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dc.contributor.advisorSamsodien, Halima
dc.contributor.authorNgilirabanga, Jean Baptiste
dc.date.accessioned2021-08-16T09:15:50Z
dc.date.available2021-08-16T09:15:50Z
dc.date.issued2021
dc.identifier.urihttp://hdl.handle.net/11394/8332
dc.descriptionDoctor Pharmaceuticae - DPharmen_US
dc.description.abstractTreatment of the human immunodeficiency virus (HIV) and tuberculosis (TB) infections have become very complicated due to the advent of drug resistance. Drug combinations offer an alternative approach to reducing the emergence of drug resistance. Pharmaceutical co-crystals have provided the pharmaceutical industry with the ability to optimise the physicochemical properties of active pharmaceutical ingredients (APIs) while preserving the biological activity. Pharmaceutical co-crystals are formed between APIs and suitable co-formers that are biologically safe or even a second or third API.en_US
dc.language.isoenen_US
dc.publisherUniversity of Western Capeen_US
dc.subjectHIV/AIDSen_US
dc.subjectTuberculosisen_US
dc.subjectInfectious diseasesen_US
dc.subjectDrug resistanceen_US
dc.subjectSolid dispersionsen_US
dc.titleSelected antiretroviral and anti-tuberculosis drug combinations by non-covalent bondingen_US
dc.rights.holderUniversity of Western Capeen_US


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