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Image Search Results
Journal: The Journal of Pharmacology and Experimental Therapeutics
Article Title: Pharmacokinetic Assessment of Cooperative Efflux of the Multitargeted Kinase Inhibitor Ponatinib Across the Blood-Brain Barrier
doi: 10.1124/jpet.117.246116
Figure Lengend Snippet: Total plasma (solid line with square) concentration and brain (dashed line with circle) concentration in wild-type mice (A) and Mdr1a/b(−/−)Bcrp1(−/−) mice (B), and brain-to-plasma ratio time course of ponatinib after administration of a single intravenous bolus (3 mg/kg) in FVB wild-type and Mdr1a/b(−/−)Bcrp1(−/−) mice (N = 3 to 4 at each time point) (C). Data are presented as the mean ± S.D.
Article Snippet: Animals Pharmacokinetic studies were conducted using
Techniques: Concentration Assay
Journal: The Journal of Pharmacology and Experimental Therapeutics
Article Title: Pharmacokinetic Assessment of Cooperative Efflux of the Multitargeted Kinase Inhibitor Ponatinib Across the Blood-Brain Barrier
doi: 10.1124/jpet.117.246116
Figure Lengend Snippet: Pharmacokinetic/metric parameters estimated from NCA of total brain and plasma concentration-time profiles after administration of a single intravenous bolus of ponatinib (3 mg/kg) in FVB wild-type and Mdr1a/b(−/−)Bcrp1(−/−) mice ( N = 3 to 4 at each time point) Data are presented as mean or mean ± S.E.M, unless otherwise indicated.
Article Snippet: Animals Pharmacokinetic studies were conducted using
Techniques: Concentration Assay, Mouse Assay
Journal: The Journal of Pharmacology and Experimental Therapeutics
Article Title: Pharmacokinetic Assessment of Cooperative Efflux of the Multitargeted Kinase Inhibitor Ponatinib Across the Blood-Brain Barrier
doi: 10.1124/jpet.117.246116
Figure Lengend Snippet: Total plasma (solid line with square) and brain (dashed line with circle) concentration-time profiles after administration of a single oral dose (30 mg/kg) of ponatinib in FVB wild-type (A), Bcrp1(−/−) (B), Mdr1a/b(−/−) (C), and Mdr1a/b(−/−)Bcrp1(−/) (D) mice (N = 4 at each time point). Data are presented as mean ± S.D. Data for the wild-type mice were previously reported (Laramy et al., 2017) and included in this present study to compare the wild-type genotype with the three other genotypes that lack efflux transporters.
Article Snippet: Animals Pharmacokinetic studies were conducted using
Techniques: Concentration Assay
Journal: The Journal of Pharmacology and Experimental Therapeutics
Article Title: Pharmacokinetic Assessment of Cooperative Efflux of the Multitargeted Kinase Inhibitor Ponatinib Across the Blood-Brain Barrier
doi: 10.1124/jpet.117.246116
Figure Lengend Snippet: Total brain-to-plasma ratio profiles after administration of a single oral dose (30 mg/kg) in FVB wild-type, Bcrp1(−/−), Mdr1a/b(−/−), and Mdr1a/b(−/−)Bcrp1(−/−) mice (N = 4 at each time point). Data are presented as the mean ± S.D. Data for the wild-type were previously reported (Laramy et al., 2017) and were included in this present study to compare the wild-type genotype with the three other genotypes that lack efflux transporters.
Article Snippet: Animals Pharmacokinetic studies were conducted using
Techniques:
Journal: The Journal of Pharmacology and Experimental Therapeutics
Article Title: Pharmacokinetic Assessment of Cooperative Efflux of the Multitargeted Kinase Inhibitor Ponatinib Across the Blood-Brain Barrier
doi: 10.1124/jpet.117.246116
Figure Lengend Snippet: Pharmacokinetic/metric parameters determined by NCA of total brain and plasma concentration-time profiles after a single oral dose (30 mg/kg) of ponatinib in FVB wild-type, Bcrp1(−/−) , Mdr1a/b(−/−) , and Mdr1a/b(−/−)Bcrp1(−/−) mice ( N = 4 at each time point) Data are presented as the mean or mean ± S.E.M, unless otherwise indicated. Data for the wild-type mice were previously reported ( Laramy et al., 2017 ) and are included in this present study to compare with the three other genotypes that lack efflux transporters.
