scholarly journals KAJIAN FRAKSI METANOL DARI EKSTRAK METILEN DIKLORIDA KULIT KAYU BATANG PELAWAN (Tristania whitiana Griff.) SEBAGAI ANTIBAKTERI

Molekul ◽  
2007 ◽  
Vol 2 (1) ◽  
pp. 1
Author(s):  
Purwantiningsih Sugita
Keyword(s):  
Antibacterial Activity ◽  
Minimum Inhibitory Concentration ◽  
Thin Layer ◽  
Thin Layer Chromatography ◽  
Inhibitory Concentration ◽  
Methanol Fraction ◽  
The Third ◽  
The One ◽  
Layer Chromatography ◽  
Chloroform Methanol

Antibacterial compound from methanol fraction of methylene dichloride extract of pelawan bark had been studied. Pelawan bark was extracted using ethanol 95% and CH2Cl2-water (1:1), respectively. Extract of CH2Cl2 was partitioned using hexane-methanol 90% (1:1). Afterwards, methanol fraction was analyzed by thin layer chromatography methods to find the best eluent for column chromatography. The best eluent came from mixture of acetone-chloroform-methanol (0,6:4:0,4). The fractionation yielded 16 fractions with the first (M1) and the third (M5) fractions became the one spotted fractions. M1 and M5 fractions were examined for their antibacterial activity using paper diffusion methods by determining minimum inhibitory concentration value. M1 fraction showed greater activity than M5 fraction with minimum inhibitory concentration value of 2,7857 mg/mL. The result of phytochemistry test showed that both fractions contain terpenoid.

scholarly journals Profile of Thin-Layer Chromatography and UV-Vis Spectrophotometry of Akar Kuning Stem Extract (Arcangelisia flava)

2018 ◽  
Vol 1 (2) ◽  
pp. 72-76 ◽  
Author(s):  
Mohammad Rizki Fadhil Pratama ◽  
Suratno Suratno ◽  
Evi Mulyani
Keyword(s):  
Thin Layer ◽  
Thin Layer Chromatography ◽  
Ethanol Extract ◽  
Retention Factor ◽  
Polar Solvents ◽  
Central Kalimantan ◽  
Stem Extract ◽  
Rf Values ◽  
Layer Chromatography ◽  
Chloroform Methanol

This study aims to obtain the profile of Thin-Layer Chromatography (TLC) and Ultraviolet-Visible (UV-Vis) spectrophotometry from ethanol extract of akar kuning stems (Arcangelisia flava) from Central Kalimantan. The TLC method is used with the orientation phase of the combination of polar-non-polar solvents resulting from orientation, while ethanol is used as the solvent for UV-Vis spectrophotometers. TLC results showed the formation of 3 stains on a combination of polar solvents chloroform : methanol : water while in a non-polar solvent combination n-hexane : ethyl acetate did not show any stains. Comparison of retention factor (Rf) values show the best combination of polar solvents to separate stains at a ratio of 5 : 2 : 1, respectively. Separation in 2-dimensional TLC with polar solvents showed a similar pattern with 1-dimensional separation in the form of 3 stains. UV-Vis spectrophotometer results showed 4 main peaks with wavelength 227.2; 267.4; 345.2; and 425.3 nm, respectively. The profile of the peak formed is very similar to that shown by berberine, one of the main metabolites of akar kuning. TLC and UV-Vis spectrophotometers profiles obtained are expected to support further research using akar kuning stems, especially those from Central Kalimantan.

scholarly journals ANTIOXIDANT AND ANTIBACTERIAL ACTIVITIES OF BIXIN PIGMENT FROM ANNATTO (Bixa orellana L.) SEEDS

2010 ◽  
Vol 7 (1) ◽  
pp. 88-92 ◽  
Author(s):  
Pipin T. Kurniawati ◽  
H. Soetjipto ◽  
Leenawati Limantara
Keyword(s):  
Antioxidant Activity ◽  
Antibacterial Activity ◽  
Thin Layer ◽  
Thin Layer Chromatography ◽  
Antibacterial Activities ◽  
Diffusion Method ◽  
Bixa Orellana ◽  
Isolation And Identification ◽  
Double Beam ◽  
Layer Chromatography

Research on Bixa orellana L. have been done to isolate, identify and determine bixin percentage, the antioxidant and antibacterial activities of bixin from B. orellana seed.  Isolation and identification of bixin was done by thin layer chromatography (TLC), column chromatography, chemical test of bixin and UV-Vis double beam spectroscopy. Percentage of bixin was calculated by JECFA method, the antioxidant activity was determined by DPPH (1-1 diphynilpicrylhidrazil) method while antibacterial activity was analyzed by the use of agar diffusion method. Thin layer chromatography (TLC) for the crude extract contained 5 spot, where spot 5th was bixin. Bixa orellana has 75±3% of bixin. Antioxidant activity of bixin had IC50 548.5±20.0 ppm. Whereas the antibacterial activity of bixin against the Escherichia coli and Staphylococus aureus could be classified as weak inhibition category at 500-750 μg and medium inhibition category at 1500 μg.   Keywords: Bixa orellana L., bixin, antioxidant, antibacteria

scholarly journals Physicochemical and antimicrobial assessment of Iranian Propolis gathered in Qazvin province

