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AKTIVITAS ANTIOKSIDAN DARI EKSTRAK ETANOL DAUN UNGU (Graptophyllum pictum L. Griff) Ni Luh Rustini; Ni Komang Ariati
CAKRA KIMIA (Indonesian E-Journal of Applied Chemistry) Vol 5 No 2 (2017)
Publisher : Magister Program of Applied Chemistry, Udayana University, Bali-INDONESIA

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (521.275 KB)

Abstract

ABSTRAK: Penelitian ini dilakukan untuk mengetahui kandungan total fenol, total flavonoid, dan aktivitas antioksidan berbagai fraksi dan ekstrak etanol daun ungu (Graptophyllum pictum L. Griff) secara in vitro. Penentuan total fenol menggunakan metode Manian dengan pereaksi Folin Ciocalteu dan total flavonoid dengan metode Aluminium Klorida. Penentuan aktivitas antioksidan menggunakan metode penangkapan radikal bebas 2,2-difenil-1-pikrilhidrazil (DPPH). Hasil ekstraksi 700 g serbuk kering daun ungu dengan 6000 mL etanol 96% menghasilkan 31 g ekstrak kental yang berwarna ungu kehijauan. Hasil partisi 15 g ekstrak kental etanol dengan pelarut kloroform, etik asetat dan n-butanol menghasilkan 12,5 g ekstrak pekat kloroform, 1,4 g ekstrak pekat etil asetat dan 1,0 g ekstrak pekat n-butanol yang semuanya berwarna ungu. Kandungan total fenol ekstrak etanol, kloroform, etil asetat dan n-butanol berturut-turut sebesar 3870,75 ; 2851,63 ; 7540,12 dan 18455,30 mg/100 g GAE. Kandungan total flavonoid ekstrak etanol, kloroform, etil asetat dan n-butanol berturut-turut sebesar 402,88 ; 98,14 ; 374,45 dan 345,95 mg/100 g QE. Hasil uji aktivitas antioksidan menunjukkan bahwa ekstrak etanol, etil asetat dan n-butanol daun ungu mempunyai kemampuan menangkap radikal bebas DPPH dengan nilai IC50 berturut-turut sebesar 83,25 ppm ; 271,04 ppm dan 385,82 ppm. Ekstrak kloroform daun ungu tidak memiliki kemampuan menangkap radikal bebas DPPH karena memiliki nilai IC50 lebih dari 500 ppm, yaitu sebesar 1365,73 ppm. ABSTRACT: This research has been done to determine the content of total phenol, total flavonoids and antioxidant activity in vitro of various fractions and ethanol extract of ungu leaves (Graptophyllum pictum L. Griff). Determination of total phenols using Manian method with Folin Ciocalteau reagent and total flavonoids using Aluminium chloride methode. Determination of antioxidant activity using DPPH method. The extraction of 700 g of dry powder ungu leaves with 6000 mL ethanol of 96 % produces 31 g of concentrated extract greenish purple. The partition of 15 g concentrated ethanol extract with chloroform, ethyl acetate and n-butanol to yield of 12.5 g concentrated chloroform extract, 1.4 g concentrated extract of ethyl acetate and 1.0 g of n-butanol concentrated extracts of which were purple. The content of total phenol of ethanol, chloroform, ethyl acetate and n-butanol extract in a row amounted to 3870.75; 2851.63; 7540.12 and 18455.30 mg/100 g GAE. The content of total flavonoid of ethanol, chloroform, ethyl acetate and n-butanol extract in a row amounted to 402.88; 98.14; 374.45 and 345.95 mg / 100 g QE. The result of antioxidant activity of ethanol, ethyl acetate and n-butanol extract of ungu leaf have the potent scavenger of free radicals DPPH with IC50 values were 83.25 ppm; 271.04 ppm and 385.82 ppm. Ungu leaf chloroform extract does not have potent scavenger of free radicals DPPH because it has IC50 values was 1365,73 ppm ??, more than 500 ppm,
UJI TOKSISITAS EKSTRAK DAUN WARU (Hibiscus tiliaceus L.) TERHADAP LARVA Artemia salina Leach SERTA IDENTIFIKASI GOLONGAN SENYAWANYA Ni Luh Rustini; Komang Ariati; A. A. Indah Purna Dewi; I Made Dira Swantara
Jurnal Kimia (Journal of Chemistry) Vol. 9, no. 1 Januari 2015
Publisher : Program Studi Kimia, FMIPA, Universitas Udayana (Program of Study in Chemistry, Faculty of Mathematics and Natural Sciences, Udayana University), Bali, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (100.25 KB) | DOI: 10.24843/JCHEM.2015.v09.i01.p08

