scholarly journals ANTIBACTERIAL ACTIVITY AND THIN LAYER CHROMATOGRAPHY PROFILE Muntingia Calabura LEAF EXTRACT AS A MATERIAL CANDIDATE HAND SANITIZER

2018 ◽  
Vol 11 (1) ◽  
pp. 43
Author(s):  
Santy Pristianingrum ◽  
Baiq Lely Zainiati ◽  
Iwan Doddy Dharmawibawa

Abstract : the utilization of antibacterial active substances from several plants is increasingly not only as the ingredients of medicine, but its utilization is also utilized for an antibacterial ingredient for preventive action, one of them is hand sanitizer material. This research focused to find the antibacterial active substances alternative from Muntingia calabura leaves extract. The data were analyzed descriptively including the inhibitory of ethanol absolute extract and ethanol 95% of M. Calabura against isolate clinical bacteria by Kirby Bauer method and the type of coumpund that contains in M.calabura leaf by thin layer chromatography utilizingeluen n-hexan- Methanol. Etanol absolute extract M.calabura leaf showing the average inhibition zone against Pseudomonas aeruginosa 15.67 mm, Staphylococcus aureus 19.33 mm and Escherichia coli 13 mm. While, The etanol extract 95% showing higher inhibition Pseudomonas aeruginosa 19.67 mm, Staphylococcus aureus 19.33 mm and Escherichia coli 16.67 mm. This inhibitory zone was slightly lower than chlorhexidine gluconate with an average of 20-24 mm against the three bacteria that utilized in the test but belongs to the strongly sensitive category for natural materials according to Mukherjee (1988). From thin layer chromatography profile with eluen n-hexan: methanol found three compounds that were in the range of Rf value 0.4; 0.5 and 0.7. The Conclusion for this study is the bioactive material from etanol 95% extract M.calabura leaf can be optimized to the hand sanitizer active compound candidate.

Food systems ◽  
2021 ◽  
Vol 4 (1) ◽  
pp. 26-30
Author(s):  
N. V. Kupaeva ◽  
E. R. Vasilevskaya ◽  
L. V. Fedulova ◽  
E. A. Kotenkova

Plants are a rich source of effective non-toxic biologically active substances. Various physicochemical methods of analysis are used for evaluation of plant antioxidant activity. Composition of ethanol extracts of red, yellow and white onion husks, dried rosemary, basil, and chaga were studied by high performance thin layer chromatography (HPTLC) method. The antioxidant activity of the obtained fractions on a chromatographic plate was assessed by subsequent DPPH screening. The extracts red and yellow onion husk and rosemary demonstrated the highest antioxidant activity, variability of the qualitative composition and similarity of antioxidant profiles, while extract of white onion husks did not contain any antioxidant classes. Intensive spots with Rf of 0.13-0.97 were observed along the whole chromatogram track corresponding to red onion husks. It was also found that all tested extract, excepting white onion husk and chaga, contained spots with varying degrees of intensity in the Rf range of 0.96-0.98, which corresponded quercetin Rf value.


2020 ◽  
Vol 10 (2) ◽  
pp. 82
Author(s):  
Fatemeh Samieerad ◽  
Nematollah Gheibi

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


2020 ◽  
Vol 19 (5-6) ◽  
pp. 148-154
Author(s):  
Vali A. Sahratov ◽  
Tamara L. Malkova ◽  
Ludmila N. Karpova ◽  
Anna A. Pospelova

The State Pharmacopoeia of the XIV edition defines the approach for the assessment of the quality of medicinal plant materials, it deals with the identification of the main groups of biologically active substances by thin layer chromatography. According to this approach, the analysis of some types of medicinal plant materials as a part of some objects of plant origin was carried out. The article presents the quality assessment algorithm as examplified by peppermint leaves (Mentha piperita L.), which are part of a variety of plant object.