2020 ◽  
Vol 10 (2) ◽  
pp. 82
Author(s):  
Fatemeh Samieerad ◽  
Nematollah Gheibi
Keyword(s):  
Staphylococcus Aureus ◽  
Pseudomonas Aeruginosa ◽  
Minimum Inhibitory Concentration ◽  
Thin Layer ◽  
Inhibitory Concentration ◽  
Minimum Bactericidal Concentration ◽  
Antibacterial Effect ◽  
Ethanol Extract ◽  
Standard Strain ◽  
Layer Chromatography

Background: Propolis is one of the useful bee colony products that have been used in traditional medicine for centuries. In this study, the physicochemical characters and their antibacterial effect of Iranian Propolis collected from Qazvin province was assessed.Methods: In this study, Thin Layer Chromatography and Vacuum Liquid Chromatography to detect different compounds of the extract have been used. In the initial evaluation of Propolis extract, it was found that the extract includes variable compounds with different polarity; so, the initial classification of extract with different polarity solvents was essential. Finally, 0.1 gr hydro alcoholic Propolis was injected to the HPLC by ultrasound. The antibacterial effect of Iranian ethanol extract Propolis was measured using a microdilution method against Pseudomonas aeruginosa: P. aeruginosa and Staphylococcus aureus: S.aureus standard strains and the minimum bactericidal and inhibitory concentration were defined.Results: Primary analysis of the ethanol extract by analytical Thin Layer Chromatography, demonstrated the presence of flavonoid and phenol in it. Minimum inhibitory concentration and Minimum Bactericidal Concentration for Staphylococcus aureus: S.aureus standard strain was 2.5mg/ml. The same procedure was done for Pseudomonas aeruginosa: P. aeruginosa standard strain and the Minimum inhibitory concentration and Minimum Bactericidal Concentration were 50mg/ml of Propolis extracts.  Conclusion: According to the results, the alcoholic extract of propolis from Qazvin province of Iran provides significant antimicrobial activity. Its powerful activity may be due to high total phenolic and flavonoid contents.Keywords: Iranian propolis, Antibacterial activity, Phenolic compounds, Flavonoid compound

Standardization of Homoeopathic Mother Tincture of Strychnous nux vomica with the help of High-Performance Thin Layer Chromatography and correlation of its alkaloid markers with its Toxicological action

2021 ◽  
pp. 4203-4206
Author(s):  
Dharmendra B. Sharma ◽  
Parth Aphale ◽  
Vineet Sinnarkar ◽  
Sohan S. Chitlange ◽  
Asha Thomas
Keyword(s):  
Fatty Acids ◽  
Thin Layer ◽  
Thin Layer Chromatography ◽  
High Performance ◽  
Therapeutic Action ◽  
Aluminium Sheets ◽  
Mother Tincture ◽  
Layer Chromatography ◽  
Chloroform Methanol ◽  
Dark Blue

Background: Chromatography is one of the important laboratory technique in which the components of a mixture are separated on an adsorbent in order to analyze, identify, purify and quantify a mixture. Thin Layer Chromatography (TLC)is used to support the identity of a compound in a mixture when the Rf of a compound is compared with the Rf of a known compound. High Performance Thin Layer Chromatography is a sophisticated and automated form of Thin Layer Chromatography (TLC). The procedure simultaneously processes the sample and standard that results in better analytical precision and accuracy at a faster pace. Pharmacological/ Toxicological action of Nux Vomica is because of its active principles present in the seeds namely strychnine, brucine etc. This research paper aims to corelate the active principles present in Nux Vomica with the toxicological action of the same. Materials and Methods: 1. Standard Nux Vomica mother tincture was tested for its alkaloid markers and its correlation with the toxicological action was studied. 2. Analysis of the mother tincture was done using High Performance Thin Layer Chromatography. 3. Stationary phase consisted of TLC Aluminium sheets with silica gel 60 F253 pre-coated layer (20cm x 10cm), thickness-0.2mm, no. of tracks-18, band length-6mm. 4. Mobile Phase consisted of Chloroform: Methanol (9.5:0.5). 5. The plate was developed in developing chamber and observed under U.V. Light. Results: Colours seen on the HPTLC Plates of samples are greenwhich corresponds to strychnine, dark blue which corresponds to brucine, orange to alkaloids fluorescent green to sterols and pink to fatty acids which are evident on the chromatogram. Conclusion: Therapeutic action of Nux Vomica as noted in Homoeopathic Materia Medica is because of the active principles like strychnine, brucine, alkaloids, sterols, fatty acids present in it which is evident from the chromatogram.

