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INDONESIA
Majalah Obat Tradisional
ISSN : 14105918     EISSN : 24069086     DOI : -
Core Subject : Health,
raditional Medicine Journal (Majalah Obat Tradisional), or Trad. Med. J. (ISSN 1410-5918 (print) and ISSN 2406-9086 (online)), is an international scientific journal published by Faculty of Pharmacy, Universitas Gadjah Mada, three times annually. Collaborating with Indonesian Pharmacist Association, Daerah Istimewa Yogyakarta, and we dedicate our journal to researches and development in traditional medicine. The journal receives papers on research laboratory, field research, and case studies of traditional medicine and its constituent, covering research topics including raw materials, cultivation, phytochemical, pharmacological effects and toxicology, formulation, and biotechnology.
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Articles 18 Documents
Search results for , issue "Vol 16, No 3 (2011)" : 18 Documents clear
AKTIVITAS ANTIDIABETES KOMBINASI EKSTRAK TERPURIFIKASI HERBA SAMBILOTO (Andrographis paniculata (Burn.F.) NESS.) DAN METFORMIN PADA TIKUS DM TIPE 2 RESISTEN INSULIN Eka Siswanto Syamsul; Agung Endro Nugroho; Suwijiyo Pramono
Majalah Obat Tradisional Vol 16, No 3 (2011)
Publisher : Faculty of Pharmacy, Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (682.952 KB) | DOI: 10.22146/tradmedj.8049

Abstract

A. paniculata is a plant that can be used to overcome the disease diabetes. In DM there is a possibility of the use of therapy with oral hypoglycemic drugs, for example: metformin. This research was conducted using a complete random method indirectional pattern. This study aims to determine the potential of the combination of purified extract of sambiloto herbs and enhancement effects of metformin on blood glucose levels decrease in insulin resistant rats. Test animals used were divided 4 groups, group 1: metformin 45 mg / kg (positive control), group 2: purified extract of sambiloto herbs 434.6 mg/ kg, group 3: a combination of metformin 45 mg / kg BW with the extract of 434.6 mg/ kg (combination 1), and group 4: metformin 22.5 mg/ kg body weight with extract 434.6 mg/ kg (combination 2). Test animals are insulin resistant type 2 DM was made by administering 1.8 g fructose / kg body weight and fat diet for 50 days. Assay of glucose using a reagent kit. Observation of GLUT-4 expression in muscle cells by using immunohistochemical techniques. Insulin resistance rats was tested by using three parameters: (1) testing of blood glucose levels preprandial and postprandial (2) the hypoglycaemic activity of glibenclamide, and (3) observations of GLUT-4 protein expression in muscle tissue. Test results show that the animals had insulin resistant. Results, in this research antidiabetic activity assay indicate that the hypoglycaemic for combination 1 and combination 2 lower compared to a single administration of metformin or purified extract (p<0,05). From the above results concluded that the combination of sambiloto extract purified with metformin does not increase the potency of antidiabetic in single use.
IDENTIFIKASI SENYAWA ANTIFUNGI DARI KULIT BATANG KECAPI (Sandoricum koetjape) DAN AKTIVITASNYA TERHADAP Candida albicans Warsinah Warsinah; Eka Kusumawati; Sunarto Sunarto
Majalah Obat Tradisional Vol 16, No 3 (2011)
Publisher : Faculty of Pharmacy, Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (933.563 KB) | DOI: 10.22146/tradmedj.8055

Abstract

Kecapi (Sandoricum koetjape (Burm.f.) Merr) was one of the traditional medicine from  family Meliaceae and had compounds such as flavonoids, saponins and polyphenols that can be used as antifungal. The objective of this research to know compounds contained from S. koetjape bark that has potential as an antifungal toward C. albicans.Research carried out two stages using  extraction by maceration with methanol and fractionation by column chromatography method used the solvent n-hexane, chloroform, ethyl acetate and methanol. The next step was examined its activity toward C. albicans and identification of fraction active compounds with the Gas Chromatograpy-Mass Spectrometry (GC-MS). The results of this research showed that methanol extract from S. koetjape bark had antifungal activity againstC. albicans (39,654%). Next, the methanol extract was fractionated and fractionation results were obtained six fractions with the greatest antifungal activity of fraction III, followed by fraction V (39.66% b/v), fraction IV (39.02% b/v), fraction II (37.91% b/v), fraction VI (35.48 % b/v) and fraction I (33.72% b/v). Identification of compounds with GC-MS in fraction III and compounds contained have potential as an antifungal are α-gurjunene, trans-caryophyllene, aromadendrene, α-humulene, β-caryophyllene, δ-Cadinene, alloaromadendrene, octadecanoic acid (as. stearat), hexadecanoic acid metil ester (metil palmitate), hexadecanoic acid (as. palmitate), 9-octadecenoic acid metil ester (metil elaidate), 9-octadecenoic acid (as. oleat).
ANALISIS FLAVONOID DAN TANNIN DENGAN METODA MIKROSKOPI-MIKROKIMIAWI Sri Mulyani; Toga Laksana
Majalah Obat Tradisional Vol 16, No 3 (2011)
Publisher : Faculty of Pharmacy, Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (828.417 KB) | DOI: 10.22146/tradmedj.8047