Abstract

The “Brine Shrimp Lethality Test” (BSLT) is a preliminary test used to monitor the bioactive compounds from natural products as anti-cancer. This research aimed to determine of toxic compounds in the leaf of waru (Hibiscus tiliaceus L.). Maceration of 900 g waru leaf powder with 7000 mL of ethanol (5x24 hours) yielded 53,19 g ethanol extract with toxicity tests to larvae of Artemia salina Leach (LC50) of 79.43. The ethanol extract was partitioned to yield 1,81 g of n-hexane (LC50 = 63,09 ppm), 1,52 g of chloroform (LC50 = 1000 ppm) and 50,08 g of aqueous extract (LC50 = 316 ppm). The most toxic, n-hexane extract, was then separated , purified and identified. n-hexane extract was separated by column chromatography with silica gel 60 as stationary phase and n-hexane-chloroform-ethanol (5:4:1) as mobile phase to yield 7 fractions. Fraction one (F1) with a single stain on thin-layer chromatography was the most toxic (LC50 = 398 ppm). Identification with phytochemical test, UV-Vis spectrophotometer and IR spectrophotometer,  showed that the isolate contained sterol compounds.
SENYAWA STEROID PADA DAUN GAYAM (Inocarpus fagiferus Fosb) DAN AKTIVITASNYA SEBAGAI ANTIOKSIDAN TERHADAP DIFENILPIKRIL HIDRAZIL (DPPH) I Gusti Agung Putu Surya Adi Krisna; Sri Rahayu Santi; Ni Luh Rustini
Jurnal Kimia (Journal of Chemistry) Vol. 8, No. 2 Juli 2014
Publisher : Program Studi Kimia, FMIPA, Universitas Udayana (Program of Study in Chemistry, Faculty of Mathematics and Natural Sciences, Udayana University), Bali, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (124.611 KB) | DOI: 10.24843/JCHEM.2014.v08.i02.p17

Abstract

This research aimed to identify steroid compound from leaf of gayam (Inocarpus fagiferus Fosb) and test its antioxidant activity. Dried leaf powder of gayam was extracted with 5000 mL of 96% ethanol to yield 28,05 g concentrated extract. This extract was then fractionated into n-hexane and choloform to yield 14,18 g n-hexane and 2,21 g choloform fractions respectively. The test using Lieberman Burchard reagent showed that both fractions contain steroid, but n-hexane fraction contained more steroid than chloroform fraction. Separation of n-hexane fraction was done using silica gel column chromatography with n-hexane : ethanol (7:3) as eluent and four groups of fraction were obtained. Fraction F1 contained steroid and was relatively pure therefore it was then identified. The infrared and ultraviolet-visible spectra suggest that the isolate (F1 fraction) has functional groups such as O-H, C=O, C-H, and unconjugated C=C and showed lmax at 279,407, and 669 nm. The antioxidant test showed that the isolate had antioxidant activity toward DPPH with IC50 of 4 ppm.
ISOLASI DAN IDENTIFIKASI SENYAWA SITOTOKSIK DAUN NAGASARI (Calophyllum nagassarium Burm.f.) TERHADAP LARVA Artemia salina Leach I Wayan Pramana Eka Putra; Sri Rahayu Santi; Ni Luh Rustini
Jurnal Kimia (Journal of Chemistry) Vol. 10, No. 1 Januari 2016
Publisher : Program Studi Kimia, FMIPA, Universitas Udayana (Program of Study in Chemistry, Faculty of Mathematics and Natural Sciences, Udayana University), Bali, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (190.035 KB) | DOI: 10.24843/JCHEM.2016.v10.i01.p13

