Carbamazepine and Its Metabolites in Human Perfused Placenta and in Maternal and Cord Blood
Autor: | T. Partanen, Riitta Herva, P. Arvela, P. Pienimäki, Kirsi Vähäkangas, Olavi Pelkonen, A.‐L. Hartikainen |
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Rok vydání: | 1995 |
Předmět: |
medicine.medical_specialty
Placental cotyledon Chromatography Gas Placenta High-performance liquid chromatography Mass Spectrometry Pregnancy Internal medicine medicine Humans Maternal-Fetal Exchange Chromatography High Pressure Liquid business.industry Biological Transport Metabolism Carbamazepine Fetal Blood Blood Fetal circulation medicine.anatomical_structure Endocrinology Neurology Cord blood Anesthesia Female Neurology (clinical) business Perfusion Antipyrine medicine.drug |
Zdroj: | Epilepsia. 36:241-248 |
ISSN: | 1528-1167 0013-9580 |
DOI: | 10.1111/j.1528-1157.1995.tb00991.x |
Popis: | Summary: Placental transfer and metabolism of carbamazepine (CBZ) was studied in a dual recirculating placental cotyledon perfusion system and was also evaluated in 16 pairs of maternal venous and cord blood samples. Among the parameters studied as possible indicators of a successful perfusion, volume changes in perfusate divided the perfusions into two groups, whereas no significant differences between perfusions were noted in blood gas analysis or in antipyrine transfer. CBZ added into the maternal circulation crosses the placenta in the beginning quicker than antipyrine which is in agreement with the different lipid solubilities of these compounds. Because the transfer rates of antipyrine and CBZ were about the same, the mechanism of transfer of CBZ is probably similar to that of antipyrine (passive diffusion). No metabolites of CBZ could be detected in the perfusate by high-performance liquid chromatography (HPLC) or gas chromatographyhass spectrometry. With the improved HPLC methodology for CBZ metabolites, six metabolites were detected in clinical samples, including 10-hydroxy-10, 11-dihydro-CBZ (10-OH-CBZ), which has been described earlier in only 1 uremic patient. Relative levels of metabolites showed significant individual differences. CBZ crosses perfused placenta rapidly, but this does not contribute to CBZ metabolites detected in maternal and fetal circulation. |
Databáze: | OpenAIRE |
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