TY - JOUR
T1 - Distribution of ganciclovir in the porcine central nervous system
AU - Guldbæk, Johan Mikkel
AU - Mariager, Theis
AU - Nielsen, Mikkel Dreyer
AU - Terkelsen, Jacob Holmen
AU - Nau, Roland
AU - Bjarkam, Carsten Reidies
AU - Nielsen, Henrik
AU - Bodilsen, Jacob
PY - 2025/5/7
Y1 - 2025/5/7
N2 - Ganciclovir is often used compassionately for encephalitis due to cytomegalovirus (CMV) and human herpes virus 6b (HHV-6b). Ganciclovir pharmacokinetic studies in the central nervous system (CNS) generally rely on single measurements in the cerebrospinal fluid (CSF) or homogenized brain tissue. Therefore the objective was to compare brain extracellular fluid (ECF) concentrations of ganciclovir with plasma and CSF concentrations in a porcine model, using microdialysis during a 24 h period. Six Danish landrace pigs (female, age 4 months, 31-37 kg) received two weight-adjusted intravenous doses of ganciclovir. Unbound ganciclovir concentrations were determined by microdialysis over 24 h in five compartments: CSF (lateral ventricle, cisterna magna, and lumbar) and brain ECF (cortical and subcortical). Data were compared with paired plasma samples. Ganciclovir concentrations >IC
50 for CMV (1.6 µg/mL) were achieved in all compartments. Concentrations >IC
90 for CMV (8.3 µg/mL) were only achieved in plasma and the lumbar CSF compartment. The concentration time curves indicated higher lumbar and cisternal CSF concentrations than ECF concentrations. The ECF compartments achieved greater maximum concentration (C
max), area under the concentration time curve (AUC), and time >IC
50 after the second dose, and an accumulation ratio (R
ac) >1. The greater C
max, AUC, time >IC
50, and R
ac >1 in the ECF compartments with repeated dosages suggest that therapeutic concentrations may be achieved during long-term treatment. A higher loading dose might be warranted to improve early viral inhibition.
AB - Ganciclovir is often used compassionately for encephalitis due to cytomegalovirus (CMV) and human herpes virus 6b (HHV-6b). Ganciclovir pharmacokinetic studies in the central nervous system (CNS) generally rely on single measurements in the cerebrospinal fluid (CSF) or homogenized brain tissue. Therefore the objective was to compare brain extracellular fluid (ECF) concentrations of ganciclovir with plasma and CSF concentrations in a porcine model, using microdialysis during a 24 h period. Six Danish landrace pigs (female, age 4 months, 31-37 kg) received two weight-adjusted intravenous doses of ganciclovir. Unbound ganciclovir concentrations were determined by microdialysis over 24 h in five compartments: CSF (lateral ventricle, cisterna magna, and lumbar) and brain ECF (cortical and subcortical). Data were compared with paired plasma samples. Ganciclovir concentrations >IC
50 for CMV (1.6 µg/mL) were achieved in all compartments. Concentrations >IC
90 for CMV (8.3 µg/mL) were only achieved in plasma and the lumbar CSF compartment. The concentration time curves indicated higher lumbar and cisternal CSF concentrations than ECF concentrations. The ECF compartments achieved greater maximum concentration (C
max), area under the concentration time curve (AUC), and time >IC
50 after the second dose, and an accumulation ratio (R
ac) >1. The greater C
max, AUC, time >IC
50, and R
ac >1 in the ECF compartments with repeated dosages suggest that therapeutic concentrations may be achieved during long-term treatment. A higher loading dose might be warranted to improve early viral inhibition.
KW - Animals
KW - Antiviral Agents/pharmacokinetics
KW - Brain/metabolism
KW - Central Nervous System/metabolism
KW - Cytomegalovirus/drug effects
KW - Female
KW - Ganciclovir/pharmacokinetics
KW - Microdialysis
KW - Swine
KW - animal models
KW - antiviral agents
KW - CNS
KW - ganciclovir
KW - antiviral pharmacology
KW - microdialysis
KW - pharmacokinetics
UR - http://www.scopus.com/inward/record.url?scp=105004773513&partnerID=8YFLogxK
U2 - 10.1128/aac.01815-24
DO - 10.1128/aac.01815-24
M3 - Journal article
C2 - 40116478
SN - 0066-4804
VL - 69
JO - Antimicrobial Agents and Chemotherapy
JF - Antimicrobial Agents and Chemotherapy
IS - 5
M1 - e0181524
ER -