Supramolecular modification of selected antitubercular drugs

Doctoral Thesis

2010

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University of Cape Town

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Abstract
The author's objective was to prepare new solid phases of the antitubercular drug isoxyl [specifically polymorphs, solvates, cyclodextrin (CD) inclusion complexes and cocrystals] and to isolate and characterise a range of solvated forms of the rifamycin antibioticsrifampicin and rifaximin.
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