The mechanism of antimalarial action of [Au(CQ)(PPh₃)]PF₆: Structural effects and increased drug lipophilicity enhance heme aggregation inhibition at lipid/water interfaces

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• 作者：Maribel Navarro^a ; ^{mnavarro@ivic.ve} ; ^{maribelnava@gmail.com} ; William Castro^a ; Alberto Mart&#xed ; nez^b ; Roberto A. Sá ; nchez Delgado^b
• 关键词：Malaria ; Resistance ; Plasmodium falciparum ; Chloroquine ; Gold ; β ; -Hematin ; Partition coefficient ; DNA
• 刊名：Journal of Inorganic Biochemistry
• 出版年：2011
• 出版时间：February 2011
• 年：2011
• 卷：105
• 期：2
• 页码：276-282
• 全文大小：398 K

文摘

The mechanism of antimalarial action of [Au(CQ)(PPh₃)]PF₆ (1), which is active in vitro against CQ-resistant P. falciparum and in vivo against P. berghei, has been investigated in relation to hemozoin formation and DNA as possible important targets. Complex 1 interacts with heme and inhibits β-hematin formation both in aqueous medium and near water/n-octanol interfaces at pH ~ 5 to a greater extent than chloroquine diphosphate (CQDP) or other known metal-based antimalarial agents; the higher inhibition activity is probably related to the higher lipophilicity observed for 1 through partition coefficient measurements at low pH, with respect to CQDP. The interactions of complex 1 with DNA were explored using spectrophotometric and fluorimetric titrations, circular dichroism spectroscopy, viscosity and melting point studies, as well as electrophoresis and covalent binding assays. The experimental data indicate that complex 1 interacts with DNA predominantly by intercalation and electrostatic association of the CQ moiety, similarly to free CQDP, while no covalent metal–DNA binding seems to take place. The most likely antimalarial mechanism for complex 1 is thus heme aggregation inhibition; the high activities observed against resistant parasites are probably due to the structural modification of CQ introduced by the presence of the gold-triphenylphosphine fragment, together with the enhanced lipophilic character.