Review Of Dr. Reddy 's Laboratories

An Erlenmeyer flask was used to accommodate the largest volume of recrystallization solvent calculated and was cooled in an ice bath to increase the yield of crystals. The solid was collected by vacuum filtration and washed with a small amount of ice water. The product is then dried to a constant mass by use of an oven and weighed. A small amount of the unknown was compared to two samples of acetanilide and phenacetin for a melting point range to determine the identity. The temperature of the unknown was recorded when the first trace of liquid can be seen and when the unknown was completely liquid.

Aspirin, Caffeine and Salicylamide were extracted from an over-the-counter pain reliever (BC Powder). These components were separated by manipulating their solubilities by adjusting the acidity and basicity of the solution. By doing this, the three components were forced into conjugate acid (or base) forms, causing selective solubility in either an aqueous or organic solvent. These layers were then separated by use of a separation funnel. Once separated, the components extracted were characterized by measuring the melting point and performing a TLC analysis. Also, the recovered aspirin from the first part of the experiment was recrystallized and compared to that of the

The purpose of experiment three was to identify the unknown component in the drug Panacetin. The use of physical properties can help identify unknown compounds and estimate the degree of their purities. In this experiment, solubility in boiling water and melting point were used to determine if the unknown was acetanilide or phenacetin. Since both compounds are soluble in boiling water and insoluble in cold water, recrystallization was used to remove any impurities from the solid.

This experiment involved three steps: synthesis of aspirin, isolation and purification, and the estimation of purity of the final product. The synthesis involved the reaction of salicylic acid and acetic anhydride in the presence of a catalyst, phosphoric acid, H3PO4. When the aspirin was prepared, it was isolated and filtered. The percentage yield of the synthesis was calculated to be 78.42%. The experimental melting point range of aspirin was determined to be 122 -132°C. Due to its wide range, and lower value than that of the theoretical melting point of 136°C, it was

The filter paper, holding the aspirin crystals, was removed from the funnel and was left to dry before being weighed. Once the aspirin crystals were weighed, the theoretical yield and the percent yield of the experiment were calculated. The procedure was repeated once more using the same steps.

Although some agar plates were hard to see if the streptomycin had a definitive zone of inhibition. Ampicillin, erythro-mycin, penicillin, sulphafurazole was ineffective with no inhibition zone.

During this experiment, guaifenesin was isolated and synthesized through a reflex process, which both heated the mixture and preserved the solid. Two Guai-Aid cough tablets, each containing 400 mg of guafenesin each, were used. The synthesis of guaifenesin resulted in a 23.7% yield based on the theoretical value of .6207 of guaifenesin given the limiting reactant, 2-methoxyphenol. The isolation of guafenesin resulted in a 5.38% yield due to the fact the isolation was completed from two 400mg tablets of guaifenesin. HNMR and a melting point test were both used to successfully confirm that guaifenesin was the product of the synthesis and isolation methods through the location of the peaks on the spectra and the comparison of melting points to the literature value.

The purpose of this report is to analyse the growth of the bacteria known as Citrobacter Freundii as well as distinguishing what antibiotics effect its growth. This will be done so by answering the following question after completing its associated experiments. This question includes: what antibiotics are most effective in denaturing the bacteria? It has been predicted that chloramphenicol will be the most effective due to the fact that its medical uses are treating meningitis which is an infection caused by Citrobacter freundii. After conducting the experiments it was found that the chloramphenicol antibiotic was the most effective in denaturing the bacteria, although streptomycin was also affective. However, none of the other antibiotics were able to halt the growth of the bacteria.

The phenacetin product collected from the Williamson Ether synthesis (Product A) had an average melting point of 132.0 ˚C -133.5 ˚C, while Amide Synthesis product (Product B) had an average melting of 120.0 ˚C -124.5 ˚C. The MP of a pure substance usually has a range 1-2 ˚C and no significant MP depression. As noted from the data, Product B had a quiet significant depression of 10 ˚C and a range of 5 ˚C, while Product A had a range of 1 ˚C; comparing the melting point data of both products, it can be concluded that Product A has a higher purity. As evident from the data collected from Melting Point analysis, it is highly probable that the product B was contaminated by foreign products.

The aim of this investigation was to find out which antiseptics were most effective at preventing the growth of bacteria.

Anti-infection agents have spared countless furthermore added to the expansion in future. They are essentially delivered by the fermentation of fungi (e.g., Penicillium) and bacteria (e.g., Actinomycetes). Specifically, 80% of anti-infection agents are sourced from the family Streptomyces and uncommon actinomycetes, for example, Actinomadura, and just the 20% is created by fungal species (Lo Grasso,

Staphylococcus aureus (S. aureus) is a spherical bacteria which is known to produce a cytotoxin called Panton-Valentine leucocidin (PLV) which destroys leukocytes, and kills tissue (Lina et al., 1999). Five percent of strains of Staphylococcus are known to produce the disease-causing toxin (Lina et al., 1999), but though the amount of PLV-producing strains is somewhat small, the strains which produce PLV are apparently resistant to vancomycin, an antibiotic commonly used to treat staph infections (CDC, 2002). The first recorded case of S. aureus resistance to vancomycin was a reduction in sensitivity to the antibiotic observed in Japan, and has since spread to the United States (CDC, 2002). The most common source of infection of these drug-resistant bacteria are actually in hospitals, wherein the patients are exposed to the bacteria and subsequently infected (CDC, 2002).

The study of two unknown microorganisms was completed by using methods taught in the microbiology laboratory. The basis of the study was identification of those two microorganisms. Identification of the microorganisms is important in many aspects of medicine. Some of these include source of infection, proper treatment, and which antibiotics are effective against the microorganism present.

One person each in a team of four heavily inoculated two Mueller-Hinton agar plates with one of the cultures listed by aseptic transfer from a broth culture using a sterile cotton swab. Each plate was marked off into four segments, a total of eight sectors. One McFarland standard disk containing one of the eight antibiotics tested was placed, using

Subsequently, 10mL of 3.5% H2O2 were added dropwise to the reaction mixture and was stirred for 20 minutes before heating to boiling at 80°C for 5 minutes. The reaction mixture was then taken off heat and allowed to cool undisturbed in an ice-bath for 30 minutes. Suction filtration was performed after to collect the crystals from the chilled solution The product was then washed with chilled 95% ethanol (2 x 15mL) and followed by diethyl ether (2 x 10mL). The crude product was then left to dry before recording the yield. 20mg of the crude product is then accurately weighed out and dissolved in deionized water in a 25mL volumetric flask. Deionized water was added to the volumetric flask to the mark and the UV-vis absorption spectrum of the crude product was recorded.