sharon sanders
Editor-in-Chief & President
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<!-- <rdf:RDF xmlns:cc="http://web.resource.org/cc/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns
rism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns="http://purl.org/rss/1.0/"> <cc:Work rdf:about="http://www.malariajournal.com/content/6/1/81"> <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/> </cc:Work> <cc:License rdf:about="http://creativecommons.org/licenses/by/2.0/"> <ccermits rdf:resource="http://web.resource.org/cc/Reproduction"/> <ccermits rdf:resource="http://web.resource.org/cc/Distribution"/> <cc:requires rdf:resource="http://web.resource.org/cc/Notice"/> <cc:requires rdf:resource="http://web.resource.org/cc/Attribution"/> <ccermits rdf:resource="http://web.resource.org/cc/DerivativeWorks"/> </cc:License> <item rdf:about="http://www.malariajournal.com/content/6/1/81"> <title>In vitro activity of ferroquine (SSR 97193) against Plasmodium falciparum isolates from the Thai-Burmese border</title> <dc:title>In vitro activity of ferroquine (SSR 97193) against Plasmodium falciparum isolates from the Thai-Burmese border</dc:title> <dc:creator>Barends, Marion</dc:creator> <dc:creator>Jaidee, Anchailee</dc:creator> <dc:creator>Khaohirun, Nopparat</dc:creator> <dc:creator>Singhasivanon, Pratap</dc:creator> <dc:creator>Nosten, Francois</dc:creator> <dc:identifier>info:doi/10.1186/1475-2875-6-81</dc:identifier> <dc:source>Malaria Journal 2007, 6:81</dc:source> <dc:date>2007-06-27</dc:date>
Malaria Journal</prismublicationName>
2007-06-27</prismublicationDate>
6</prism:volume>
1</prism:number>
Case study</prism:section>
81</prism:startingPage> </item> </rdf:RDF> -->.</td> </tr> </tbody></table>In vitro activity of ferroquine (SSR 97193) against Plasmodium falciparum isolates from the Thai-Burmese border
Marion Barends
, Anchailee Jaidee , Nopparat Khaohirun , Pratap Singhasivanon and Francois Nosten
Malaria Journal 2007, 6:81 doi:10.1186/1475-2875-6-81
<table class="smalltext" cellpadding="0" cellspacing="0"><tbody><tr> <td>Published</td> <td width="25"> </td> <td>27 June 2007</td> </tr> </tbody></table>
Abstract (provisional)
The complete article is available as a provisional PDF. The fully formatted PDF and HTML versions are in production.
Background
On the borders of Thailand, Plasmodium falciparum has become resistant to nearly all available drugs, and there is an urgent need to find new antimalarial drugs or drug combinations. Ferroquine (SSR97193) is a new 4-aminoquinoline antimalarial active against chloroquine resistant and sensitive P. falciparum strains in vivo and in vitro. This antimalarial organic iron complex (a ferrocenyl group has been associated with chloroquine) is meant to use the affinity of Plasmodium for iron to increase the probability for encountering the anti-malarial molecule. The aim of the present study was to investigate the activity of ferroquine against P. falciparum isolates from an area with a known high multi-drug resistance rate.
Methods
Parasite isolates were obtained from patients with acute falciparum malaria attending the clinics of SMRU. In vitro cultures of these isolates were set-up in the SMRU-laboratory on pre-dosed drug plates, and grown in culture for 42 hours. Parasite growth was assessed by the double-site enzyme-linked pLDH immunodetection (DELI) assay.
Results
Sixty-five P. falciparum isolates were successfully grown in culture. The ferroquine mean IC50 (95% CI) was 9.3 nM (95% C.I.: 8.7 - 10.0). The mean IC50 value for the principal metabolite of ferroquin, SR97213A, was 37.0 nM (95% C.I.: 34.3 - 39.9), which is four times less active than ferroquine. The isolates in this study were highly multi-drug resistant but ferroquine was more active than chloroquine, quinine, mefloquine and piperaquine. Only artesunate was more active than ferroquine. Weak but significant correlations were found between ferroquine and its principal metabolite (r2 = 0.4288), chloroquine (r2 = 0.1107) and lumefantrine (r2 = 0.2364).
Conclusion
The results presented in this study demonstrate that the new ferroquine compound SSR97193 has high anti-malarial activity in vitro against multi-drug resistant P. falciparum.
