Preview

Variables Affecting The Dissolution Profile Of Zolmitripna F13 Answers

Powerful Essays
Open Document
Open Document
983 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Variables Affecting The Dissolution Profile Of Zolmitripna F13 Answers
Variables Affecting the Dissolution Profile of Zolmitriptan Liquisolid OrodispersibleTablets(ODTs)
Different formulas were prepared (F1-F18) using different variables to reach the best formula. Each formula was evaluated to study the pre and post compression parameters. Angle of repose, carr's index and Hausner's ratio as a pre-compression tests for powder flow properties as well as hardness, friability, wetting time, content uniformity and in vitro disintegration time as a post-compression tests for tablet physical properties.
2.3.9.1 Effect of Superdisintegrants Types and Concentrations
The effect of different types and concentrations of the superdisintegrants on the physical properties of Zolmitriptan liquisolid orodispersible tablets
…show more content…
This loading factor was decreased to 50% in formula F17 to become 0.175. Formula F18 the loading factor 0.25 was decreased to 100% to become 0.125 .This change in the loading factor was done to study the effect on the physical properties and dissolution behavior of the prepared ODTs of Zolmitriptan.
2.3.10 In Vivo Disintegration Test for the Selected Formula
The time necessary for determination of disintegration time in the oral cavity was calculated from 6 healthy volunteers. All volunteers were told about the purpose of the test. Before performing the test, the mouth cavity was washed with water. The tablet was positioned on the tongue and after that the tongue was quietly moved. The time needed for the elimination of any fragment of the tablet was measured with a stopwatch and recorded as a disintegration time (DT) (97).
2.3.11In vivo pharmacokinetic study in healthy human volunteers
2.3.11.1Study

You May Also Find These Documents Helpful

  • Powerful Essays

    Sodium saccharin (0.446 g) was dissolved in N-N-dimethylformamide (DMF) at 80oC. Iodoethane (0.16 mL) was added and heated at constant temperature (80oC) for ten minutes. The product was separated by adding water to the room temperature solution, further cooled in ice and the solid collected and dried via vacuum filtration. The following week, the dried product (0.442g) was analyzed by melting point (87.8-94.7oC), and a 1H NMR spectrum.…

    • 954 Words
    • 4 Pages
    Powerful Essays
  • Good Essays

    0.30093 g of panacetin was weighed and mixed well with 50 ml of dichloromethane. After stirring the solution thoroughly, some solid is formed (solid sucrose) and liquid. With using a preweighed filter paper to filter the mixture, and after the sucrose had dried, it was weighed out to 0.7756g. For the aqueous layer, adding 10ml of 6M HCl(pH 2) and filtered using vacuum filtration and after cooled in the ice bath. Leaving behind is the solid aspirin which was weighed out as 1.2469g. Lastly, to measure the weight of the unknown solid component of panacetin, putting the organic layer in a warm water bath to evaporate the solvent and the remain is the solid residue. Extract the unknown solid component of panacetin, which was weighed to be 0.8946g.…

    • 674 Words
    • 3 Pages
    Good Essays
  • Powerful Essays

    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 isolated aspirin.…

    • 1653 Words
    • 7 Pages
    Powerful Essays
  • Satisfactory Essays

    In this lab the results were recorded in two sections separated in sucrose and aspirin. The sucrose results were recorded as being in a solid state, having a white color and having a weighed mass of .21 grams. The aspirin results were recorded as a solid state, having a white color and having a weighed a mass of .10…

    • 479 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    The purpose of this experiment is to investigate the composition of a simulated pharmaceutical preparation Panacetin, a proposed type of pain-killer. Panacetin is typically made up of sucrose, aspirin, and acetaminophen, but the third component in this experiment is unknown. The unknown component is suspected to be a chemical relative of acetaminophen, either acetanilide or phenacetin. Using techniques such as extraction, evaporation, and filtration, the three components will be isolated based on their solubilities and acid-base properties. The percent composition of Panacetin will also be deduced based on the masses of the three dried components; this is done to verify the composition attained is consistent with those listed on the preparations label. As a result of this investigation, my teammates and I allowed the Panacetin to undergo gravity filtration and separation techniques in order to identify whether there are any discrepancies in the components of the Panacetin. Furthermore, recrystallization and purification methods were used to determine if the unknown substance were similar in properties to either of the suspected unknown substances by comparing factors such as melting points to the chemical properties of phenactin and acetanilide. The results were as expected, based on the molecular weights and ratios of each separated chemicals, as well as the boiling point of the unknown it was determined that these ranges were close enough to indicate that the label is reasonably accurate in its composition. To add on however the identity of the unknown component differed from what the label indicated. In the end, the percentage composition attained based on our observations and yield confirmed that indeed the chemical composition of Panacetin were as indicated on the preparations label. The identity of the unknown component however suggested that the preparation did not contain acetaminophen as indicated, but instead was consistent with the chemical properties…

    • 305 Words
    • 2 Pages
    Good Essays
  • Better Essays

    Redox Area Lab Report

    • 741 Words
    • 3 Pages

    1. The appearance and solubility compares well with the information presented from the CRC Handbook. Our test results shows that…

