In bottom to top approach, chemical reduction is the most common scheme for syntheses of silver nanoparticles, .Different organic and inorganic reducing agents, such as sodium borohydride (NaBH 4), sodium citrate, ascorbate, elemental hydrogen, Tollen's reagent, N,N-dimethyl formamide (DMF) and poly (ethylene glycol) block copolymers are used for reduction of silver ions (Ag +) in aqueous ...
Oct 28, 2010· Results. The ethanolic extracts of 51 species inhibited Escherichia coli, and 114 ethanolic extracts inhibited Staphylococcus aureus. In contrast, only 30 aqueous extracts showed activity against E. coli and 38 extracts against S. aureus. The MIC concentrations were mostly very high and ranged from 0.008 to 256mg/ml, with only 36 species showing inhibitory concentrations of <4mg/ml.
The zone of inhibition of the plant extract at the concentration of 62.5mg/ml was significantly different when compared to 500 mg/ml of the plant extract for the tested bacteria S. aureus, E. coli, K. pneumonia, S. typhi, and Citrobacter (p<0.05) and the zone of inhibition of the plant extract at 500 mg/ml was significantly different from that ...
The extract protein concentration obtained ranged from ≈0.5–1.5 μg μl –1 (4‐day‐old seedlings) to 2.5–5.5 μg μl –1 (7‐day‐old seedlings) and 5–10 μg μl –1 (adult plant leaves). The amount of protein loaded per lane was different depending on which phy was to be detected or which tissue was extracted, as specified in ...
In many parts of the world, medicinal herbs are widely used because people cannot afford the wonder drugs available on the market. The knowledge of using healing herbs is passed on from one generation to another. Even your grandparents used to rely on medicinal herbs when medical aid was not available.
May 07, 2015· The present invention relates to a method for preparing a granule or a pill containing a plant, medicinal herb or traditional oriental medicine decoction extract, comprising the steps of: (a) injecting a powdered plant, medicinal herb or traditional oriental medicine decoction extract into a fluidized-bed device and spraying purified water or a solution of the same type of extract as the ...
To provide an extract or other substance that can impart not only bitterness and aroma but also taste elements such as koku and robustness without increasing astringency or harshness, and to provide a beverage having superior koku and robustness. Increasing hop-derived polyphenols, particularly trimeric proanthocyanidin makes it possible to provide beverages with koku and robustness without ...
At the concentration used, Fast Green stains the tissues within 10–15 s, so it is best to test the procedure on one or two slides before staining your entire set. In plant tissues stained with this method, Safranin O appears brilliant red in chromosomes, nuclei, lignified, suberized, or cutinized cell walls.
A stock solution of plant aqueous extract was prepared by dissolving 100 mg of extract in 1 ml of sterile distilled water. Likewise, for the ethanol extract, 100 mg of extract was dissolved in 1 ml of 10 % Tween-20 rather than the original solvent (i.e. Dimethyl sulfoxide), and so the initial concentration of the plant extract (100 mg/ml)
Therefore, methods for isolation of nuclei from intact plant cells and tissues have been developed for a number of plant species using embryos [25, 26], seed coat, cultured plant cells, meristematic root tissues or leaf tissues [30, 31]. Most of the isolation methods use the same steps of the procedure, including tissue disruption, filtration ...
Protocol a simple method for extracting - Plant Methods. I understand that you want to prepare a stock solution s s concentration from the plant extract to be examined by dilutions in a final concentration with keeping the percent of DMSO as 0 5 . Minimum Inhibitory concentration MIC Broth dilution .
I understand that you want to prepare a stock solution (s.s.) concentration from the plant extract to be examined by dilutions in a final concentration with keeping the percent of DMSO as 0.5%.
Larvicidal activity of aqueous and ethanol extract of C. didymobotrya was evaluated by using WHO method. Twenty five 2nd, 3rd, 4th and pupal stage was released in to 250 mL of glass beaker individually. In each beaker, concentration of aqueous and ethanol extract was maintained at 10 000, 1 000, 100, 10 and 1 mg/L concentration with the final ...
Prepare antimicrobial agent stock solutions at concentrations of at least 1000 μg/mL (example: 1280 μg/mL) or 10 times the highest concentration to be tested, whichever is greater. Because microbial contamination is extremely rare, solutions that have been prepared aseptically but not filter sterilized are generally acceptable.
Jul 22, 2008· The invention claimed is: 1. A method for preparing an aqueous extract of plants, comprising: a) decontaminating the plants, the plants being one or more of a plant part or one or more of plant parts of various plant species; b) comminuting the plants; c) treating the comminuted plants with laser radiation for a suitable time using a laser radiation device comprised of a red linear laser …
Applying the present standardized method, the extracted DNA concentrations varied with the different plant species used in the present work (Table 2).The yield of isolated DNA ranged from 2.238 ηg/mg of seeds in case of Cucurbitales maxima to 24.957 ηg/mg of seeds in the case of Lupinus lupinus. The other classical CTAB method employed (Doyle and Doyle 1990) also produced comparable range of ...