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<!-- <rdf:RDF xmlns:cc="http://web.resource.org/cc/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlnsrism="http://prismstandard.org/namespaces/1.2/basic/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns="http://purl.org/rss/1.0/"> <cc:Work rdf:about="http://www.malariajournal.com/content/6/1/81"> <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/"/> </cc:Work> <cc:License rdf:about="http://creativecommons.org/licenses/by/2.0/"> <ccermits rdf:resource="http://web.resource.org/cc/Reproduction"/> <ccermits rdf:resource="http://web.resource.org/cc/Distribution"/> <cc:requires rdf:resource="http://web.resource.org/cc/Notice"/> <cc:requires rdf:resource="http://web.resource.org/cc/Attribution"/> <ccermits rdf:resource="http://web.resource.org/cc/DerivativeWorks"/> </cc:License> <item rdf:about="http://www.malariajournal.com/content/6/1/81"> <title>In vitro activity of ferroquine (SSR 97193) against Plasmodium falciparum isolates from the Thai-Burmese border</title> <dc:title>In vitro activity of ferroquine (SSR 97193) against Plasmodium falciparum isolates from the Thai-Burmese border</dc:title> <dc:creator>Barends, Marion</dc:creator> <dc:creator>Jaidee, Anchailee</dc:creator> <dc:creator>Khaohirun, Nopparat</dc:creator> <dc:creator>Singhasivanon, Pratap</dc:creator> <dc:creator>Nosten, Francois</dc:creator> <dc:identifier>info:doi/10.1186/1475-2875-6-81</dc:identifier> <dc:source>Malaria Journal 2007, 6:81</dc:source> <dc:date>2007-06-27</dc:date> Malaria Journal</prism
ublicationName> 2007-06-27</prism
ublicationDate> 6</prism:volume>
1</prism:number>
Case study</prism:section>
81</prism:startingPage> </item> </rdf:RDF> -->.</td> </tr> </tbody></table>In vitro activity of ferroquine (SSR 97193) against Plasmodium falciparum isolates from the Thai-Burmese border
Marion Barends
, Anchailee Jaidee , Nopparat Khaohirun , Pratap Singhasivanon and Francois Nosten Malaria Journal 2007, 6:81 doi:10.1186/1475-2875-6-81
<table class="smalltext" cellpadding="0" cellspacing="0"><tbody><tr> <td>Published</td> <td width="25"> </td> <td>27 June 2007</td> </tr> </tbody></table>
Abstract (provisional)
The complete article is available as a provisional PDF. The fully formatted PDF and HTML versions are in production.
Background
On the borders of Thailand, Plasmodium falciparum has become resistant to nearly all available drugs, and there is an urgent need to find new antimalarial drugs or drug combinations. Ferroquine (SSR97193) is a new 4-aminoquinoline antimalarial active against chloroquine resistant and sensitive P. falciparum strains in vivo and in vitro. This antimalarial organic iron complex (a ferrocenyl group has been associated with chloroquine) is meant to use the affinity of Plasmodium for iron to increase the probability for encountering the anti-malarial molecule. The aim of the present study was to investigate the activity of ferroquine against P. falciparum isolates from an area with a known high multi-drug resistance rate.
Methods
Parasite isolates were obtained from patients with acute falciparum malaria attending the clinics of SMRU. In vitro cultures of these isolates were set-up in the SMRU-laboratory on pre-dosed drug plates, and grown in culture for 42 hours. Parasite growth was assessed by the double-site enzyme-linked pLDH immunodetection (DELI) assay.
Results
Sixty-five P. falciparum isolates were successfully grown in culture. The ferroquine mean IC50 (95% CI) was 9.3 nM (95% C.I.: 8.7 - 10.0). The mean IC50 value for the principal metabolite of ferroquin, SR97213A, was 37.0 nM (95% C.I.: 34.3 - 39.9), which is four times less active than ferroquine. The isolates in this study were highly multi-drug resistant but ferroquine was more active than chloroquine, quinine, mefloquine and piperaquine. Only artesunate was more active than ferroquine. Weak but significant correlations were found between ferroquine and its principal metabolite (r2 = 0.4288), chloroquine (r2 = 0.1107) and lumefantrine (r2 = 0.2364).
Conclusion
The results presented in this study demonstrate that the new ferroquine compound SSR97193 has high anti-malarial activity in vitro against multi-drug resistant P. falciparum.