Abstract

Calophyllum nagassarium Burm.f. or nagasari is a kind of plant that often be used as medical plant such as for antiseptic, laxative, blood purifier, helminthic, and tonic. This study aimed to isolate and identify cytotoxic compounds of nagasari leaves by extracting 1000 g of leaf powder with 10 L of 96% ethanol  (5L x 2) to produce 66.81 g of ethanol extract (LC50 = 19.06 ppm). Fractionation of the ethanol-water extract (7: 3) in a row with 300 mL of n-hexane, chloroform 400 mL, 400 mL of n-butanol, and water and toxicity tests against larvae of Artemia salina Leach generate 2.52 g of n-hexane extracts (LC50 = 275.42 ppm), 7.06 g chloroform extract (LC50 = 63.10 ppm), 9.54 g of n-butanol extract (LC50 = 27.54 ppm) and 25.38 g aqueous extract (LC50 = 478 , 63 ppm). N-buthanol extract which was the most toxic was then separated, purified and identified. The separation of 2.0 g of n-butanol extract using column chromatography techniques with silica gel 60 as the stationary phase and chloroform- n-butanol (5: 3) as the mobile phase resulted in 5 fractions (F1, F2, F3, F4, and F5). Fraction F1 which was the most toxic (LC50 = 91.20 ppm) was then separated by preparative Thin Layer Chromatography and resulted two fractions (FA and FB). Fraction FB was the most toxic with LC50 = 83.18 ppm. UV-Vis and IR spectrophotometric analysis of FB identified a compound suspected to be terpenoides that has the characteristics of functional groups such as O-H, O = C-OH, aliphatic C-H.
PEMBERIAN EKSTRAK ETANOL BUAH BUNCIS (Phaseolus vulgaris L.) UNTUK MENURUNKAN KOLESTEROL TOTAL, Low Density Lipoprotein (LDL) DAN MENINGKATKAN High Density Lipoprotein (HDL) PADA TIKUS WISTAR DIET TINGGI LEMAK Sri Wahjuni; Ni Luh Rustini; Putu Yuliantari
Jurnal Kimia (Journal of Chemistry) Vol. 10, No. 1 Januari 2016
Publisher : Program Studi Kimia, FMIPA, Universitas Udayana (Program of Study in Chemistry, Faculty of Mathematics and Natural Sciences, Udayana University), Bali, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (77.755 KB) | DOI: 10.24843/JCHEM.2016.v10.i01.p14

Abstract

Excessive fat consumption can increase blood cholesterol level. Phytosterol composition in the plant can decrease blood cholesterol level. One of the plants that contain phytosterol is beans. This study was to prove the effect of antihypercholesterol the ethanol extract of the beans (Phaseolus vulgaris L.) with variety of doses of 50 mg/Kg BW; 100 mg/Kg BW and 150 mg/Kg BW in male Wistar rats with high fat level condition. Subjects of this study were 24 Wistar rats divided into 6 groups randomly with posttest control group study design. First group as negative control, second group as positive control, and the third (high cholesterol diet and ethanol extract in dose of 50 mg/kg,bw), fourth ( high cholesterol diet and ethanol extractin dose of 100 mg/kg,bw), fifth ( high cholesterol diet and ethanol extract in dose of 150 mg/kg,bw),  sixth (high cholesterol diet and simvastatin drug). The data was analyzed with ANOVA Tukey test. The result of this study shows total cholesterol levels decrease 23,88%; 30,14%; 35,82%. Cholesterol LDL levels decrease 38,09%; 52,38%; 61,35%. Cholesterol HDL levels increase 21,86%; 56,56%; 63,84%. Dose variant on this study giving the best result to decrease total cholesterol levels and LDL was 150 mg/Kg BW. Furthermore, 100 mg/Kg BW dose gave the best result to increase HDL cholesterol level. Based on the results it can be suggested that beans ethanol extract is able to decrease total cholesterol level, LDL and increase HDL cholesterol levels.  
PEMANFAATAN TEH KOMBUCHA SEBAGAI OBAT HIPERURISEMIA MELALUI PENURUNAN KADAR 8-HIDROKSI-2-DEOKSIGUANOSIN Made Baruna Jayadilaga; Ida Bagus Putra Manuaba; Ni Luh Rustini
Jurnal Kimia (Journal of Chemistry) Vol. 8, No. 1 Januari 2014
Publisher : Program Studi Kimia, FMIPA, Universitas Udayana (Program of Study in Chemistry, Faculty of Mathematics and Natural Sciences, Udayana University), Bali, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (281.826 KB) | DOI: 10.24843/JCHEM.2014.v08.i01.p17

