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History of herbal medicine easy
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Although medicinal plants have been widely used since the ancient times, the identity of the compounds that showed the desired therapeutic effect remained unknown until a few decades back. Development in the field of medicinal chemistry and pharmacology led to their structural elucidation and further helped in understanding their biological activities in the human body. The chemists synthesized these compounds thus reducing the cost of their production. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2658564/pdf/embor200912.pdf But there have been reports of adverse effects that synthesized drugs cause which has renewed the interest in the use of natural compounds (reference). Andrographolide is a bitter compound extracted from the leaves and stem of an herbaceous plant called Andrograhis paniculata. It is a diterpene lactone showing multifarious activities like anti-pyretic, anti-inflammatory, antioxidant,anticancer,(u1pdf)and hepatoprotective http://ict.sagepub.com/content/6/3/271.full.pdf+html. Water soluble andrographolide sulfonate has been recently synthesized exerting anti-sepsis action in mice. http://www.sciencedirect.com/science/article/pii/S1567576912002652.
Considering the importance of andrographolide there is the need to develop extraction techniques to extract this biomolecule from natural sources. Traditional extraction techniques have the drawbacks of longer extraction time, higher extraction temperature, increased solvent consumption and mass transfer resistance. Hence novel extraction techniques like ultrasound assisted extraction (UAE), microwave assisted extraction (MAE), supercritical fluid extraction (SCFE) and accelerated solvent extraction have been developed which overcome these pitfalls http://www.sciencedir...
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... from Sigma-Aldrich. Acetonitrile and acidified water were used as the mobile phase for HPLC. Acetonitrile was of HPLC grade and ethanol used as the solvent was of AR grade. These solvents were purchased from High media, Mumbai, India for the experiments. Distilled water used as one of the mobile phase was obtained from Millipore Milli Q 50 HPLC grade.
2.2 Analysis of andrographolide
Separation of andrographolide from its extract was done using HPLC (Agilent 1260 infinity high performance auto sampler) equipped with C18 column. Mobile phase used for HPLC analysis comprised of acetonitrile and acidified water in the ratio 60:40 v/v. Isocratic elution was used to
perform HPLC analysis where the flow rate was set at 1.0 mL/min throughout the run with an injection volume of 5µl. The peak for andrographolide was detected at 223 nm with a retention time of 7.2 minutes.
Every 5 minutes, a small amount of mixture was dissolved in acetone (0.5 mL) and was spotted onto a thin layer chromatography (TLC) plate, which contained an eluent mixture of ethyl acetate (2 mL) and hexanes (8 mL). The bezaldehyde disappearance was monitored under an ultraviolet (UV) light. Water (10 mL) was added after the reaction was complete, and vacuum filtrated with a Buchner funnel. Cold ethanol (5 mL) was added drop-by-drop to the dried solid and stirred at room temperature for about 10 minutes. Then, the solution was removed from the stirrer and place in an ice bath until recrystallization. The recrystallized product was dried under vacuum filtration and the 0.057 g (0.22 mmol, 43%) product was analyzed via FTIR and 1H NMR
The complete experimental procedure is available in the General Chemistry Laboratory Manual for CSU Bakersfield, CHEM 213, pages 20-22, 24-25. Experimental data are recorded on the attached data pages.
The objective of this experiment was to perform extraction. This is a separation and purification technique, based on different solubility of compounds in immiscible solvent mixtures. Extraction is conducted by shaking the solution with the solvent, until two layers are formed. One layer can then be separated from the other. If the separation does not happen in one try, multiple attempts may be needed.
Henderson, L., Yue, Q. Y., Bergquist, C., Gerden, B., & Arlett, P. (2002). St John's wort (Hypericum perforatum): drug interactions and clinical outcomes. British journal of clinical pharmacology. 2002; 54(4):349-356.
The purpose of this experiment was to learn and preform an acid-base extraction technique to separate organic compounds successfully and obtaining amounts of each component in the mixture. In this experiment, the separation will be done by separatory funnel preforming on two liquids that are immiscible from two layers when added together. The individual components of Phensuprin (Acetylsalicylic acid, Acetanilide, and Sucrose as a filler) was separated based upon their solubility and reactivity, and the amount of each component in the mixture was obtained. Also, the purity of each component will be determined by the melting point of the component.
