STUDI FITOKIMIA IRVINGIA MALAYANA SEBAGAI ANTIMALARIA DARI HUTAN MERU BETIRI DALAM RANGKA DRUG DISCOVERY

Ayik R. Puspaningtyas
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Abstract

Meru Betiri forest in Jember contains a lot of medicinal plants. Irvingia malayana (Pauh Kijang), which is one of the medicinal plants found, has been proven as an antimalarial. However, phytochemical and antimalarial studies of Irvingia malayana have never been carried out. This study was conducted for an antimalarial Drug Discovery through phytochemical study by isolating the roots, stems, and leaves of Irvingia malayana. From the analysis using FTIR, H-NMR, and GC-MS, it was concluded that the compound in the ethyl acetate extract of Irvingia malayana stem was terpenoids that was included in silymarin group as well as other plants in the genus Irvingia. The melting point of Irvingia malayana isolate was 120-121oC with white crystals. Statistical result of in vivo study showed that each group was significantly different. On day 4 after administration, IC50 showed was 11,827 mg/kgBW and day 3 was 6,927 mg/kgBW. Therefore, 3 days is the maximum duration of administration in reducing plasmodium and shows the most excellent activity as antimalarial. In in vitro study, IC50 of Irvingia malayana (62.855 ug/ml) has weak activity of antiplasmodium compared to chloroquine positive controls containing IC50 (1,114x10-3 ug/ml). Based on the data of in vivo and in vitro antimalarial activities, the compound had no antimalarial activity because the extract consisted of many components that possessed many possible synergetic mechanisms of antimalarial if compared to single compound.Keywords: 
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十二月的Meru Betiri森林有很多药用植物。其中一种被发现的药用植物马来亚树(Pauh Kijang)已被证明是一种抗疟药。然而,从未进行过马来亚树的植物化学和抗疟疾研究。本研究通过分离马来树的根、茎、叶进行植物化学研究,以期发现抗疟药物。通过FTIR、H-NMR、GC-MS等分析,得出马来沙星茎乙酸乙酯提取物中的化合物为水飞蓟素类萜类化合物,与其他马来沙星属植物属化合物相同。马来亚Irvingia malayana分离物熔点为120-121℃,呈白色结晶。体内研究统计结果显示各组间差异有统计学意义。给药后第4天IC50为11,827 mg/kgBW,第3天IC50为6,927 mg/kgBW。因此,3天是减少疟原虫的最长给药时间,并显示出最优异的抗疟活性。在体外研究中,与含有IC50 (1,114 × 10-3 ug/ml)的氯喹阳性对照相比,马来亚苋的IC50 (62.855 ug/ml)具有较弱的抗疟原虫活性。根据体内和体外抗疟活性数据,该化合物不具有抗疟活性,因为该提取物由许多成分组成,与单一化合物相比,这些成分具有许多可能的协同抗疟机制。关键词:
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