Abstract

The utilization of kombucha tea as hyperuricemia medicine by decreasing levels of 8-hydroxy-2-deoksiguanosin (8-OHdG) has been carried out. This study aimed to determine the ability of kombucha tea to decrease uric acid and 8-OHdG levels in hyperuricemia rats. This research is true experimental with posttest only control group design. Rats that had experienced hyperuricemia were given kombucha tea dose of 10 mL/kg body weight and 40 mL/kg body weight of 4, 8, and 12 days fermentation period. The results showed that kombucha tea can decrease uric acid and 8-OHdG levels in hyperuricemia rats. The best dose of kombucha tea in decreasing uric acid and 8-OHdG levels was 40 mL/kg body weight with 8 days fermentation period. The decrease of uric acid and 8-OHdG levels were 93.88% and 85.89% respectively.
BILANGAN PEROKSIDA, BILANGAN ASAM, DAN KADAR FFA BIODIESEL DENGAN PENAMBAHAN ANTIOKSIDAN DARI KULIT BUAH PISANG KEPOK (Musa paradisiaca Linn.) Ni Made Sukma Sanjiwani; Ni Made Suaniti; Ni Luh Rustini
Jurnal Kimia (Journal of Chemistry) Vol. 9, No. 2 Juli 2015
Publisher : Program Studi Kimia, FMIPA, Universitas Udayana (Program of Study in Chemistry, Faculty of Mathematics and Natural Sciences, Udayana University), Bali, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (139.064 KB) | DOI: 10.24843/JCHEM.2015.v09.i02.p17

Abstract

The peel of banana kepok fruit (Musa paradisiaca Linn.) contains compound that function as an antioxidant in biodiesel. The purposes of this study were to determine the peroxide number, acid number, and FFA content of biodiesel from waste palm oil with addition of chloroform extract (EKKBPK). Biodiesel was synthesized using esterification reaction of wasted palm oil with methanol (10:1) and by transesterification reaction (4:1), the extract of peel of banana kepok fruit was theen added with various concentration of 0,1 % w/v (A1); 0,2 % w/v (A2); and 0,3 % w/v (A3) to the reaction mixtures. The peroxide number, acid number, and FFA content of synthesized biodiesel obtained in this research were 9.3591 meq peroxide/1000 g; 0.7221 mg KOH/g; and 0.33% repectively; biodiesel without addition of EKKBPK (12.2746 meq peroxide/1000 g; 0.6492 mg KOH/g; and 0.30%); and biodiesel with addition of EKKBPK 0.1 % w/v (11,1878 meq peroxide/1000 g; 0,4814 mg KOH/g; and 0.22%); 0.2 % w/v (9.7508 meq peroxide/1000 g; 0.3501 mg KOH/g; and 0.16%); and 0.3 % w/v (12.2512 meq peroxide/1000 g; 0.5217 mg KOH/g; and 0.24%). The acid numbers of those biodiesel were in acordance to the acid number of SNI 04-7182-2006. The addition of 0.2 % w/v EKKBPK on biodiesel showed the lowest peroxide number, acid number, and FFA content threfore it was the most effective in inhibiting the oxidation reaction of biodiesel.
AKTIVITAS ANTIJAMUR MINYAK ATSIRI RIMPANG DRINGO (Acorus calamus L.) TERHADAP JAMUR Botryodiplodia theobromae PENYEBAB BUSUK BUAH PISANG N. L. Rustini
Jurnal Kimia (Journal of Chemistry) Vol. 4, No. 2 Juli 2010
Publisher : Program Studi Kimia, FMIPA, Universitas Udayana (Program of Study in Chemistry, Faculty of Mathematics and Natural Sciences, Udayana University), Bali, Indonesia