Abstract

Studies have been conducted to analyze flavonoids and tannins using microscopy-microchemical methods. Materials used for the analysis of flavonoid were orange peel, sonchi leaves, and orthosiphon leaves, with N. exaltata as negative control. While guajava leaves, guazama leaves, and areca seed were used for the analysis of tannins, with ginger rhizome as negative control. The study was conducted in a way of material sliced crosswise, subsequently given the identification reagent for flavonoids (ammonia, NaOH, AlCl3, sitroborat). On the other hand, using FeCl3, fast blue salt, and prusian blue for tannins. Having examined under a microscope, the area which gave a positive reaction to the reagent used, indicate the test materials contained compounds that were analyze. The results showed that this microscopy-microchemical method can be used to analyze the presence of flavonoids / tannins in the test material. Presence of flavonoid compounds will give yellow color with ammonia, NaOH, AlCl3, sitroborat reagent, while blue to black for the tannins with FeCl3, red with fast blue salt, and blue with prusian blue.
ANALISIS AKTIVITAS ANTIOKSIDAN DAN KANDUNGAN ANTOSIANIN TOTAL EKSTRAK DAN LIPOSOM KELOPAK BUNGA ROSELLA (Hibiscus Sabdariffa L.) I Gede Agus Juniarka; Endang Lukitaningsih; Sri Noegrohati
Majalah Obat Tradisional Vol 16, No 3 (2011)
Publisher : Faculty of Pharmacy, Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (706.251 KB) | DOI: 10.22146/tradmedj.8048

Abstract

The form of liposome formulations is one of strategies to overcome the limitations of anthocyanin extract stability of roselle calyx (Hibiscus sabdariffa L.). In this study, antioxidant comparative analysis of antioxidant activity and total anthocyanin content from rosella extract and its liposomes form was conducted. Preparation of extract made by maceration using the best solvent consisted of methanol : formic acid (97:3) (v/v). From this procedure, the obtained extract was about 26.40% and antioxidant activity was 19.99%. Liposome formulations of methanol extract from roselle calyx were prepared by reverse phase method using rosella extract as aqueous phase and egg lecithin as the lipid phase. The stability of exctract and liposome form of rosella calyx was compared. The stability study showed that there was a reduction of antioxidant activity (DPPH test) 11.25 % for the roselle extract, while the liposome form was 0.93% after 30 days storage in low temperature (0-50C) and saturated nitrogen. In addition, total anthocyanin content (pH differential method test) decreased approximately 39.12 % for  the roselle extract and 0.72% for the liposome form. More over, the liposome had lower level of irritation than the form of extract. Therefore, it can be concluded that anthocyanin encapsulated by liposome was more stable, safe, and effective than the anthocyanin of the rosella calyx extract.
AKTIVITAS PENANGKAPAN RADIKAL 2,2-DIFENIL-1-PIKRILHIDRAZIL OLEH EKSTRAK ETANOLIK BATANG BROTOWALI (Tinospora crispa (L.) Miers) DAN FRAKSI-FRAKSINYA Tatang Irianti; Andayana Puspitasari; Ema Suryani
Majalah Obat Tradisional Vol 16, No 3 (2011)
Publisher : Faculty of Pharmacy, Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (760.318 KB) | DOI: 10.22146/tradmedj.8051

Abstract

We have investigated the antiradical activity of ethanolic extracts of Brotowali stem (Tinospora crispa (L.) Miers) using radical scavenging assay or DPPH radical. Thin layer chromatograms were also studied to estimate the group of compounds that have antiradical activity. The ethanolic extract, ethyl acetate and water fractions were showed coumarin and flavonoid. The DPPH antiradical efficiency values of ethyl acetate fraction was the highest antiradical activity namely 200 µg/ mL of this fraction was able to inhibit 53.57% DPPH radicals. 
AKTIVITAS PENANGKAP RADIKAL BEBAS DARI BATANG PAKIS (Alsophila glauca J. Sm) Sri Wahdaningsih; Erna Prawita Setyowati; Subagus Wahyuono
Majalah Obat Tradisional Vol 16, No 3 (2011)
Publisher : Faculty of Pharmacy, Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (603.305 KB) | DOI: 10.22146/tradmedj.8053