Once the mixture had been completely dissolved, the solution was transferred to a separatory funnel. The solution was then extracted twice using 5.0 mL of 1 M
..., and is immiscible with water. Since there was not clear distinct two layers after steam distillation, extraction was used to separate the eugenol from water thus, steam distillation is not an effective way to isolate eugenol by itself. In order to determine how pure the isolated eugenol was, TLC was performed and compared to the standard and 1H NMR of the isolated eugenol and standard were compared to conclude that the extracted compound was eugenol with some impurities.
In this experiment, a mixture of three substances (benzoic acid, 2-naphthol, and 1-4 dimethoxybenzene) will be separated based off acidity strength using the liquid-liquid extraction technique through a separatory funnel. Benzoic acid and 2-napthol will be converted into ionic salts when reacting with their appropriate bases (sodium bicarbonate and sodium hydroxide). Both ionic salts will then form solids through the addition of acidic HCl. Neutral 1,4 – dimethoxybenzene forms a solid through the evaporation of ether. Each compound will then be purified through recrystallization, using the processes of dissolving the solid in either water or methanol, and isolating the solid through vacuum filtration. After a week of evaporation, the compounds will then be examined for both
After performing the first Gas Chromatography, we took the organic layer, and mixed it with saturated Sodium Hydroxide. We performed this step to remove the (-OH) group from the Eugenol. The purpose was to make the water as a product, which can also be used as a solvent for the Eugenol that was ionized, for the two substances Acetyl Eugenol and Beta Caryophyllene. Again, we see the density differences in the solvents; we were able to take the organic layer. Finally, we transferred the layer into the beaker and dried, to perform the Gas Chromatography
The choice of mobile phase depends on the chemical nature of the compound of interest and could be purely organic, inorganic or a mixture of both in gradient. Most commonly used mobile phases are organic solvents like acetonitrile or methanol. Some HPLC analysis require the use of water free solvents as mobile phase and in such cases acids like formic acid, phosphoric acid, trifluoroacetic or salts which will assist in separation of components in the sample are used.
Materials and Methods: An ion exchange chromatography column was obtained and set up for purification with the addition of 0.5 ml ion exchange matrix. 1 ml
Within the andragogical model described by Knowles, Holton, and Swanson (2015), adults need learning experiences that are different than those found in the pedagogical model. Instead of waiting for experiences that are directed and controlled by a teacher, adults need to have a clear rationale and understanding for the learning, feel past experiences are valuable, and have a developed internal system for motivation in order to help a learning experience be successful. The connection and orientation to the learning task, the readiness to learn, and self-concept are other important ideas to adult learning.
In this experiment, lipids from ground nutmeg are extracted using a combination of solvents and identify the lipids through chromatography. The purpose of using solvent combinations is to elute the lipids based on their polarity to binding of the silica gel. The chromatography is performed on a silica gel plate and the use of iodine to visualize the lipids. By calculating the Rf values for each compound and comparing them to the known lipids, we are able to distinguish the lipids within the grounded nutmeg.
Herbal medicines are sold in different ways from tablets, teas, extracts, capsules, powders, and fresh or dried plants. Many consumers believe that these products are safe and free of harm due to the labeling of the product with words such as “all natural.” The downside of taking these “natural” medicines are some ingredients can cause harm to a consumer’s health. According to the U.S .National Library of Medicine, some herbs, such as comfrey and ephedra, can cause serious harm. It is also reported that herbal
Frequently a person believes that herbal medicine is more naturally safe and soothing than drugs. Nevertheless, there’s no reasonable defense about this. Though many consumers trusted herbal medicine much more than the synthetic medicine because it’s safe and effective, but like anything else, it has its own limitations too. There are several hostile issues related to herbal medicine that has been quite alarming. Notwithstanding, majority of the most popular herbs are at least nearly safe.