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A level thin layer chromatography sample report essay
A level thin layer chromatography sample report essay
A level thin layer chromatography sample report essay
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In this lab, Thin Layer Chromatography was used to identify the components of a certain drug. To do this, the compound in question, Motrin was tested against six standards in three different solvents. The three solvent were hexanes, ethyl acetate, and 75% ethyl acetate and 25% hexane; the solution of 75% ethyl acetate and 25% hexane was determined to be the best solvent. This is due to the larger variance in RF values. The six standards that Motrin was tested against were Aspirin, ibuprofen, acetaminophen, naproxen sodium, caffeine and a caffeine and ibuprofen mixture. To determine which standard was present in the chosen drug, the retention factors, or RF, were calculated. A UV light was also used to see the distance each sample traveled in …show more content…
A source of error in this lab could have resulted from the use of a different solvent at this point. The other solvents resulted in a lower range of retention factors, therefore making it harder to determine which one were similar and present in the drug. The use of 75% ethyl acetate and 25% hexane allows for the RF values to be distinguishable and conclusions can be made. The conclusion made about Motrin was that it consisted of Ibuprofen. This was determined by the RF values on the third TLC plate. The retention factor of Motrin was closest to Ibuprofen. The values for these two were 0.64 and 0.65. The caffeine and ibuprofen mixture was also close at 0.66 but since there was a second value of 0.08, this mixture is not in Motrin. Also, Aspirin was found not to be in Motrin based on the retention factor of 0.60. The RF values in this lab were imperative to figuring out what the drug consisted of, so if the measurements or calculation were off, identification may have not been possible. If measurements were off, the retention factors would not be correct, therefore resulting in an error and wrong conclusion about the drug in
Thorough analysis of the graph displayed enough evidence suggesting that an increase in substrate concentration will increase the height of bubbles until it reaches the optimum amount of substrate concentration, resulting in a plateau in the graphs (figure 2). Hence; supported the hypothesis.
The analysis is therefore one of the most effective methods of ensuring that each drug being prescribed to patients is safe. It also ensures that all drug components are understood in terms of their structure and chemical behavior. This understanding is very important in the manufacture of drugs and other pharmaceutical products.
After obtaining three fraction samples of hexane, heptane, and the mixture of the two into three separate vials, gas chromatography was performed to find the relative composition of each of the three samples. For the first vial containing pure hexane, a ratio of 66.26% hexane to 33.74% heptane was determined and had a boiling point range of 69.2-76.4°C during simple distillation. The second vial containing both hexane and heptane was determined to have the ratio of 40.15% hexane and 59.85% heptane and a boiling point range of 78.2-89.0°C. The third vial containing only heptane had a
The aspirin crystals were packed into 3 small capillary tubes to ensure that they are compressed so as to prevent any air gaps. Subsequently, the aspirin crystals that are in the 3 capillary tubes are placed into the melting apparatus and the temperature range was recorded. Since the range is quite far from the theoretical value of 140°C, aspirin's purity attained was low due to impurities present. One potential reason is because of the swift cooling. When the aspirin is left to cool, the crystal lattices will form too rapidly which will surround other molecules thus making the aspirin impure. Another reason could be because the recrystallized aspirin has not dry completely and there might me left over solvent that will affect the temperature range of the aspirin.
Although there are very less situations which are reported with respect to the dual paracetamol peaks with sustained-release preparations. 2-5 It was studied in very detail. But it was clear-cut from the empty tablet blister packets present at the situation scene that the patient had taken just the basic-preparation paracetamol. The chance of another overdoes being done in the ICU was eradicated after a detail study. The levels of the paracetamol were assessed with the help of Roche Modular PPE using the acetaminophen assay kit K8001, K8002,6 which is famous for its good intra and interessay accuracy. It is a well known fact the increased level of lipids can obstruct with this assay. For this situation, the patient’s lipid profile was in normal range.
Hochadel, M. (2014). Mosby's Drug Reference for Health Care Professionals (fourth edition ed.). : Elsevier.
With regards to making an orally administered drug, permeability and solubility are two key factors that affect the rate and absorption that is accomplished in the body. Permeability of a compound, is the process accomplished in the GI tract by absorption, usually in a specific segment or when exposed to certain active transporters. Solubility on the other hand, controls the rate that the drug is absorbed and control this by the different characteristics of the compound like salts, polymorphs, smaller particles and the pH.
The purpose of this experiment was to test for quality control and analysis of a commercial product, in this case vinegar. The experiment performed determined the actual molarity of a specific brand of vinegar as compared to information provided on the bottle. The standardization of HCl and NaOH was also performed in order to understand the process of titrations. The importance of testing for quality control to be sure the product being sold holds up to its commercial value and is authentic in what it advertises to be. Quality control is a way to test the standards of a commercial product by testing a sample of the output against original specifications. Quality control is also used to protect public health and ensure the safety
Precision of a patient’s intravenous medication is essential; it must be safe from. contamination, toxicity, and side effects. Most people believe these medications are compounded or mixed by a trained and licensed individual. However, this is inaccurate because the pharmacy technician actually compounds a large percentage of a patient’s medications. Compounding involves a technician’s math skills, aseptic technique, and professional ethics.... ...
Hamilton, R. (2013). Tarascon pharmacopoeia: 2013 Professional desk reference edition (p. 328). Burlington, MA: Jones and Bartlett Learning.
The conical vial was placed in a small beaker and allowed to cool to room temperature. The mixture was Cooled thoroughly in an ice bath for 15-20 minutes and crystals collected by vacuum filtration on a Hirsch funnel. The vial was rinsed with about 5 mL of ice water and transferred into to the Hirsch funnel and again washed with two additional 5mL portions of ice water. Crystals were dried for 5-10 minutes by allowing air to be drawn through them while they remained on the Hirsch funnel. The product was transferred to a watch glass plate and allow the crystals to dry in air. Crude acetaminophen product was weighed and set aside a small sample for a melting point determination and a color comparison after the next step. Calculation of the percentage yield of crude acetaminophen (MW = 151.2). was done and recorded in the lab notebook.
Vallerand, A.H., Sanoski, C.A., & Deglin, J.H. (2013). Davis’s Drug Guide for Nurses. (13th ed). Philadelphia, PA: F.A
Analysis of Aspirin Tablets Aim --- To discover the percentage of acetylsalicylic acid in a sample of aspirin tablets. ----------------------------------------------------------------- In order to do this, the amount of moles that react with the sodium hydroxide must be known. This is achieved by using the method of back titration.
HPLC (High Performance Liquid Chromatography) is an analytical technique which separates a complex mixture of components into its specific individual components. It is a powerful tool in analysis, as it combines high speed with extreme sensitivity compared to traditional methods of chromatography because of the use of a pump which creates a high pressure and forces the mobile phase to move with the analyte in high speed. It is been used as a principle technology in various automated analyzers used for diagnostic purpose.
LAB REPORT 1st Experiment done in class Introduction: Agarose gel electrophoresis separates molecules by their size, shape, and charge. Biomolecules such as DNA, RNA and proteins, are some examples. Buffered samples such as glycerol and glucose are loaded into a gel. An electrical current is placed across the gel.