Liposome-encapsulated hemoglobin (hemoglobin-vesicle) is not transferred from mother to fetus at the late stage of pregnancy in the rat model
2012
Kaga, Maiko | Li, Heng | Ohta, Hidenobu | Taguchi, Kazuaki | Ogaki, Shigeru | Izumi, Hitomi | Inagaki, Masumi | Tsuchiya, Shigeru | Okamura, Kunihiro | Otagiri, Masaki | Sakai, Hiromi | Yaegashi, Nobuo
AIMS: Liposome-encapsulated hemoglobin (hemoglobin vesicles: HbV; diameter 250nm) is reconstructed from human hemoglobin and developed as an artificial oxygen carrier for use as a transfusion alternative. Previous studies using rodent models closely investigated the safety of daily repeated infusions (DRI) of HbV and reported that the reticuloendothelial system was physiologically capable of degrading HbV to maintain plasma clinical chemistry within normal ranges. The present study examined the effect of DRI of HbV on the pregnant rat mother and fetal development, focusing on placental transfer of HbV in pregnancy. MAIN METHODS: Pregnant rats intravenously received HbV bolus injections at 2ml/kg/day for the last 7 consecutive days till term. The cumulative infusion volume (14ml/kg) was equal to 25% of the whole blood volume (56ml/kg). KEY FINDINGS: Maternal DRI of HbV had no obvious side effects on the pregnant mother or on fetal development. Maternal vital signs, plasma clinical chemistry, and blood gas parameters were overall normal after DRI of HbV. In addition, maternal/fetal transfer of HbV was limited to the placenta and HbV did not reach the fetus. Histopathological examination with human hemoglobin antibody detected HbV accumulation in the maternal spleen, liver, kidney, and placenta, but not in the fetuses. These results were also confirmed by a pharmacokinetic study using ¹²⁵I-labeled HbV. SIGNIFICANCE: This safety study of HbV use in the pregnant mother and fetus will contribute to a possible application of HbV as a potential treatment for fetal hypoxia by supplying oxygen through the placenta.
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