subject crystal engineering
dc.subject isostructurality
dc.subject medicinal chemistry
dc.subject natural products
dc.subject X-ray diffraction
dc.title Andrographolide: Solving chemical instability and poor solubility by means of cocrystals
dc.type Journal. Article
dspace.entity.type
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