Protein-Free Efavirenz Concentrations in Cerebrospinal Fluid and Blood Plasma Are Equivalent: Applying the Law of Mass Action To Predict Protein-Free Drug Concentration

ABSTRACT Efavirenz (EFV) is one of the most commonly prescribed antiretroviral drugs (ARVs) for the treatment of HIV. Highly protein-bound drugs, like EFV, have limited central nervous system (CNS) penetration when measured using total drug concentration gradients between blood plasma (BP) and cerebrospinal fluid (CSF). However, the more relevant pharmacologically active protein-free drug concentrations are rarely assessed directly in clinical studies. Using paired BP and CSF samples obtained from 13 subjects on an EFV-containing regimen, both the protein-free and total concentrations of EFV were determined. Despite a median (interquartile range [IQR]) total EFV BP/CSF concentration ratio of 134 (116 to 198), the protein-free EFV BP/CSF concentration ratio was 1.20 (0.97 to 2.12). EFV median (IQR) protein binding was 99.78% (99.74 to 99.80%) in BP and 76.19% (74.47 to 77.15%) in CSF. In addition, using the law of mass action and an in vitro-derived EFV-human serum albumin dissociation constant, we have demonstrated that the predicted median (IQR) protein-free concentration in BP, 4.59 ng/ml (4.02 to 9.44 ng/ml), compared well to that observed in BP, 4.77 ng/ml (3.68 to 6.75 ng/ml). Similar results were also observed in CSF and seminal plasma. This method provides a useful predictive tool for estimating protein binding in varied anatomic compartments. Our results of equivalent protein-free EFV concentrations in BP and CSF do not support prior concerns of the CNS as a pharmacological sanctuary from EFV. As CSF penetration of ARVs may increase our understanding of HIV-associated neurological dysfunction and antiretroviral effect, assessment of protein-free CSF concentrations of other highly protein-bound ARVs is warranted.

[1]  Jintanat Ananworanich,et al.  Central nervous system viral invasion and inflammation during acute HIV infection. , 2012, The Journal of infectious diseases.

[2]  Michael Rayment,et al.  Prevention of HIV-1 infection with early antiretroviral therapy , 2012, Journal of Family Planning and Reproductive Health Care.

[3]  I. Grant,et al.  Low Cerebrospinal Fluid Concentrations of the Nucleotide HIV Reverse Transcriptase Inhibitor, Tenofovir , 2012, Journal of acquired immune deficiency syndromes.

[4]  U. Holzgrabe,et al.  Overton's Rule Helps To Estimate the Penetration of Anti-Infectives into Patients' Cerebrospinal Fluid , 2011, Antimicrobial Agents and Chemotherapy.

[5]  J. Baeten,et al.  Characteristics of HIV-1 Serodiscordant Couples Enrolled in a Clinical Trial of Antiretroviral Pre-Exposure Prophylaxis for HIV-1 Prevention , 2011, PloS one.

[6]  C. Hendrix,et al.  The Male Genital Tract Is Not a Pharmacological Sanctuary From Efavirenz , 2011, Clinical pharmacology and therapeutics.

[7]  R. Haubrich,et al.  Efavirenz concentrations in CSF exceed IC50 for wild-type HIV. , 2011, The Journal of antimicrobial chemotherapy.

[8]  David V Glidden,et al.  Preexposure chemoprophylaxis for HIV prevention in men who have sex with men. , 2010, The New England journal of medicine.

[9]  D. Meyers,et al.  A highly sensitive ultra performance liquid chromatography-tandem mass spectrometric (UPLC-MS/MS) technique for quantitation of protein free and bound efavirenz (EFV) in human seminal and blood plasma. , 2010, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[10]  Edward H. Kerns,et al.  The effect of plasma protein binding on in vivo efficacy: misconceptions in drug discovery , 2010, Nature Reviews Drug Discovery.

[11]  F. Sörgel,et al.  Penetration of Drugs through the Blood-Cerebrospinal Fluid/Blood-Brain Barrier for Treatment of Central Nervous System Infections , 2010, Clinical Microbiology Reviews.

