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1.
Figure 3

Figure 3. From: Absence or pharmacological blocking of placental P-glycoprotein profoundly increases fetal drug exposure.

Ratio of paclitaxel fetal concentration to maternal plasma concentration. Heterozygous mice were mated, and paclitaxel (10 mg/kg) was administered intravenously to pregnant dams at gestation day 15. At 1 hour after dosing, dams were euthanized, and fetuses from 4 litters were collected. Maternal plasma and fetal drug content and genotypes were determined as described in Methods. Open bars indicate wild-type values, hatched bars heterozygous values, and black bars Mdr1a–/–/1b–/– values. Values are expressed as mean paclitaxel concentration in fetal tissues (ng/g) normalized to maternal plasma paclitaxel concentration (ng/mL). Twelve to 14 fetuses of each genotype were analyzed. The average maternal plasma concentration was 1949 ± 219 ng/mL. Error bars indicate SD. AP < 0.0001 vs. wild-type fetuses in pairwise comparison.

Johan W. Smit, et al. J Clin Invest. 1999 Nov 15;104(10):1441-1447.
2.
Figure 1

Figure 1. From: Absence or pharmacological blocking of placental P-glycoprotein profoundly increases fetal drug exposure.

Ratio of [3H]digoxin fetal concentration to maternal plasma concentration. Heterozygous mice were mated, and [3H]digoxin (0.05 mg/kg) was administered intravenously to pregnant dams at gestation day 15. At 4 hours or 24 hours after dosing, dams were euthanized, and fetuses from 3 litters were collected. Maternal plasma and fetal drug content and genotypes were determined as described in Methods. Open bars indicate wild-type values, hatched bars heterozygous values, and black bars Mdr1a–/–/1b–/– values. Values are expressed as mean [3H]digoxin concentration in fetal tissues (ng/g) normalized to maternal plasma [3H]digoxin concentration (ng/mL). Six to 16 fetuses of each genotype were analyzed. Average maternal plasma concentrations were 19.2 ± 1.6 ng/mL and 1.1 ± 0.15 ng/mL at 4 and 24 hours after digoxin administration, respectively. Error bars indicate SD. AP < 0.0001, BP < 0.005, vs. wild-type fetuses in pairwise comparison.

Johan W. Smit, et al. J Clin Invest. 1999 Nov 15;104(10):1441-1447.
3.
Figure 2

Figure 2. From: Absence or pharmacological blocking of placental P-glycoprotein profoundly increases fetal drug exposure.

Ratio of [14C]saquinavir fetal concentration to maternal plasma concentration. Heterozygous mice were mated, and [14C]saquinavir (1 mg/kg) was administered intravenously to pregnant dams at gestation day 15. At 5 or15 minutes after dosing, dams were euthanized, and fetuses from 4 litters were collected. Maternal plasma and fetal drug content and genotypes were determined as described in Methods. Open bars indicate wild-type values, hatched bars heterozygous values, and black bars Mdr1a–/–/1b–/– values. Values are expressed as mean [14C]saquinavir concentration in fetal tissues normalized to maternal plasma [14C]saquinavir concentration. Four to 27 fetuses of each genotype were analyzed. Average maternal plasma concentration was 429 ± 32 ng/mL and 145.9 ± 16 ng/mL at 5 minutes and 15 minutes after [14C]saquinavir administration, respectively. All animals had also received oral administration of vehicle 2 hours before intravenous drug administration for proper comparison to PSC833-treated mice (see experiment described in Table ). Error bars indicate SD. AP < 0.005 vs. wild-type fetuses in pairwise comparison.

Johan W. Smit, et al. J Clin Invest. 1999 Nov 15;104(10):1441-1447.

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