Author(s):  
L. Chervyakova ◽  
T. Panchenko ◽  
O. Tsurkan ◽  
N. Adamenko

Goal. To develop a method for the determination of imidacloprid, clothianidin, prothioconazole and tebuconazole in the treatment seeds of wheat and barley. Methods. Active substances were determined by thin layer chromatography (TLC). Mathematical-statistical method for evaluate the linear range of the dependence of the area of the chromatographic zone on the amount of active substance was used. Results. The determination of pesticides includes a number of basic stage: characteristic the matrix by the ratio of the content of coextracting substances, that interfere with the determination, and the content of pesticides; classification of pesticides by polarity in according to the dipole moment (µ, D); extraction from the analyzed sample by organic solvent with corresponding of the dielectric constant, ε; purification; qualitative and quantitative determination. In the case of the analysis of treatment seeds, in which the amount of pesticides is much greater than coextracting compounds, the stages of classification and purification are excluded from the analysis. The extraction is carried out with ethanol. Qualitative determination of pesticides is carried out on plates with a thin layer of adsorbent (silicagel) in the mobile phase (mixture of hexane and ethanol, ε = 7.49) with using corresponding reagents. Silver ammonia (AgNO3) solution and followed by UV irradiation of the chromatogram is used for identification halogen-containing pesticides (zones of localization of compounds are formed dark spots of reduced silver). Pesticides containing donor atoms of sulfur, nitrogen, oxygen, identify by bromphenol blue (BPB) and subsequent bleaching of the background with an solution of citric acid (zones of localization of compounds are formed blue spots form on a light background). The active substances are identified with the corresponding Rf of the zones localization. Quantitatively of active substances is determined by the calibration dependence of the area of compound’ chromatographic zone on its quantity. For all four compounds, this dependence is linear in the concentration range of 0.20 — 0.80 µg and is described by the regression equation for: imidacloprid y = 6.25x + 5.45; for clothianidine y = 11.65x + 6.70; for prothioconazole y = 28.7x + 2.05; for tebuconazole y = 13.00x + 7.00. In all cases, the correlation between the indicators is estimated as strong (r = 0.99). Conclusions The algorithm for assessing the completeness of the treatment of wheat and barley seeds is an express control method and using the thin layer chromatography method allows to determine four active substances in one sample during one analysis with high accuracy (relative error of less than 5% at n = 5, P = 0.95) excluding laborious experiment.


2021 ◽  
pp. 15-18
Author(s):  
L. Cherviakova ◽  
T. Panchenko ◽  
O. Borzykh

Goal. The choice of a chromatographic method and the development of a method for the analytical determination of imazethapyr, imazamox, imazapyr in herbicide preparative forms in the joint presence. Methods. Active substances were analyzed by thin layer chromatography. The linear range of the dependence of the area of chromatographic zones on the amount of active substance was assessed by a mathematical-statistical method. Results. Determination of pesticides by thin-layer chromatography includes the main stages: classification of pesticides by polarity; extraction of active substances from the analyzed sample; chromatographic separation, detection and quantification. The decisive factor in the analysis stages is the dipole moment (μ, D), which characterizes the polarity of the compounds. Imazethapyr, imazamox and imazapir are polar compounds (μ≥6, D) with the corresponding values: 6.1; 6.4 and 6.8 D. Extraction of active substances is carried out with ethanol. Qualitative determination — in a thin layer of adsorbent silica gel in the mobile phase: a mixture of ethanol with acetic acid in a ratio of 4 : 1.5. Identify compounds at the wavelength of the spectrum λ 254 nm and using the developing reagent silver ammonia. The calibration dependence of the area of the chromatographic zone of the compound on its amount is linear in the detection range of 0.30—1.30 μg and is described by the regression equations for: imazethapyr S = 12.345 C + 0.7778, R2 = 0.99; imazapyr S = 9.3671 C + 1.081, R2 = 0.99; imazamox S = 7.6234 C + 1.4462, R2 = 0.98. The equation is used to quantify the active ingredients in the chromatogram. Conclusions. The use of the method of thin layer chromatography makes it possible to select selective conditions for the analysis of imazethapyr, imazamox, and imazapyr in the presence of herbicides in preparative forms. The developed technique is an express method of control and provides determination of active substances in the course of one analysis with high accuracy (relative error is less than 5% at n = 5, P = 0.95). The analytical support of the developed and patented method allows for analytical control of active substances of the imidazolinone class in the formulation of pesticides by analytical and toxicological laboratories, testing services without the use of expensive devices.


