PLoS ONE · 2019 · 19 citations · 24 references
MedicinePharmacokineticsPharmacologyBioavailabilityDrug DeliveryMaternal-fetal MedicineAntiretroviral TherapyHuman Immunodeficiency Virus PharmacotherapyMaternal-fetal PhysiologyPlacental BiologyPlacental PhysiologyPregnancy PharmacologyMaternal-fetal Concentration RatiosMaternal-fetal Drug TransferMaternal-fetal TransferPlacental Drug DispositionPlacental Drug TransportPlacental PharmacokineticsTransplacental ExposureTransplacental Transfer
OBJECTIVE: To determine the transplacental pharmacokinetics of the HIV integrase inhibitor dolutegravir. STUDY DESIGN: Maternal-to-fetal transfer across the term human placenta was investigated with the ex-vivo dually perfused cotyledon model, in 5 closed-circuit, recirculating experiments. Dolutegravir was added to a maternal perfusate containing antipyrine, a marker to validate the cotyledon's viability, and 2 g/liter of human albumin. RESULTS: After 3h of recirculating perfusion, the mean (± SD) DTG concentrations in the maternal and in the fetal compartments were respectively 2450 ± 286 ng/mL and 715 ± 369 ng/mL, with a fetal-to-maternal ratio of 34% ± 18% and a clearance index (in comparison with antipyrine transfer) of 79% ± 23%. The mean cotyledon accumulation index was 153% ± 25%. CONCLUSION: Fetal transplacental exposure to dolutegravir was considerable as well as accumulation in placental tissue. Whether this may lead to risks for the exposed fetus requires more investigation.
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Rebecca Zash, Denise L. Jacobson, Modiegi Diseko et al. · The Lancet Global Health · 2018 · 151 citations · Full text