Article Snippet: Animals Pharmacokinetic studies were conducted using
Techniques: Concentration Assay, Mouse Assay
Journal: The Journal of Pharmacology and Experimental Therapeutics
Article Title: Pharmacokinetic Assessment of Cooperative Efflux of the Multitargeted Kinase Inhibitor Ponatinib Across the Blood-Brain Barrier
doi: 10.1124/jpet.117.246116
Figure Lengend Snippet: Total steady-state plasma and brain concentrations (A) and corresponding total steady-state brain-to-plasma ratios (B) of ponatinib after continuous intraperitoneal infusion (40 µg/h) for 48 hours in FVB wild-type, Bcrp1(−/−), Mdr1a/b(−/−), and Mdr1a/b(−/−)Bcrp1(−/−) mice (N = 4 in each genotype) (*P < 0.05; *statistical significance). Data are presented as the mean ± S.D.
Article Snippet: Animals Pharmacokinetic studies were conducted using
Techniques:
Journal: The Journal of Pharmacology and Experimental Therapeutics
Article Title: Pharmacokinetic Assessment of Cooperative Efflux of the Multitargeted Kinase Inhibitor Ponatinib Across the Blood-Brain Barrier
doi: 10.1124/jpet.117.246116
Figure Lengend Snippet: Observed (red square) and model-predicted (red solid line) total plasma concentration-time profiles, and observed (black circle) and model-predicted (black dashed line) total brain concentration-time profiles in FVB wild-type (A) and Mdr1a/b(−/−)Bcrp1(−/−) (B) mice (N = 3 to 4 at each time point) after a single intravenous bolus (3 mg/kg). The observed data are presented as the mean ± S.D.
Article Snippet: Animals Pharmacokinetic studies were conducted using
Techniques: Concentration Assay
Journal: The Journal of Pharmacology and Experimental Therapeutics
Article Title: Pharmacokinetic Assessment of Cooperative Efflux of the Multitargeted Kinase Inhibitor Ponatinib Across the Blood-Brain Barrier
doi: 10.1124/jpet.117.246116
Figure Lengend Snippet: Observed (red square) and model-predicted (red solid line) total plasma concentration-time profiles, and observed (black circle) and model-predicted (black dashed line) total brain concentration-time profiles in FVB wild-type (A), Bcrp1(−/−) (B), Mdr1a/b(−/−) (C), and Mdr1a/b(−/−)Bcrp1(−/−) (D) mice (N = 4 at each time point) after a single oral dose (30 mg/kg). The observed data are presented as the mean ± S.D. The observed data for the wild-type were previously reported (Laramy et al., 2017) and were included in this present study to compare with the three other genotypes that lack efflux transporters.
Article Snippet: Animals Pharmacokinetic studies were conducted using
Techniques: Concentration Assay
Journal: PLoS ONE
Article Title: Reduced Androgen Receptor Expression Accelerates the Onset of ERBB2 Induced Breast Tumors in Female Mice
doi: 10.1371/journal.pone.0060455
Figure Lengend Snippet: A. Breeding strategy used to create experimental cohorts. Two generation breeding was used to produce tumor-prone MMTV-NeuNT (activated rat ERBB2) transgenic MARKO (male and females underlined on the left side) and Control (underlined on the right) mice. MARKO mice are positive for MMTV-cre transgene, specifically expressed in mammary glands. B. Recombination events in the genomic DNA from mammary ductal tissue dissociated from fat cells. Top band (952 bp) is derived from the non-recombined floxed Ar fl allele, middle band (855 bp) is from the wild-type Ar + allele, and the lower band (404 bp) is an amplicon derived from the Ar Δ allele, resulting from Cre/LoxP induced deletion of exon 2. Ar fl /+ is a positive control for the floxed allele and WT is wild-type ( Ar + /Ar + ). Left panel is recombination in male mice and the right panel is recombination in female mice. No recombination is observed in mice lacking MMTV-cre (lanes 1 and 4), the deleted allele is present in mice with MMTV-cre (lanes 2 and 3) C. Reduced number of AR positive luminal epithelial cells in MARKO mammary glands. AR positive luminal epithelial cells in the mammary glands of Control (n = 5) and MARKO (n = 5) mice were counted and determined as a percentage of the total number of cells per gland (p = 0.0019). An average of 260 cells were counted per individual mouse. Immunohistochemical staining for AR expression in Control (D) and MARKO (E and F) mammary glands. Scale bar = 20 µm.
Article Snippet:
Techniques: Transgenic Assay, Control, Derivative Assay, Amplification, Positive Control, Immunohistochemical staining, Staining, Expressing