Preview

Zidovudine Case Study

Good Essays
Open Document
Open Document
1689 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Zidovudine Case Study
Objective: In the present study, an attempt was made to improve the bioavailability of Zidovudine by formulating into Orodispersible tablets, as it has poor bioavailability and extensive pre systemic metabolism.
Methods: In the present study, the mucilage extracted from Fenugreek seeds (Trigonella foenum-graecum) was used as superdisintegrant. The oral dispersible tablets were prepared by using wet granulation technique. A three factor two level (23) central composite design was employed for the optimization of formulation. The input variables chosen are amount of fenugreek mucilage, amount of mannitol, and concentration of PVP and the response parameters chosen for the optimization were Dissolution efficiency at 10 min and In-vitro dispersion
…show more content…
The prepared formulations were evaluated for different pre-compression and post-compression parameters. The In-vitro dissolution studies were carried out as per USP. The drug release profiles show that all the four optimized formulations show 100% drug release in about 20- 30 min. The actual responses such as dissolution efficiency and In-vitro dispersion time are closer to the predicted responses by design.
Conclusion: It can be concluded that the fenugreek mucilage used in the study as superdisintegrant was a good choice in making orodispersible tablets of Zidovudine and the adopted Central composite design was successful in optimizing the formulations as actual responses were comparable to that of predicted responses by design.
Key words: Zidovudine, Fenugreek mucilage, Superdisintegrant, Central composite design, Orodispersible
…show more content…
Loss on drying
1g of the sample was transferred into each of several Petri dishes and then dried in an oven at 105oC until a constant weight was obtained. The moisture content was then determined as the ratio of the weight of moisture loss to weight of sample expressed as a percentage. pH determination The pH of each of 1% suspension was measured using a pH meter to check any hydrolysis or microbial decomposition of suspensions. The change in pH is attributed to hydrolysis or microbial decomposition.
Flow properties
The flow properties of the fenugreek mucilage were studied by determining Angle of repose, carr’s compressibility index and hausner

You May Also Find These Documents Helpful

  • 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
  • Good Essays

    This experiment was based on the unknown component of “Panacetin”. In addition to our unknown, we used phenacetin, acetanilide and water. The structures of phenacetin and acetanilide are shown respectively.…

    • 1075 Words
    • 5 Pages
    Good 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
  • Satisfactory Essays

    A major hurdle that has prevented the commercialization of many promising poorly soluble drug candidates is dissolution rate-limited bioavailability or permeation rate-limited bioavailability. Buccal route of administration provides better penetration of therapeutic and diagnostic agents, and a reduced risk in comparison to conventional treatments. This leads to greater therapeutic efficacy, provides a more comfortable administration for the patient and allows preventing over dose.…

    • 305 Words
    • 2 Pages
    Satisfactory Essays
  • Good Essays

    Paw Baked Milk Lab

    • 600 Words
    • 3 Pages

    Each substance was observed inside their containers and the hypotheses were based on these observations. The volumes of each substance was then measured inside their containers. Each substance was then weighed and density calculated. After, each substance was observed under magnifying glass, smelled and touched to determine texture. Lastly, each substance was tested for solubility.…

    • 600 Words
    • 3 Pages
    Good 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
  • Satisfactory Essays

    The patient should inhale the medication rapidly. Otherwise the dry particles will stick to the…

    • 6164 Words
    • 29 Pages
    Satisfactory Essays
  • Good Essays

    Medication administration is one of the most serious activities and of greater responsibility of Nursing. In order to implement it, one should require competence, knowledge, skills and application of scientific principles as regards the preparation, the administration routes and the adverse events. This paper was aimed at performing a bibliographic review about medication administration by means of direct parenteral route, as regards the application area, the material to be used and the technique described in the literature. The methodology used was the exploratory, selective, analytical and interpretive search and reading of papers published in scientific journals by considering the intradermal, subcutaneous, intramuscular and intravenous…