    • 741 Words
    • 3 Pages
    Better Essays
  • Good Essays

    Pre-Lab: Analgesic drugs are known for reducing pain, while antiseptic drugs reduce symptoms such as fevers and swelling. However, some of these drugs can reduce both illnesses. To obtain a pure compound in these drugs, the scientist needs to separate the desired compound by taking advantage of the different physical and chemical properties. Such as; different boiling points, melting points and their solubility properties. To do this a chemist can also asses the differences between acidic and basic substances when they are added to water soluble mixtures. Within this current experiment I will asses the pharmaceutical preparation of Panacetin, by using it 's solubility along with other organic molecules. We know that Panacetin is made up of sucrose, aspirin and some other unknown substance. We know the substance has to be Phenacetin or Acetanilide. To help solidify our reasoning, we need a % recovery of 8-12% sucrose, 35-45% aspirin and 45-55% unknown.…

    • 1948 Words
    • 56 Pages
    Good Essays
  • Better Essays

    To be able to understand how organic soluble compounds could be isolated from non-organic components, a chromatographic separation process was used. The objective of the analgesic drug identification is to isolate the organic compounds/ active ingredients in an unknown drug. The identity of the drug was determined through melting point, percent recover, and Rf values. The comparable data for acetaminophen from the manufacturer is 500mg of active ingredient. After conducting the experiment-extraction, distillation, and evaporation- 451mg of active ingredient. This relates to a 68.1% recovery. The melting point was between 158 and 165 degrees Celsius, which is almost ten degrees lower than the published melting point of acetaminophen. After conducting a TLC plate, the Rf value was calculated to be .4268, the same as the standard Rf.…

    • 1180 Words
    • 4 Pages
    Better Essays
  • Good Essays

    Tlc questions

    • 567 Words
    • 3 Pages

    8. A 50/50 mixture of dichloromethane and ethanol was added to the crushed analgesic tablets to fully dissolve the tablets because the whole tablet will not dissolve as it contained not only the analgesic, but also binders, buffering agents and other components that would not make the tablet to fully dissolve in just a polar solvent.…

    • 567 Words
    • 3 Pages
    Good Essays
  • Better Essays

    In this experiment, several analgesics were analyzed by Thin Layer Chromatography (TLC) and the composition of an unknown tablet was identified. We define chromatography as the separation of two or more compounds or ions by their molecular interactions by either a moving or a stationary phase.1 There are different types of chromatography: Thin Layer Chromatography (TLC), Gas Liquid Chromatography (GC), and Column Chromatography (CC). All of which there two phases: mobile and stationary. Phases can be a solid and a liquid, a liquid and a liquid, a gas and a solid, or a gas and a liquid. The stationary phase is also known as the absorbent. Greater affinity, or attraction, for the mobile phases will move faster and conversely for stationary phases.2 Running a solvent past the absorbent complex in order to remove analytes from the absorbent is known as elution. This process aids in determining affinity.3 The most polar compound is always the absorbent; however, the polarity of the compounds in the mixture in addition to the solvents found in the mixture differs in polarities.…

    • 842 Words
    • 4 Pages
    Better Essays
  • Satisfactory Essays

    Alka Seltzer Experiment

    • 165 Words
    • 1 Page

    After the experiment, I thought and considered that my hypothesis was correct. It had been that the half crushed tablet had dissolved much faster then the other types of tablet. By increasing the surface area the reaction rate of the tablet will dissolve much faster.…

    • 165 Words
    • 1 Page
    Satisfactory Essays
  • Good Essays

    The product was placed in a beaker, and enough aqueous methylated spirit (IMS) was added whilst the mixture was heated to dissolve the product. The mixture was then left to cool and was placed in ice to aid crystallization. The product was vacuum filtrated after a few minutes of standing in ice and the crystals were collected and dried in a vacuum oven at 40 degrees celsius. The mass of the crystals was calculated and the melting point was determined.…

    • 652 Words
    • 3 Pages
    Good Essays
  • Good Essays

    SoluTab= Dissolves in water or on the tongue in less than 1 minute. When on the tongue, swallow the remenints…

    • 948 Words
    • 5 Pages
    Good Essays
  • Good Essays

    Thin Layer Chromatography

    • 564 Words
    • 3 Pages

    The behavior of these compounds in function of their structure and polarity were inversely associated. The TLC plate is made up of highly polar silica gel. Caffeine showed the smallest Rf value of (.278), shadowed by acetaminophen Rf value of .5556 cm, followed by acetylsalicylic acid’s Rf value of (.667), and then the largest Rf value that ibuprofen had of (.722). The polar molecules of the analgesic drugs were attracted to the highly polar silica gel, which explains the low retention rate of caffeine that and the high retention rate of the ibuprofen that is the least non-polar.…

    • 564 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Liquid-vapor phase of acetone/chloroform was studied through distilling a series of mixtures with different mole fraction. When the mixtures were boiling, their vapor was condensed through a water column and collected in a receiving container. Refractive index was collected for starting mixture, distillate and residue for each sample. A boiling temperature versus acetone’s mole fraction was constructed to show the liquid-vapor phase diagram. The boiling temperature of azeotrope was determined to be 62.2oC with the composition of 23% acetone and 77% chloroform.…

    • 1345 Words
    • 6 Pages
    Good Essays

Related Topics