Abstrak
Antiplasmodial properties of kaempferol-3-O-rhamnoside isolated from the leaves of Schima wallichii against chloroquine-resistant Plasmodium falciparum
Melisa I. Barliana, Eka W. Suradji, Rizky Abdulah, Ajeng Diantini, Toshimitsu Hatabu, Junko Nakajima-Shimada, Anas Subarnas, Hiroshi Koyama
Universitas Padjadjaran, Biomedical Reports 2: 579-583 April 15, 2014, Doi: 10.3892/Br.2014.271
Bahasa Inggris
Universitas Padjadjaran, Biomedical Reports 2: 579-583 April 15, 2014, Doi: 10.3892/Br.2014.271
antiplasmodial, malaria, medicinal plant, natural product, primates
Previous intervention studies have shown that the most effective agents used in the treatment of malaria were isolated from natural sources. Plants consumed by non-human primates serve as potential drug sources for human disease management due to the similarities in anatomy, physiology and disease characteristics. The present study investigated the anti¬plasmodial properties of the primate-consumed plant, Schima wallichii (S. wallichii) Korth. (family Theaceae), which has already been reported to have several biological activities. The ethanol extract of S. wallichii was fractionated based on polarity using n-hexane, ethyl acetate and water. The antiplas¬modial activity was tested in vitro against chloroqui ne-resistant Plasmodium falciparum (P. falciparum) at 100 ug/ml for 72 h. The major compound of the most active ethyl acetate fraction was subsequently isolated using column chromatography and identified by nuclear magnetic resonance. The characterized compound was also tested against chloroquine-resistant P. falciparum in culture to evaluate its antiplasmodial activity. The ethanol extract of S. wallichii at 100 µg/m1 exhibited a significant parasite shrinkage after 24 h of treatment. The ethyl acetate fraction at 100 µg/m1 was the most active frac¬tion against chloroquine-resistant P. falciparum. Based on the structural characterization, the major compound isolated from the ethyl acetate fraction was kaempferol-3-O-rhamnoside. which showed promising antiplasmodial activity against chloroquine-resistant P. falciparum with an IC50 of 106 µM after 24 h of treatment. The present study has provided a basis for the further investigation of kaempferol-3-O-rhamnoside as an active compound for potential antimalarial therapeutics.