    • 136 Words
    • 1 Page
    Good Essays
  • Satisfactory Essays

    Feasibility trails were carried out by melt granulation method. Method: Drug was passed from 40# sieve. Weigh accurately drug, polymer and other excipients. Wax was melted at 60-65°C.…

    • 1565 Words
    • 7 Pages
    Satisfactory Essays
  • Good Essays

    Medicated chewing gums are solid or semi-solid pharmaceutical dosage forms which contains one or more active pharmaceutical ingredients (API) and water-soluble or -insoluble excipients that is blended with a water-insoluble gum base. The drug product is intended to be chewed in the oral cavity for a specific period of time, after which the insoluble gum base is discarded. Currently available Medicated Chewing Gums (MCG) are for pain relief, smoking cessation, travel illness, and freshening of breath. Also, a large number of chewing gum intended for prevention of caries, xerostomia alleviation and vitamin/ mineral supplementation are currently available. This MCGs usually consists of a gum core, which may or may not be coated. Since the water…

    • 126 Words
    • 1 Page
    Good Essays
  • Better Essays

    Medication Administrationrsrizontal Violeneed to be considered during the time of administration. verything. Medications should always be Errors…

    • 902 Words
    • 4 Pages
    Better Essays
  • Good Essays

    Still, many medications, even those discovered with the most advanced strategies and theories, have unacceptable side effects due to the drugs interacting with parts of the body that are not intended for targeting. These side effects result in a limited ability of designing optimal medications for adverse diseases. Drug delivery systems intrigue me because they involve all aspects of medicine, engineering, chemistry, biology,…

    • 576 Words
    • 3 Pages
    Good Essays
  • Good Essays

    70 ml. of water was measured in a graduated cylinder and poured into a test tube. 7 drops of red food dye was added into the test tube. 70 ml. of water was measured in a graduated cylinder and poured into a second test tube. 7 drops of blue food dye was added into the second test tube. A piece of Lactuca sativa was placed into the red test tube so that only the stem was submerged in water. A second piece of Lactuca sativa (roughly the same size as the first) was placed into the blue test tube so that only the stem was submerged in water. The blue test tube was placed in a test tube rack in front of a fan set on low. The red test tube was placed in a test tube rack where there was no wind. After 24 hours both pieces of Lactuca sativa were taken out of the test tubes. The remaining water in the red test tube was poured into a graduated cylinder and measured. The remaining water in the blue test tube was poured into a graduated cylinder and measured.…

    • 627 Words
    • 3 Pages
    Good Essays
  • Powerful Essays

    In this study, survey based research is done. Qualitative data collection is done. The data is collected through primary research, that is, through questionnaires. The target population is the Doctors practicing in Government Hospitals, Private Clinic, and Polyclinics A sample size of 120 Doctors is taken. Purposive sampling is done. The data is analysed and then the brand preference is determined for the combination of Cefoperazone+Sulbactum in Parenteral form. The study is concluded by providing suggestions to Macleods Pharmaceuticals ltd. for improving the Brand preference of Doctors towards Zonamax injection.…

    • 9277 Words
    • 38 Pages
    Powerful Essays
  • Better Essays

    Crimazole Case Study

    • 1389 Words
    • 6 Pages

    Topical microemulsion systems for the antifungal activity containing Clotrimazole are designed to overcome the problems associated with its low solubility (0.49 mg/L) and slow dissolution in aqueous solutions. In this study, Clotrimazole was incorporated in jambhul honey microemulsion formulation without causing instability of the emulsion. The solubility of Clotrimazole in various oils, surfactants and cosurfactants was assessed to finalize the components of the w/o and o/w microemulsions. The pseudoternary diagrams were plotted to recognize the area of microemulsion region. The effect of Smix (surfactant:cosurfactant weight ratio) on the microemulsion region has been determined and optimum systems were developed. Eight Clotrimazole microemulsion formulations, each four of water/oil (isopropyl myristae/Tween 80/phophotidyl choline/water) and oil/water (oleic acid/Cremophor EL/Transcutol P/water) were prepared and evaluated. The…

    • 1389 Words
    • 6 Pages
    Better Essays