Blood levels of selective antiretroviral drugs over a period of time, in Sprague-Dawley rats / Michael du Plooy
Selective antiretroviral! (ARV) drugs are primarily metabolized by cytochrome P450 (CYP) enzymes, characteristically predisposed to variation, and are therefore primarily responsible for ARV pharmacokinetic variability and associated drug interactions. For the majority of ARV drugs, the therapeutic...
Main Author: | Du Plooy, Michael |
---|---|
Published: |
North-West University
2009
|
Subjects: | |
Online Access: | http://hdl.handle.net/10394/2583 |
Similar Items
-
Blood levels of selective antiretroviral drugs over a period of time, in Sprague-Dawley rats / Michael du Plooy
by: Du Plooy, Michael
Published: (2009) -
Potential Effects of Ibuprofen, Remdesivir and Omeprazole on Dexamethasone Metabolism in Control Sprague Dawley Male Rat Liver Microsomes (Drugs Often Used Together Alongside COVID-19 Treatment)
by: Barker, J., et al.
Published: (2022) -
Potential Effects of Ibuprofen, Remdesivir and Omeprazole on Dexamethasone Metabolism in Control Sprague Dawley Male Rat Liver Microsomes (Drugs Often Used Together Alongside COVID-19 Treatment)
by: Barker, J., et al.
Published: (2022) -
Pharmacogenetics of schizophrenia in real clinical practice: a clinical case
by: R. F. Nasyrova, et al.
Published: (2018-12-01) -
Hyperlipidemia: Insights into Mechanisms Involved in Modulation of Drug Pharmacokinetics and Response
by: Marwa E. Elsherbiny
Published: (2020-03-01)