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Dutch and Spanish team to take heart health fruit extract to the Americas

By Shane Starling , 17-Jan-2014
Last updated on 17-Jan-2014 at 13:15 GMT2014-01-17T13:15:17Z

“Parties have completed a pharmacokinetics study showing the high bioavailability of CordiArt...

“Parties have completed a pharmacokinetics study showing the high bioavailability of CordiArt..."

Two European firms have joined to take a citrus fruit extract into American markets backed by as yet unpublished science showing blood circulation benefits.

Spanish polyphenol specialist FerrerHealthTech will manufacture the fruit extract called CordiArt for Dutch player BioActor.

A BioActor spokesperson told us a study that showed blood circulation benefits in humans when 500mg of its Cordiart supplement was taken daily was in the process of being published by a peer review journal.

“Parties have completed a pharmacokinetics study showing the high bioavailability of CordiArt,” the companies said, noting a, robust research programme” was underway at least another three studies.

They are also taking part in the European Union BACCHUS Project that is investigating cardiovascular benefits from food components. There are 28 partners in that 4-year project including 16 Small and Medium Enterprises (SME) from 11 countries, led by the Institute of Food Research (IFR) in the UK.

“BioActor’s scientific excellence and intellectual property perfectly complements FerrerHealthTech’s expertise in polyphenols,” said Tom D’hoore, area manager of FerrerHealthTech. “Moreover, the agreement strengthens our value proposition to our customers in North and South America.”

The companies said CordiArt stimulates the eNOS-enzyme which is involved in the synthesis of nitric oxide, and important for vascular elasticity.

The CordiArt website states: Three weeks of intervention with 500 mg/day of CORDIART resulted in a better response of the arteries to changes in blood flow. Subjects who received 500 mg/day of CORDIART showed a 25% higher FMD (Flow Mediated Dilation)-score compared to subjects who received a placebo.”

“This results is clinically relevant as the treated group reached an FMD-score of >10, which is considered ‘healthy’, whilst the placebo group showed the hallmark of endothelial dysfunction. FMD scores of <10 are already sufficient to predict adverse cardiovascular events in otherwise healthy subjects.”

But the claims are not backed as yet under the EU nutrition and health claims regulation (NHCR). 

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