2014 ◽  
Vol 58 (10) ◽  
pp. 6324-6327 ◽  
Author(s):  
Tatsuya Tada ◽  
Tohru Miyoshi-Akiyama ◽  
Rajan K. Dahal ◽  
Shyam K. Mishra ◽  
Kayo Shimada ◽  
...  

ABSTRACTStenotrophomonas maltophiliaIOMTU250 has a novel 6′-N-aminoglycoside acetyltransferase-encoding gene,aac(6′)-Iak. The encoded protein, AAC(6′)-Iak, consists of 153 amino acids and has 86.3% identity to AAC(6′)-Iz.Escherichia colitransformed with a plasmid containingaac(6′)-Iakexhibited decreased susceptibility to arbekacin, dibekacin, neomycin, netilmicin, sisomicin, and tobramycin. Thin-layer chromatography showed that AAC(6′)-Iak acetylated amikacin, arbekacin, dibekacin, isepamicin, kanamycin, neomycin, netilmicin, sisomicin, and tobramycin but not apramycin, gentamicin, or lividomycin.


2019 ◽  
pp. 1-11
Author(s):  
R. Abdulaziz ◽  
M. H. Usman ◽  
U. B. Ibrahim ◽  
B. M. Tambari ◽  
A. Nafiu ◽  
...  

The aim of study was to evaluate the antibacterial activity of Cochlospermum tinctorium against ten (10) strains of antibiotic resistant food-borne pathogens Staphylococcus aureus and Listeria monocytogene. Ten (10) strains of antibiotic resistant food-borne pathogens Staphylococcus aureus and Listeria monocytogene procured from Microbiology Research Laboratory Usman Danfodiyo University Sokoto. The roots of Cochlospermum tinctorium were collected from the rock side in Dambu Gomo, Zuru Local Government Area of Kebbi State, Nigeria. The roots were washed, air-dried and milled to powder using mortal and pestle and sieved to obtained fine powder. Maceration was used for extraction using methanol as solvent. The antibacterial activity of the plant was determined on Mueller Hinton agar using agar well diffusion method. Minimum concentration (MIC) and minimum inhibitory concentration (MBC) of plant extract was also determined. Thin layer chromatography and column chromatography was employed for separation and fraction of different compounds in the plant extract. The fractions were screened for antibacterial activity and active fractions having high antibacterial activity were subjected Gas Chromatography Mass Spectoscopy (GC-MS) analysis. The result of methanol extraction yield 5.17% extracts. The methanol extract of Cochlospermum tinctorium was effective in inhibiting the isolates at high concentration of 10 mg/mL. The results thin layer chromatography revealed four spots with Rf values 0.02, 0.37, 0.44 and 0.80 respectively. The GC-MS analysis of the active methanol extract of Cochlospermum tinctorium root powder revealed the existence of major peaks 1-(+)-Ascorbic acid 2,6-dihexadecanoate (R.T: 13.666), Diethyl phthalate (R.T: 10.440), Undecyl acetate (R.T: 10.007), 3-tetradecanone (R.T: 9.793), 3-hexadecanone (R.T: 12.427). It therefore concluded that the root of Cochlospermum tinctorium has immense potential to be used in the area of pharmacology as it possess antimicrobial activity against the antibiotic resistant food-borne pathogens, thus could be exploited as alternative antimicrobial drugs.


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