EXPERIMENTAL PRODUCTION OF AFLATOXIN ON BRICK CHEESE1

1972 ◽  
Vol 35 (10) ◽  
pp. 585-587 ◽  
Author(s):  
C. N. Shih ◽  
E. H. Marth
Keyword(s):  
Thin Layer ◽  
Thin Layer Chromatography ◽  
Aspergillus Flavus ◽  
Aspergillus Parasiticus ◽  
Solvent System ◽  
Experimental Production ◽  
Mold Growth ◽  
Layer Chromatography ◽  
Plastic Containers ◽  
Chloroform Methanol

Brick cheese was placed in plastic containers and all surfaces except the top were sealed with wax. The top was inoculated with Aspergillus flavus or Aspergillus parasiticus and cheese was incubated in a humid chamber at 7.2, 12.8, and 23.9 C for up to 14 weeks after mold growth was evident. After incubation each cheese was cut horizontally into four layers, each approximately 1 cm thick. Each layer of cheese was extracted with a monophasic-biphasic solvent system (chloroform, methanol, and water). The extract was purified, concentrated, and aflatoxins were measured by thin-layer chromatography and fluorometry. No aflatoxins were produced by either mold at 7.2 C. At 12.8 C, A. parastticus developed aflatoxins B1 and G1 after 1 week of incubation. Aflatoxin produced by this mold persisted through 4 weeks of storage and then was not detectable. Aspergillus flavus did not form aflatoxin at 12.8 C. Both molds produced aflatoxin on cheese at 23.9 C; A. parasiticus did so after 1 week and A. flavus after 14 weeks. In some instances, aflatoxin was found in cheese 4 cm from the surface. It is reasonable to assume that cheese will not become contaminated with aflatoxin if the food is held at or below 7 C.

Toxicity tests in eight species of Chrysochromulina (Haptophyta)

1997 ◽  
Vol 75 (1) ◽  
pp. 129-136 ◽  
Author(s):  
Susanne Simonsen ◽  
Øjvind Moestrup
Keyword(s):  
Thin Layer ◽  
Thin Layer Chromatography ◽  
Artemia Salina ◽  
Toxicity Tests ◽  
Haemolytic Activity ◽  
Prymnesium Parvum ◽  
Unialgal Culture ◽  
Tlc Analysis ◽  
Layer Chromatography ◽  
Chloroform Methanol

Blooms of the marine flagellate Chrysochromulina have resulted in mortality of marine organisms in Scandinavian waters, including fish in aquaculture. Eight species of Chrysochromulina, namely C. apheles, C. brevifilum, C. ericina, C. hirta, C. leadbeateri, C. parva, C. polylepis, and C. simplex, isolated into unialgal culture, were examined for haemolytic activity and toxicity to the brine shrimp, Artemia salina. Haemolytic fractions were obtained from all species, but only C. polylepis cells were toxic to Artemia. Thin-layer chromatography (TLC) analysis in chloroform –methanol–water (75:25:4) and in chloroform–methanol (9:1) yielded up to six haemolytic spots. Except for one spot, these all occurred in extracts of the species examined, including Isochrysis sp., which was used as a control, C. polylepis, and the well-known fish killer Prymnesium parvum. The single unique haemolytic spot (Rf values 0.45 and 0.16 in solvents I and II, respectively) occurred in the extract from C. polylepis. When isolated by TLC, the contents of the single spot were toxic to Artemia. Key words: Chrysochromulina, toxicity, haemolytic, Artemia, thin-layer chromatography (TLC).

The polar lipids and free sugars of Frankia in culture

1983 ◽  
Vol 61 (11) ◽  
pp. 2834-2842 ◽  
Author(s):  
Mary F. Lopez ◽  
Carol S. Whaling ◽  
John G. Torrey
Keyword(s):  
Thin Layer ◽  
Thin Layer Chromatography ◽  
Paper Chromatography ◽  
Phosphatidyl Inositol ◽  
Free Sugars ◽  
Whole Cells ◽  
Cyanobacterium Anabaena ◽  
The Media ◽  
Layer Chromatography ◽  
Chloroform Methanol