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Abstract

A compound with antifungal activity has been isolated from dringo (Acorus calamus L.) essential oil. Steamdistillation was conducted to isolate the oil and resulted in 0.5 % yield. Antifungal activity test towardsBotryodiplodia theobromae showed that the ethanol posseses antifungal activity with an inhibition capacity of 94.4%. GC-MS analysis resulted in three main peaks at 15.008; 15.233; and 16.490 minutes. It was suggested from thepeak intensity that the last peak represents the major component of the extract. Futher more according to the librarydata base, the spectra of this compound matches with the Asarone spectra.
EFEK EKSTRAK ETANOL BIJI JAGUNG (ZEA MAYS) TERHADAP PROFIL LIPID TIKUS WISTAR DENGAN DIET TINGGI LEMAK Ni Luh Rustini; Komang Ariati; Wiwik Susanah Rita
Jurnal Kimia (Journal of Chemistry) Vol. 11. No.2 Juli 2017
Publisher : Program Studi Kimia, FMIPA, Universitas Udayana (Program of Study in Chemistry, Faculty of Mathematics and Natural Sciences, Udayana University), Bali, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (183.511 KB) | DOI: 10.24843/JCHEM.2017.v11.i02.p08

Abstract

Pada penelitian ini dipelajari efek ekstrak etanol biji jagung (Zea mays) terhadap profil lipid tikus wistar dengan diet tinggi lemak. Penelitian ini bertujuan untuk membuktikan efek antihiperkolesterolemia dari ekstrak etanol biji jagung dengan variasi dosis 50 mg/Kg BB; 100 mg/Kg BB dan 150 mg/Kg BB. Subjek penelitian ini ialah 24 ekor tikus Wistar yang dibagi menjadi 6 kelompok secara random dengan design penelitian posttest only control group design. Data hasil penelitian di analisis dengan uji tukey anova. Ekstrak etanol biji jagung dapat menurunkan kadar kolesterol total tikus wistar dengan diet tinggi lemak dengan dosis 50 mg/Kg BB, 100 mg/Kg BB dan 150 mg/Kg BB sebesar 5,44%; 12,89% dan 19,77%. Kadar kolesterol LDL dapat diturunkan dengan dosis 50 mg/Kg BB, 100 mg/Kg BB dan 150 mg/Kg BB sebesar 2,55%; 8,74% dan 15,66%. Kadar kolesterol HDL dapat ditingkatkan dengan dosis 50 mg/Kg BB, 100 mg/Kg BB dan 150 mg/Kg BB sebesar 1,5%; 2,08% dan 3,24%. Hasil uji fitokimia menunjukkan bahwa ekstrak etanol biji jagung positif mengandung senyawa golongan steroid dan fenol. Senyawa tersebut memiliki aktivitas antioksidan dan dapat meningkatkan antioksidan endogen di dalam tubuh, sehingga dapat menurunkan kolesterol darah.
SKRINING ANTIKANKER MELALUI PENDEKATAN UJI TOKSISITAS TERHADAP LARVA UDANG (Artemia salina Leach) SERTA IDENTIFIKASI GOLONGAN SENYAWA AKTIF PADA BUAH PLUM (Prunus domestica L.) Ni Made Susita Pratiwi; I Made Dira Swantara; Ni Luh Rustini
Jurnal Kimia (Journal of Chemistry) Vol. 9, no. 1 Januari 2015
Publisher : Program Studi Kimia, FMIPA, Universitas Udayana (Program of Study in Chemistry, Faculty of Mathematics and Natural Sciences, Udayana University), Bali, Indonesia

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (126.382 KB) | DOI: 10.24843/JCHEM.2015.v09.i01.p12

Abstract

Isolation and identification of toxic compounds from ethanol extract of Prunus domestica L. have been conducted. Extraction of 1000 gr of plum fruit produced 128,75 g concentrated ethanol extract. The results of toxitcity tests of the extract using Artemia salina L. larvae showed the LC50 value of 100 ppm. Partition of ethanol extract yielded chloroform (10,52 g), n-hexane (26,58 g), and water (52,57 g) extracts. The toxicity test showed the chloroform extract to be the most toxic with LC50 of 31,97 ppm. Chloroform extract was separated by column chromatography using silica gel as stationary phase and chloroform : ethanol : water (5:4:1) as mobile phase giving three fractions. The toxicity test showed that fraction II was the most toxic with LC50 of 364,74 ppm. The phytochemical test result showed  that fraction II (the active isolate) belonged to terpene groups. Analysis using UV-Vis spectrophotometer showed three peaks at 241,  409, and 668 nm, showing the possibility of the presence of funtional groups of C-H aliphatic, C-O alkoholic and C=O, respectively