Abstract

Free radical induced oxidative stress that influences the occurrence of various degenerative diseases such as cancer, coronary heart disease and premature aging. In the case that body's antioxidant defense system does not have excessive antioxidants, additional natural antioxidant via food or other nutrients intake is needed. Stems of ferns are known to contain phenolic compounds that are known to have antioxidant activity. A study has been carried out to determine antioxidant potential of stems of ferns of western Borneo origin compared to quercetin as positive control. Initially, material was macerated gradually with wasbenzen followed by methanol. The extract obtained was filtered and evaporated to dryness to give dried wasbenzen extract and methanol extract respectively. Antioxidant properties of extracts were performed by DPPH on TLC. Active (wasbenzen) extract was then partitioned with 80% methanol to give soluble and insoluble fractions. Active (insoluble) fraction was further fractionated by vacuum liquid chromatography using a gradient mobile phase with increasing polarity (wasbezen: chloroform). Fractions obtained were tested antioxidant activity, and isolation was done by preparative TLC. The purity of isolated antioxidant compound was confirmed by TLC, and antioxidant potential was measured spectroscopically with DPPH method. This compound displayed antioxidant activity, but its value was lower than that of quercetin used as a positive control (IC50 178.4 v / s 2.17 microg / mL)
DAYA ANTIMIKROBA METABOLIT BIOAKTIF JAMUR SHIITAKE (Lentinula edodes (Berk.) Pegler) YANG DIKULTUR PADA TIGA JENIS MEDIUM FERMENTASI Nuraeni Ekowati; Rina Sri Kasiamdari; Nursamsi Pusposendjojo; C.J. Soegihardjo
Majalah Obat Tradisional Vol 16, No 3 (2011)
Publisher : Faculty of Pharmacy, Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (527.742 KB) | DOI: 10.22146/tradmedj.8050

Abstract

Shiitake mushroom (Lentinula edodes (Berk.) Pegler) is one of the fungi that has potentially been used as food and medicinal mushroom. Cultivation in liquid medium by the fermentation process has been developed over recent years. Four isolates of L.edodes (isolates from Malang, Cianjur, Lembang and Yogyakarta) cultured on three types of fermentation media (KM: Medium Kauffman; GYMT: Glucose, Yeast Extract, Malt Extract, Thiamin; YEMR: Yeast extract, Malt Extract, Rice bran). Bioactive metabolites  extracted from mycelium biomass and fermentation culture filtrates were tested using pathogenic microbial Staphylococcus aureus ATCC 25923, Escherichia coli ATCC 35218, Candida albicans ATCC 10231, and Trichophyton mentagrophytes. Inhibition zone diameter data were analyzed using analysis of variance followed by Duncan test at 5% error rate. The results showed that bioactive compounds in the culture filtrates and mycelium biomass of L. edodes extracted using chloroform, ethyl acetate and water, were able to inhibit S. aureus, E. coli and C. albicans,  but were not able to inhibit T.mentagrophytes. Isolates of L.edodes from Lembang and Yogyakarta cultured on Kauffman Medium gave  the best results with inhibitory zones of 24.97 to 31.14 mm. Microbes which gave the most sensitive of bioactive compounds test from L. edodes were C. albicans followed by E. coli, S. aureus and T. mentagrophytes. Bioactive metabolites from L. edodes inhibited potentially pathogenic microbes  from the group of  bacteria and  yeasts but did not inhibit the fungus.
ISOLASI DAN IDENTIFIKASI SENYAWA ANTIOKSIDAN DAUN KESEMEK (Diospyros kaki Thunb.) DENGAN METODEDPPH (2,2-DIFENIL-1-PIKRILHIDRAZIL) Isnindar Isnindar; Subagus Wahyuono; Erna Prawita Setyowati
Majalah Obat Tradisional Vol 16, No 3 (2011)
Publisher : Faculty of Pharmacy, Universitas Gadjah Mada

Show Abstract | Download Original | Original Source | Check in Google Scholar | Full PDF (776.457 KB) | DOI: 10.22146/tradmedj.8054

Abstract

Antioxidant is a substance which in small concentrations can significantly inhibit or prevent the oxidation of the substrate. One plant is efficacious as an antioxidant is the persimmon (Diospyros kakiThunb.) where is cultivated widely in East Asia, Spain and Indonesia. In the search for natural antioxidant compounds, have been studied isolation and identification of antioxidant compound of persimmon leaves (DiospyroskakiThunb.) using DPPH (2,2-diphenyl-1-pikrilhidrazil) method. The extraction of persimmon leaves was carried out by maceration method with wasbenzen. Extracts obtained by evaporating the solvent wasbenzenon a rotary evaporator and were then re-macerated with methanol. Antioxidant activity of extracts was evaluated with DPPH 0.2% method. Active extract was partitioned with chloroform, methanol, distilled water and tested for antioxidant activity by DPPH 0.2% method. The active compound was purified byPTLC and the purified active isolates was then confirmed by TLC. The antioxidant activity (IC50) active isolates were analyzed using spectrophotometry. Analysisof active isolates resulted the antioxidant activity (IC50) of 100.00 ug / ml. UV-Vis spectrum of the active isolates showed absorption at λmax 285 and 401 nm. Infrared spectra (KBR) showed absorption at 3446 cm-1 (OH), 2926 cm-1 (CHaliphatic), 1456 cm-1 (CH2), 1384 cm-1 (CH3), 1255 cm-1, and 1115 cm-1 (C-0-C), 1631 cm-1 (C=Caromatic). GC-MS spectra gave two peaks with retention time 11.408 minutes with a similarity index of 79.243% with the molecular ion (M•)+ appeared at m/z 178, 163, 147. These spectra are expected to be methyl eugenol. Furthermore, the peak with retention time 12.982 minutes with a similarity index of 20.757%, producing a mass spectrum with molecular ion peaks (M•)+appeared at m/z 192, 177, 161. These spectra are expected to be myristicin compound.

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