GAE/gm of dry extract) and strong DPPH radical scavenging activity (IC 50 0.62 mg/gm of dry extract) whereas S. arvensis showed moderate antioxidant activities (Seal, 2011). Thus, the presence of an appreciable amount of ascorbic acid, flavonoids and phenolic acids in these plants …
Extraction techniques of Medicinal plants Extraction, as the term is used pharmaceutically, involves the separation of medicinally active portions of plant or animal tissues from the inactive or inert components by using selective solvents in standard extraction procedures. The products so obtained from plants are relatively
Antioxidant activity: Blois 17 method was used to determine the free radical scavenging activity of the plant extract by using DPPH (2,2-diphenyl-1-picrylhydrazyl). Briefly, 0.2 mM DPPH solution was made using methanol. Ascorbic acid was taken as standard and 5 different concentrations (200, 400, 600, 800 and 1 mL) were taken to make the standard curve.
The extract of the solute in flow rate of 1 ml/min at the wavelength 210 nm and methanolic extract showed the antioxidant activity and powerful oxygen free radicals scavenging activities and the IC50 for the E. intermedia plant was near to the reference standard ascorbic acid. The HPLC method was useful for the quantitative purpose of ephedrine ...
METHODOLOGY 3.1 Collection and Preparation of Stock Plant Extract The tomato (Solanum lycopersicum) will be purchased at Bankerohan Public Market, Davao City. The tomato will be washed thoroughly several times and sliced thinly. The seeds of the tomato will be discarded. The tomato will be oven dried for 3 days at 70°C and will then be ground until its powdered form.
Nevertheless, water extracts of A. discoridis developed the highest antimicrobial activity against all test microorganisms. Furthermore, acetone extracts of A. discoridis and R.chalepensis showed noteworthy inhibitory effects to most test microorganisms with mean inhibition zone values ranging from 15.7±1.2 to 23.7±2.5 mm and from 16.7±0.6 to 18.7±1.5 mm, respectively.
Background. Protein extracts obtained from cells or tissues often contain interfering substances, which must be removed for preparing high-quality protein samples [].In particular, plant tissues contain a diverse group of secondary compounds, such as phenolics, lipids, pigments, organic acids, and carbohydrates, which greatly interfere with protein extraction and proteomic analysis [].
Nov 27, 2013· Extracts 8, 38 and 43 demonstrated the lowest IC 50 range, indicating a higher amount of NAI in the given plant extract or the presence of potent NAI component(s) that may be active even at a lower concentration. Extracts were tested at µg/mL concentrations, unlike Zanamivir and Oseltamivir, which were tested at nanomolar levels.
Hauser supplies companies such as Rexall with herbal extracts. Hauser's extraction process is a trade secret, but Lenoble says it "emulates a tea cup"—plant material is put into a big vat with a solvent of ethanol and water, known as a menstruum, to draw out the plant's constituents; Lenoble says their low-heat process combined with the watered-down ethanol makes for a gentler solvent.
Extraction methods for preparation of bioactive plant extracts Authors: Waghmare Deepak Harishchandra 1, Deshmukh Arti Madhukar 2 Savitribai Phule Pune University, Pune 1 Vasantrao Naik Marathwada Agriculture University, Parbhani 2 Extraction is the crucial first step in the analysis of medicinal plants, because it is necessary to extract the desired chemical components from the plant ...
The plant extract was obtained from Barij essence co. The type strains of C.albicans were prepared from (PTCC 90028) collections. 45 clinical isolates of C.albicans that were confirmed by microbiological methods used in the tests. Inhibitory effects of the Extract analyzed by …
The ability of the extracts to annihilate the DPPH radical (1,1-diphenil-2-picrylhydrazyl) was investigated by the method described by (Blois, 1958). Stock solution of the whole plant extracts was prepared to the concentration of 1 mg/ml. 100 µg of each extracts were added, at an equal volume, to methanolic solution of DPPH (0.1 mM).
Kief is generally considered a lower-quality extract, but some top-flight extractors can produce an extremely clean and flavorful product using the dry sieve method. THC content can range from 20 percent to 60 percent.
Broth micro- or macro-dilution is one of the most basic antimicrobial susceptibility testing methods. The procedure involves preparing two-fold dilutions of the antimicrobial agent (e.g. 1, 2, 4, 8, 16 and 32 µg/mL) in a liquid growth medium dispensed in tubes containing a minimum volume of 2 mL (macrodilution) or with smaller volumes using 96-well microtitration plate (microdilution) ().
Where X 1 refers to the weight of extract after evaporation of solvent and X 0 refers to the dry weight of the plant powder before extraction.. Preparation of Inoculum. The antimicrobial properties of plant extracts were tested against Gram-positive bacteria [Bacillus cereus 10451 (BC), Staphylococcus aureus 10786 (SA)], Gram-negative bacteria [Escherichia coli GIM1.708 (EC), Salmonella ...
The hot water extraction method is by and far the most widely employed extraction method in producing powdered extracts for medicinal use. What is commonly believed to involve only a single step of extraction using water, actually occurs in two steps (as shown above), one involving hot water and one involving ethanol (alcohol).
using sterile cork borer. Stock solution of each plant extract was prepared at a concentration of 1 mg/ml in different plant extacts viz. Methanol, Ethanol, Petroleum Ether, Water. About 100 µl of different concentrations of plant solvent extracts were added sterile syringe into the wells and allowed to diffuse at room temperature for 2hrs.