To further the identification of characteristics common to Frankia strains, the phospholipids and sugars which are readily extracted with chloroform–methanol from whole cells were examined using nine strains of Frankia. Separation of extract components was achieved by thin-layer chromatography. In agreement with previous reports we have identified two phospholipids, phosphatidyl inositol and diphosphatidyl glycerol, in eight of the strains tested. All strains contained a glucose disaccharide which we have tentatively identified as trehalose on the basis of (i) comparative thin-layer and paper chromatography with standards, (ii) examination of the hydrolyzed product, and (iii) tests for reducing versus nonreducing sugars. In addition, a hexose with the chromatographic properties of glucose was observed in cultures grown on M6B complex medium. The presence of the phospholipids in Frankia strains was not affected by the age of the culture or the media on which they grew. However, the disaccharide was not present in cultures over 60 days of age, suggesting it is involved in metabolic processes. In addition, comparisons were made between extracts from Frankia and the nitrogen-fixing cyanobacterium Anabaena variabilis to determine if the glycolipids which are unique to Anabaena heterocysts are present in Frankia. These two organisms appear to have an unidentified lipid in common, but glycolipids comparable with those in Anabaena were not found in the Frankia cultures examined.

Alveolar and saccular lung phospholipids of the anaconda, Eunectes murinus

1978 ◽  
Vol 56 (4) ◽  
pp. 1009-1013 ◽  
Author(s):  
Charles F. Phleger ◽  
David G. Smith ◽  
Douglas H. Macintyre ◽  
Brian S. Saunders
Keyword(s):  
Surface Tension ◽  
Thin Layer ◽  
Thin Layer Chromatography ◽  
Lipid Extract ◽  
Two Dimensional ◽  
Surface Tensions ◽  
Methanol Extraction ◽  
Layer Chromatography ◽  
Chloroform Methanol ◽  
Standard Techniques

Phospholipids and their mode of synthesis in lung samples from the alveolar and saccular regions of an anaconda (Eunectes murinus) were investigated by standard techniques of chloroform–methanol extraction and two-dimensional thin-layer chromatography. The alveolar lung has six times as much phosphatidylcholine in its lung wash lipid extract as saccular lung. Phosphatidylcholine and sphingomyelin are the two principal phospholipids of the tissue of both lungs. Alveolar lung incorporates a higher percentage although a smaller total amount of [1-14C]acetate (54%) into phosphatidylcholine (including lysophosphatidylcholine), whereas saccular lung only incorporates 8% [1-14C]acetate into phosphatidylcholine (including lysophosphatidylcholine) and 60% [1-14C]acetate into sphingomyelin. Saccular lung synthesized 31% disphosphatidylglycerol from [1-14C]acetate; alveolar lung did not synthesize any. Surface tension plots of lung wash lipid extracts show slight surpellic activity with minimum surface tensions of 22 dyn/cm (1 dyn = 10 μN) for both alveolar and saccular lung, at 37 °C.

scholarly journals Isolation and Characterization of Antibacterial Actinomycetes from Soil Samples of Kalapatthar, Mount Everest Region

1970 ◽  
Vol 10 ◽  
pp. 173-182 ◽  
Author(s):  
Tara Devi Gurung ◽  
Chringma Sherpa ◽  
Vishwanath Prasad Agrawal ◽  
Binod Lekhak
Keyword(s):  
Antibacterial Activity ◽  
Minimum Inhibitory Concentration ◽  
Thin Layer ◽  
Broad Spectrum ◽  
Inhibitory Concentration ◽  
Inhibition Zone ◽  
Group Method ◽  
Mount Everest ◽  
Primary Screening ◽  
Isolation And Characterization

Seventy-nine Actinomycetes were isolated from soils of Kalapatthar (5545m), Mount Everest region. Twenty seven (34.18%) of the isolates showed an antibacterial activity against at least one test-bacteria among two Gram positive and nine Gram negative bacteria in primary screening by perpendicular streak method. Thirteen (48.15%) showed antibacterial activity in secondary screening. The result showed that three of the isolates, K.6.3, K.14.2, and K.58.5 were highly active with an inhibition zone e"20mm and broad spectrum antibacterial activity including two methicillin resistant Staphylococcus aureus (MRSA) strains. Minimum inhibitory concentration (MIC) of antibacterial metabolites of the isolate K.6.3 was 1mg/ml, and that of isolates K.14.2 and K.58.5 was 2mg/ml. Two spots were detected on thin layer chromatography plate from each of the metabolites which was completely different from the spot produced by vancomycin. The active isolates from primary screening were heterogeneous in their overall macroscopic, biochemical, and physiological characteristics through unweighted pair group method using average (UPGMA) cluster analysis. Delineation of the three active isolates showing potent broad spectrum antibacterial activity revealed that they belonged to distinct taxonomic groups.Key words: Antibacterial activity; Minimum inhibitory concentration; Thin layer chromatographyDOI: 10.3126/njst.v10i0.2957Nepal Journal of Science and Technology Vol. 10, 2009 Page: 173-182 

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