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Showing 1 to 20 of 124 for “"Drug interactions"”.

  1. Drug-drug interactions between antiretrovirals and bedaquiline

    … for multiple reasons, including potential drug-interactions. Drug-resistant TB is difficult to treat and is associated with high treatment failure rates, mainly because the antimycobacterial drugs currently available are ineffective against drug-resistant TB. Bedaquiline is a new …

    cape-town Repository record for Drug-drug interactions between antiretrovirals and bedaquiline (opens in a new tab)

  2. Predicting drug interactions with a three level causal model

    … for predicting qualitative pharmacodynamic interactions of the cardiovascular system is described. TLCM traces causal paths of drug action through up to three levels of drug action. The three levels which are molecular/receptor level, physiological level and clinical level provide both deep …

    vt Repository record for Predicting drug interactions with a three level causal model (opens in a new tab)

  3. Mathematical modelling of host-disease-drug interactions in HIV disease

    … that the virus exhibits by the accumulation of drug-resistant mutations in its genome. Current therapeutic strategies aim at achieving and maintaining a low viral burden and typically involve multiple drugs. The choice of optimal combinations of these drugs is crucial, particularly in the …

    potsdam-diss Repository record for Mathematical modelling of host-disease-drug interactions in HIV disease (opens in a new tab)

  4. Renal Drug Transporters – Clinical Significance and Role in Drug-Drug Interactions

    Drug transporters play an important role in drug disposition and can be major determinants of drug pharmacokinetics, pharmacodynamics and toxicity. In contrast to drug metabolizing enzymes, which mainly concentrate in the liver and small intestine, drug transporters are expressed ubiquitously …

    washington Repository record for Renal Drug Transporters – Clinical Significance and Role in Drug-Drug Interactions (opens in a new tab)

  5. FEXOFENADINE AND ORGANIC ANION TRANSPORTING POLYPEPTIDES (OATPs): TRANSPORT AND DRUG-DRUG INTERACTIONS

    … and disposition of fexofenadine, suggesting this drug could be used as a probe of transporter activity. When fexofenadine was administered in combination with four drugs (buspirone, caffeine, dextromethorphan and losartan) used to probe cytochrome P450 (CYP) activities, a significant decrease in …

    ku Repository record for FEXOFENADINE AND ORGANIC ANION TRANSPORTING POLYPEPTIDES (OATPs): TRANSPORT AND DRUG-DRUG INTERACTIONS (opens in a new tab)

  6. Role of Membrane Transporters in Drug Delivery, Drug Disposition And Drug-Drug Interactions

    … membrane transporters which play a vital role in drug absorption, distribution, metabolism and excretion. Understanding of functionality and molecular expression of drug transporters can prove to be of utmost importance in drug delivery or drug design by targeting specific transporter proteins. …

    umkc Repository record for Role of Membrane Transporters in Drug Delivery, Drug Disposition And Drug-Drug Interactions (opens in a new tab)

  7. Effect of berberine on in vitro metabolism of sulfonylureas: a herb-drug interactions study

    … to control their blood glucose. Potential interactions at uptake of compounds through P-gp, a 170 kDa ATP-dependent glycoprotein and drug transporter can affect their absorption. Furthermore, competitive binding at the catalytic sites of metabolic enzymes of drug and herb may mutually …

    middlesex

  8. Nonlinear mixed-effects modelling of drug-drug interactions between antiretroviral therapy and tuberculosis treatment

    … treatment of HIV and TB often results in drug-drug interactions (DDIs), mediated especially by rifampicin, a key component of the TB regimen and potent enzyme and transporter inducer. These DDIs may compromise treatment safety and efficacy, potentially leading to therapeutic failure and …

    cape-town Repository record for Nonlinear mixed-effects modelling of drug-drug interactions between antiretroviral therapy and tuberculosis treatment (opens in a new tab)

  9. Quantitative Structure-Activity Relationship Modeling to Predict Drug-Drug Interactions Between Acetaminophen and Ingredients in Energy Drinks

    The evaluation of drug-drug interactions (DDI) is a crucial step in pharmaceutical drug discovery and design. Unfortunately, if adverse effects are to occur between the co-administration of two or more drugs, they are often difficult to test for. Traditional methods rely on in vitro studies as a …

    queens Repository record for Quantitative Structure-Activity Relationship Modeling to Predict Drug-Drug Interactions Between Acetaminophen and Ingredients in Energy Drinks (opens in a new tab)

