Nuzul Asmilia, T. Tr, D. Aliza, J. Melia, E. Rahmi, Lingga Surya Maret Daulay
{"title":"THE EFFECT OF MALACCA LEAVES (Phyllantus emblica) ETHANOLIC EXTRACT ON Plasmodium falciparum GROWTH IN VITRO","authors":"Nuzul Asmilia, T. Tr, D. Aliza, J. Melia, E. Rahmi, Lingga Surya Maret Daulay","doi":"10.21157/J.KED.HEWAN.V12I4.10215","DOIUrl":null,"url":null,"abstract":"The aim of this research was to find out in vitro antiplasmodium activity of Malacca leaves (Phyllantus emblica) ethanolic extract against Plasmodium falciparum growth. In this study, Plasmodium culture contained 5% parasitemia in ring stage was cultured using candle jar method and antiplasmodial activity test was carried out using microculture. The treatments were divided into 7 groups with four repetitions. K1 as negative control group was given Roswell Park Memorial Institute (RPMI), while K2 as positive control group was given artesdiaquine. Groups K3, K4, K5, K6, and K7 group was added with 100 µg/mL, 75 µg/mL, 50 µg/mL, 25 µg/mL, and 5 µg/mL of Malacca leaves ethanolic extract, respectively. Antiplasmodial activity was determined by inhibition concentration of 50% parasite growth (IC50). The data were analyzed using ANOVA and followed by Duncan test. The average of parasitemia level in group K1, K2, K3, K4, K5, K6, and K7 were 55.25±15.62, 8.50±2.52, 8.50±3.00, 9.25±0.95, 9.00±2.70, 9.79±2.06, and 10.75±2.22, respectively. The average of inhibition percentage in group K1, K2; K3; K4; K5; K6; and K7 were 0.00±0.00%, 84.62±4.55%; 84.62±5.43%; 83.26±1.73%; 83.71±4,90%; 82.35±3,73%; and 80.54±6.83%, respectively (P0.01). The results showed that the administration of malacca leaves ethanolic extract significantly affect (P0.01) the inhibition of Plasmodium growth as compared to group K1 (negative control). Probit analysis reveals the IC50 value was 3.889 µg/mL. In conclusion, all doses of malacca leaves ethanolic extract used in this study was able to inhibit Plasmodium falciparum growth with IC50 value was 3.889 µg/mL.","PeriodicalId":114727,"journal":{"name":"Jurnal Kedokteran Hewan - Indonesian Journal of Veterinary Sciences","volume":"66 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-12-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Jurnal Kedokteran Hewan - Indonesian Journal of Veterinary Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21157/J.KED.HEWAN.V12I4.10215","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
Abstract
The aim of this research was to find out in vitro antiplasmodium activity of Malacca leaves (Phyllantus emblica) ethanolic extract against Plasmodium falciparum growth. In this study, Plasmodium culture contained 5% parasitemia in ring stage was cultured using candle jar method and antiplasmodial activity test was carried out using microculture. The treatments were divided into 7 groups with four repetitions. K1 as negative control group was given Roswell Park Memorial Institute (RPMI), while K2 as positive control group was given artesdiaquine. Groups K3, K4, K5, K6, and K7 group was added with 100 µg/mL, 75 µg/mL, 50 µg/mL, 25 µg/mL, and 5 µg/mL of Malacca leaves ethanolic extract, respectively. Antiplasmodial activity was determined by inhibition concentration of 50% parasite growth (IC50). The data were analyzed using ANOVA and followed by Duncan test. The average of parasitemia level in group K1, K2, K3, K4, K5, K6, and K7 were 55.25±15.62, 8.50±2.52, 8.50±3.00, 9.25±0.95, 9.00±2.70, 9.79±2.06, and 10.75±2.22, respectively. The average of inhibition percentage in group K1, K2; K3; K4; K5; K6; and K7 were 0.00±0.00%, 84.62±4.55%; 84.62±5.43%; 83.26±1.73%; 83.71±4,90%; 82.35±3,73%; and 80.54±6.83%, respectively (P0.01). The results showed that the administration of malacca leaves ethanolic extract significantly affect (P0.01) the inhibition of Plasmodium growth as compared to group K1 (negative control). Probit analysis reveals the IC50 value was 3.889 µg/mL. In conclusion, all doses of malacca leaves ethanolic extract used in this study was able to inhibit Plasmodium falciparum growth with IC50 value was 3.889 µg/mL.
研究马六甲叶乙醇提取物对恶性疟原虫生长的体外抗疟原虫活性。本研究采用蜡烛罐法培养含5%环期寄生虫的疟原虫,并采用微培养法进行抗疟原虫活性试验。治疗分为7组,每组4次重复。K1阴性对照组给予罗斯威尔公园纪念研究所(Roswell Park Memorial Institute, RPMI)治疗,K2阳性对照组给予青蒿素。K3、K4、K5、K6、K7组分别添加马六甲叶乙醇提取物100µg/mL、75µg/mL、50µg/mL、25µg/mL、5µg/mL。采用50%抑制浓度(IC50)测定抗疟原虫活性。采用方差分析和Duncan检验对数据进行分析。K1、K2、K3、K4、K5、K6、K7组平均寄生水平分别为55.25±15.62、8.50±2.52、8.50±3.00、9.25±0.95、9.00±2.70、9.79±2.06、10.75±2.22。K1、K2组的平均抑制率;K3;K4;K5;转K6;K7分别为0.00±0.00%、84.62±4.55%;84.62±5.43%;83.26±1.73%;83.71±4 90%;82.35±3,73%;分别为80.54±6.83% (P0.01)。结果表明,与K1组(阴性对照)相比,马六甲叶乙醇提取物对疟原虫生长的抑制作用极显著(P0.01)。Probit分析显示IC50值为3.889µg/mL。综上所述,本研究使用的马六甲叶乙醇提取物均能抑制恶性疟原虫生长,IC50值为3.889µg/mL。