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    The effect of native cassava starch on the disintegration of formulated paracetamol tablets

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    Date
    2010
    Author
    Kamau, JM
    Type
    Thesis; en_US
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    Abstract
    The project involved the use of extracted cassava starch from raw cassava tubers as a disintegrant in the manufacture of tablets. However, there was also manufacture of tablets using industrial corn starch. The tablets obtained were tested for comparison. Other physicochemical tests were conducted on the locally acquired cassava starch. The extracted cassava starch was also subjected to tests such as solubility, cyanogenic glycoside, iodine, tannin, angle of repose, bulk density, swelling capacity, and moisture content. The starch was confirmed and found to be insoluble in water and ethanol, cyanogenic glycosides were present, no tannins were present and bulk density, swelling capacity and moisture content results were recorded accordingly. Wet granulation was then done to make granules that would be used to make the tablets. Small granules were then formed by passing them through different SIeves viz:710um,500um,355um,250um,180um,125um.The granules weights were then recorded and results tabulated. The granules were then used to make corn and cassava tablets for comparison tests. The comparison of the tablets formed by the cassava and corn starches was then done in the form of different tests done viz; disintegration, mechanical strength, friability, hardness and uniformity of weight. This tests were done following relevant Standard Operating Procedures as they were stipulated. The use of locally acquired starches such as cassava was a noble approach however the rates of disintegration, friability, mechanical strength and other tests done on the tablets showed corn starch was the preferred disintegrant and that it was the disintegrant of choice as it served as a staple food for the country thus its availability. A risk of using cassava was evident due to it containing cyanogenic glycosides as evidenced by the test. The tablets seemed not to pass friability and disintegration tests as the compression was not adequate during tableting.Most tablets passed the uniformity of weight test.Deviations from the mean weight were presented in table format.
    URI
    http://hdl.handle.net/11295/74498
    Citation
    A dissertation submitted in partial fulfillment of the requirements for the award of the degree of bachelor of pharmacy of the University of Nairobi.
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    • Faculty of Health Sciences (FHS) [4559]

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