  10. Pharmacometrics of dolutegravir and tenofovir: a quantitative approach to characterise drug-drug interactions, pharmacogenetics and optimise treatment

    … often challenging because of the potential for drug-drug interactions. Dolutegravir-based regimens are now the preferred first-line option for the management of HIV. Therefore, many African countries have transitioned most PLWH from efavirenz- to dolutegravir-based regimens. A fixed-dose …

    cape-town Repository record for Pharmacometrics of dolutegravir and tenofovir: a quantitative approach to characterise drug-drug interactions, pharmacogenetics and optimise treatment (opens in a new tab)

  11. Pharmacometric modelling to inform and improve TB and HIV treatment: Focus on drug-drug interactions and neglected populations

    … those with co-morbidities requiring additional drug treatments, and those with drug-resistant strains. This leaves many unanswered questions surrounding the management of TB, HIV, and TB/HIV in these vulnerable subpopulations. In this thesis, we utilise population pharmacokinetics and …

    cape-town Repository record for Pharmacometric modelling to inform and improve TB and HIV treatment: Focus on drug-drug interactions and neglected populations (opens in a new tab)

  12. Development of a TSM Biosensor for the Determination of DNA- Drug Interactions: A Novel Method to Assist Drug Development

    … and kinetics of binding of chemotherapeutic drugs to DNA are generally time consuming and/or expensive. Moreoxer. a combination of approaches is required if both the mechanism and the kinetics of binding are to he determined, e.g. LJV spectroscopy can be used to determine the kinetics of …

    de-montfort Repository record for Development of a TSM Biosensor for the Determination of DNA- Drug Interactions: A Novel Method to Assist Drug Development (opens in a new tab)

  13. Vitamin D Levels Affect Survival in a BCR-ABL Acute Lymphoblastic Leukemia Mouse Model but Do Not Cause Vitamin-Drug Interactions

    … inducers or inhibitors if co-administered with drugs that are CYP3A4 substrates lead to marked drug-drug interactions. Because vitamin D is known to regulate intestinal CYP3A expression and gut CYP3A expression plays an important role in pre-systemic metabolism of CYP3A drugs, we determined the …

    tenn-hsc Repository record for Vitamin D Levels Affect Survival in a BCR-ABL Acute Lymphoblastic Leukemia Mouse Model but Do Not Cause Vitamin-Drug Interactions (opens in a new tab)

  14. Improvement of Gastroparesis Management By Addressing Challenges in Drug Metabolism: Studies with Metabolite Identification, Reaction Phenotyping and In Vitro Drug-Drug Interactions

    … will ensure safe and effective use of these drugs and hence enhance the clinical outcome. The thesis starts with an introductory chapter which comprises a comprehensive literature review on gastroparesis and the available pharmacological treatment options. The chapter also emphasizes the …

    temple Repository record for Improvement of Gastroparesis Management By Addressing Challenges in Drug Metabolism: Studies with Metabolite Identification, Reaction Phenotyping and In Vitro Drug-Drug Interactions (opens in a new tab)

  15. EXPANDING THE TOOLKIT: STRUCTURE, DYNAMICS, AND DRUG INTERACTIONS OF THE “PRIMING LOOP” FROM HEPATITIS B VIRUS PRE-GENOMIC RNA BY SOLUTION NMR SPECTROSCOPY

    … can probe the structure, dynamics, and interactions of RNA in solution at atomic resolution, opening the door to their functional understanding. However, NMR analysis of RNA – with only four unique ribonucleotide building blocks – suffers from spectral crowding and broad linewidths, …

    maryland Repository record for EXPANDING THE TOOLKIT: STRUCTURE, DYNAMICS, AND DRUG INTERACTIONS OF THE “PRIMING LOOP” FROM HEPATITIS B VIRUS PRE-GENOMIC RNA BY SOLUTION NMR SPECTROSCOPY (opens in a new tab)

  16. Population pharmacokinetic models describing drug-drug interactions and variability in HIV infected South Africans on protease inhibitor-based antiretroviral regimens with and without tuberculosis

    … reduced adherence leads to the development of drug resistance. The projects in this thesis were designed to characterize the population pharmacokinetic parameters of lopinavir and ritonavir in HIV infected South Africans, to account for the drug-drug interactions between lopinavir, ritonavir …

    cape-town Repository record for Population pharmacokinetic models describing drug-drug interactions and variability in HIV infected South Africans on protease inhibitor-based antiretroviral regimens with and without tuberculosis (opens in a new tab)

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