Red clover flowers are a rich source of isoflavones in the forms of biochanin A, formononetin, genistein, and genistin. A simple process was developed to recover isoflavones from red clover flowers as a nutraceutical product. Isoflavones were 1st extracted in alkaline water and insoluble polyvinylpolypyrrolidone (PVP) was then added to the extract for adsorbing isoflavones. The adsorbed isoflavones were subsequently eluted with ethanol and dried. The main steps of this process were optimized for the product yield and quality. The final product was an isoflavone concentrate, containing more than 20 wt% isoflavones, which represented a recovery of greater than 50% of the total isoflavone amount in red clover flowers.
Based on a lab-scale aqueous process for making skimmed soymilk, a membrane intensive scheme was developed to recover isoflavones as a separate product from the waste stream while soymilk was prepared as the main product. It was shown that, despite the protein binding, most extracted isoflavones permeated through the selected ultrafiltration membranes. Therefore, instead of solvents or adsorbents, a combination of ultrafiltration and diafiltration was used to separate isoflavones from the proteins and other bean components, and isoflavones were then concentrated by reverse osmosis. A yield of approximately 50% of the total amount of isoflavones in soybeans was eventually obtained in the reverse osmosis retentate, which could be dried to make an isoflavone supplement. With minor modifications, the process was readily adaptable to isoflavone recovery from soy protein processing with defatted soy flour. Crown
The effect of amphotericin B in an emulsion formulation on the integrity of monolayers of kidney cells has been studied. Whereas a conventional solubilized amphotericin formulation (Fungizone, Squibb) caused a loss in monolayer integrity at concentrations above 1 microgram mL-1, the emulsion formulation had no measurable effect on confluence at amphotericin concentrations up to 100 micrograms mL-1. The emulsion retained a comparable antifungal activity to that of Fungizone against Saccharomyces cerevisiae in suspension culture. These results parallel the observed erythrocyte lysis data obtained previously using amphotericin B emulsions, and suggest that the emulsion formulation may have a lower toxicity and improved therapeutic potential over existing formulations.
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