[12]  Lynn Morris,et al.  Effectiveness and Safety of Tenofovir Gel, an Antiretroviral Microbicide, for the Prevention of HIV Infection in Women , 2010, Science.

[13]  Amalio Telenti,et al.  Antiretroviral Treatment of Adult HIV Infection2010 Recommendations of the International AIDS Society–USA Panel , 2010 .

[14]  S. Broder,et al.  The development of antiretroviral therapy and its impact on the HIV-1/AIDS pandemic. , 2010, Antiviral research.

[15]  I. Grant,et al.  Low atazanavir concentrations in cerebrospinal fluid , 2009, AIDS.

[16]  Peter Reiss,et al.  Antiretroviral treatment of adult HIV infection: 2008 recommendations of the International AIDS Society-USA panel. , 2008, JAMA.

[17]  B. Caffo,et al.  Effect of Semen Sampling Frequency on Seminal Antiretroviral Drug Concentration , 2008, Clinical pharmacology and therapeutics.

[18]  K. Korzekwa,et al.  Impact of pH on plasma protein binding in equilibrium dialysis. , 2008, Molecular pharmaceutics.

[19]  B. Brew,et al.  Biomarkers of HIV related central nervous system disease , 2008, International review of psychiatry.

[20]  I. Grant,et al.  Validation of the CNS Penetration-Effectiveness rank for quantifying antiretroviral penetration into the central nervous system. , 2008, Archives of neurology.

[21]  Douglas D. Richman,et al.  Antiretroviral Treatment of Adult HIV Infection , 2008 .

[22]  R. Ellis,et al.  Lopinavir concentrations in cerebrospinal fluid exceed the 50% inhibitory concentration for HIV , 2005, AIDS.

[23]  J. McArthur HIV dementia: an evolving disease , 2004, Journal of Neuroimmunology.

[24]  K. Marder,et al.  Attenuated central nervous system infection in advanced HIV/AIDS with combination antiretroviral therapy. , 2004, Archives of neurology.

[25]  C. Petropoulos,et al.  Natural Variation of Drug Susceptibility in Wild-Type Human Immunodeficiency Virus Type 1 , 2004, Antimicrobial Agents and Chemotherapy.

[26]  V. Miller,et al.  Protein binding in antiretroviral therapies. , 2003, AIDS research and human retroviruses.

[27]  A. Fura,et al.  Shift in pH of biological fluids during storage and processing: effect on bioanalysis. , 2003, Journal of pharmaceutical and biomedical analysis.

[28]  N. Sacktor The epidemiology of human immunodeficiency virus-associated neurological disease in the era of highly active antiretroviral therapy. , 2002, Journal of neurovirology.

[29]  D I Stuart,et al.  Structural basis for the resilience of efavirenz (DMP-266) to drug resistance mutations in HIV-1 reverse transcriptase. , 2000, Structure.

[30]  K. Tashima,et al.  Cerebrospinal fluid human immunodeficiency virus type 1 (HIV-1) suppression and efavirenz drug concentrations in HIV-1-infected patients receiving combination therapy. , 1999, The Journal of infectious diseases.

[31]  K. P. Murphy,et al.  Evaluation of linked protonation effects in protein binding reactions using isothermal titration calorimetry. , 1996, Biophysical journal.

[32]  C. Petito,et al.  Blood‐brain barrier abnormalities in acquired immunodeficiency syndrome: Immunohistochemical localization of serum proteins in postmortem brain , 1992, Annals of neurology.

[33]  R. Rhodes Evidence of Serum-Protein Leakage Across the Blood-Brain Barrier in the Acquired Immunodeficiency Syndrome , 1991, Journal of neuropathology and experimental neurology.

[34]  L. Resnick,et al.  Early penetration of the blood‐brain‐barrier by HIV , 1988, Neurology.

[35]  I. Elovaara,et al.  CSF protein and cellular profiles in various stages of HIV infection related to neurological manifestations , 1987, Journal of the Neurological Sciences.