Search Results - "BACK, D. J"
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Comparison of the induction profile for drug disposition proteins by typical nuclear receptor activators in human hepatic and intestinal cells
Published in British journal of pharmacology (01-02-2008)“…Background and purpose: Certain nuclear receptors (NRs) such as the constitutive androstane receptor (CAR), pregnane X receptor (PXR) and farnesoid X receptor…”
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The impact of cytokines on the expression of drug transporters, cytochrome P450 enzymes and chemokine receptors in human PBMC
Published in British journal of pharmacology (01-02-2009)“…Mandarin translation of Background and purpose: The function of transporters in peripheral blood mononuclear cells (PBMC) has been characterized, but less is…”
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The intracellular pharmacology of antiretroviral protease inhibitors
Published in Journal of antimicrobial chemotherapy (01-12-2004)“…Therapeutic drug monitoring (TDM) of antiretroviral protease inhibitors (PIs) has been suggested to have the potential to both reduce toxicity and optimize…”
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Improved Oral Bioavailability of Lopinavir in Melt-Extruded Tablet Formulation Reduces Impact of Third Trimester on Lopinavir Plasma Concentrations
Published in Antimicrobial Agents and Chemotherapy (01-02-2012)“…Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
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5
The Effect of Gene Variants on Levonorgestrel Pharmacokinetics When Combined With Antiretroviral Therapy Containing Efavirenz or Nevirapine
Published in Clinical pharmacology and therapeutics (01-09-2017)“…Reduced levonorgestrel concentrations from the levonorgestrel contraceptive implant was previously seen when given concomitantly with efavirenz. We sought to…”
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Cultured CD4T cells and primary human lymphocytes express hOATPs: intracellular accumulation of saquinavir and lopinavir
Published in British journal of pharmacology (01-11-2008)“…Background and purpose: Drug efflux tranporters (P‐glycoprotein (P‐gp), multidrug resistance‐associated protein (MRP)) limit the cellular uptake of human…”
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A Call for a Consortium for Optimal Management of Drug–Drug Interactions in Patient Care
Published in Clinical pharmacology and therapeutics (01-09-2017)“…During clinical development of medicines, manufacturers are obliged to assess the risk of drug–drug interactions (DDIs) with their new drug. There is no doubt…”
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Differential inhibition of cytochrome P450 isoforms by the protease inhibitors, ritonavir, saquinavir and indinavir
Published in British journal of clinical pharmacology (01-08-1997)“…Aims To compare the inhibitory potential of the HIV protease inhibitors saquinavir, ritonavir and indinavir against CYP1A2, CYP2C9, CYP2E1 and CYP3A4 catalysed…”
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P-glycoprotein and MRP1 expression and reduced ritonavir and saquinavir accumulation in HIV-infected individuals
Published in Journal of antimicrobial chemotherapy (01-10-2002)“…Objectives: Efflux transporters may play a role in lowering intracellular drug concentrations. As the HIV protease inhibitors are substrates for the efflux…”
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10
A longitudinal study of maternal dose response to low molecular weight heparin in pregnancy
Published in Obstetrics and gynecology (New York. 1953) (01-06-2003)“…To assess the maternal response to low molecular weight heparin during pregnancy, by estimation of plasma anti-Xa activity, at three specified gestation points…”
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Therapeutic drug monitoring of atazanavir/ritonavir in pregnancy
Published in HIV medicine (01-11-2014)“…Objectives Pregnant women experience physiological changes during pregnancy that can have a significant impact on antiretroviral pharmacokinetics. Ensuring…”
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The impact of pharmacogenetics on HIV therapy
Published in International journal of STD & AIDS (01-03-2009)“…The use of highly active antiretroviral therapy in the treatment of HIV infection has resulted in significant reductions in mortality and morbidity worldwide…”
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Therapeutic drug monitoring of lopinavir/ritonavir in pregnancy
Published in HIV medicine (01-03-2011)“…Objectives The aim of the study was to determine total and unbound lopinavir (LPV) plasma concentrations in HIV‐infected pregnant women receiving…”
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15
Differential selectivity of cytochrome P450 inhibitors against probe substrates in human and rat liver microsomes
Published in British journal of clinical pharmacology (01-02-1998)“…Aims Chemical inhibitors of cytochrome P450 (CYP) are a useful tool in defining the role of individual CYPs involved in drug metabolism. The aim of the…”
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A Compartmental Pharmacokinetic Evaluation of Long-Acting Rilpivirine in HIV-Negative Volunteers for Pre-Exposure Prophylaxis
Published in Clinical pharmacology and therapeutics (01-09-2014)“…Rilpivirine long‐acting (RPV‐LA) is a parenteral formulation enabling prolonged plasma exposure. We explored its multiple‐compartment pharmacokinetics (PK)…”
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Modulation of P-glycoprotein function in human lymphocytes and Caco-2 cell monolayers by HIV-1 protease inhibitors
Published in AIDS (London) (10-09-1999)“…To determine the effect of the protease inhibitors ritonavir, nelfinavir and indinavir on the P-glycoprotein (P-gp)-mediated transport of saquinavir in Caco-2…”
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Effects of drugs on 2',3'-dideoxy-2',3'-didehydrothymidine phosphorylation in vitro
Published in Antimicrobial Agents and Chemotherapy (01-06-1997)“…Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon…”
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Detection of ABCC2, CYP2B6 and CYP3A4 in human peripheral blood mononuclear cells using flow cytometry
Published in Journal of immunological methods (31-12-2008)“…ABCC2 has a wide tissue distribution and can mediate the efflux of a number of therapeutic compounds from cells and contribute to potential treatment failure…”
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The Relationships of ABCB1 3435C>T and CYP2B6 516G>T With High-Density Lipoprotein Cholesterol in HIV-Infected Patients Receiving Efavirenz
Published in Clinical pharmacology and therapeutics (01-08-2009)“…Non‐nucleoside reverse transcriptase inhibitors (NNRTIs) are associated with a favorable increase in high‐density lipoprotein cholesterol (HDL‐c) level…”
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