Search Results - "Boulton, D. W."

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  1. 1

    Effects of rifampin and mefenamic acid on the pharmacokinetics and pharmacodynamics of dapagliflozin by Kasichayanula, S., Liu, X., Griffen, S. C., LaCreta, F. P., Boulton, D. W.

    Published in Diabetes, obesity & metabolism (01-03-2013)
    “…Aims Dapagliflozin is a selective sodium glucose cotransporter 2 (SGLT2) inhibitor that decreases serum glucose by reducing renal glucose reabsorption, thereby…”
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  2. 2

    Evaluation of 4β‐Hydroxycholesterol as a Clinical Biomarker of CYP3A4 Drug Interactions Using a Bayesian Mechanism–Based Pharmacometric Model by Leil, TA, Kasichayanula, S, Boulton, DW, LaCreta, F

    “…A Bayesian mechanism–based pharmacokinetic/pharmacodynamic model of cytochrome P450 3A4 (CYP3A4) activity was developed based on a clinical study of the…”
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  3. 3

    Lack of a pharmacokinetic drug-drug interaction between lithium and valproate when co-administered with aripiprazole by Boulton, D. W., Kollia, G. D., Mallikaarjun, S., Kornhauser, D. M.

    “…Summary What is known and Objective:  The antipsychotic, aripiprazole, plus lithium or valproate demonstrates rapid and significant improvement in manic…”
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  4. 4

    The pharmacokinetics of standard antidepressants with aripiprazole as adjunctive therapy: studies in healthy subjects and in patients with major depressive disorder by Boulton, DW, Balch, AH, Royzman, K., Patel, CG, Berman, RM, Mallikaarjun, S., Reeves, RA

    Published in Journal of psychopharmacology (Oxford) (01-04-2010)
    “…Possible effects of the atypical antipsychotic aripiprazole on the pharmacokinetics of standard antidepressant therapies (ADTs) were assessed in two…”
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  5. 5

    Fate of the Flavonoid Quercetin in Human Cell Lines: Chemical Instability and Metabolism by BOULTON, DAVID W., WALLE, U. KRISTINA, WALLE, THOMAS

    Published in Journal of pharmacy and pharmacology (01-03-1999)
    “…Although cell cultures are increasingly being used as models for studying the biological actions of flavonoids, no information on the fate, such as uptake and…”
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  6. 6

    A Nonlinear Mixed Effects Pharmacokinetic Model for Dapagliflozin and Dapagliflozin 3‐O‐glucuronide in Renal or Hepatic Impairment by Walt, J‐S, Hong, Y, Zhang, L, Pfister, M, Boulton, DW, Karlsson, MO

    “…Dapagliflozin is a sodium–glucose co‐transporter 2 inhibitor in development for the treatment of type 2 diabetes mellitus. A semi‐mechanistic population…”
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  7. 7

    Effect of St. John's wort ( Hypericum perforatum) on cytochrome P-450 2D6 and 3A4 activity in healthy volunteers by Markowitz, J.S., DeVane, C.L., Boulton, D.W., Carson, S.W., Nahas, Z., Risch, S.C.

    Published in Life sciences (1973) (21-01-2000)
    “…The effects of the herb St. John's wort ( Hypericum perforatum), a purported antidepressant, on the activity of cytochrome P-450 (CYP) 2D6 and 3 A4 was…”
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  8. 8

    Pharmacokinetics and pharmacodynamics of dapagliflozin, a novel selective inhibitor of sodium-glucose co-transporter type 2, in Japanese subjects without and with type 2 diabetes mellitus by Kasichayanula, S, Chang, M, Hasegawa, M, Liu, X, Yamahira, N, LaCreta, F.P, Imai, Y, Boulton, D.W

    Published in Diabetes, obesity & metabolism (01-04-2011)
    “…Aims: Dapagliflozin, a selective, orally active inhibitor of the renal sodium-glucose co-transporter type 2 (SGLT2) is in development for the treatment of type…”
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  9. 9

    Comparison of the pharmacokinetics and pharmacodynamics of dapagliflozin in patients with type 1 versus type 2 diabetes mellitus by Tang, W., Leil, T. A., Johnsson, E., Boulton, D. W., LaCreta, F.

    Published in Diabetes, obesity & metabolism (01-03-2016)
    “…Aims To compare the pharmacokinetics and pharmacodynamics of dapagliflozin in patients with type 1 diabetes mellitus (T1DM) versus type 2 diabetes mellitus…”
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  10. 10

    Enantioselective disposition of salbutamol in man following oral and intravenous administration by BOULTON, D. W., FAWCETT, J. P.

    Published in British journal of clinical pharmacology (01-01-1996)
    “…1 Salbutamol is a β2,‐adrenoceptor stimulant used clinically as a racemate where the activity resides predominantly in the (‐)R enantiomer with little or no…”
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  11. 11

    Pharmacokinetics and pharmacodynamics of dapagliflozin in children and adolescents with type 2 diabetes mellitus by Tirucherai, G. S., LaCreta, F., Ismat, F. A., Tang, W., Boulton, D. W.

    Published in Diabetes, obesity & metabolism (01-07-2016)
    “…Aims To evaluate the pharmacokinetic (PK)/pharmacodynamic (PD) and safety profile of dapagliflozin in paediatric patients aged 10–17 years with type 2 diabetes…”
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  12. 12

    Extensive Binding of the Bioflavonoid Quercetin to Human Plasma Proteins by BOULTON, DAVID W., WALLE, U. KRISTINA, WALLE, THOMAS

    Published in Journal of pharmacy and pharmacology (01-02-1998)
    “…Although the bioflavonoids, a large group of polyphenolic natural products, exert chemopreventive effects in cardiovascular disease and cancer, there is little…”
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  13. 13

    Comparison of the exposure-response relationship of dapagliflozin in adult and paediatric patients with type 2 diabetes mellitus by Parkinson, J., Tang, W., Johansson, C-C., Boulton, D. W., Hamrén, B.

    Published in Diabetes, obesity & metabolism (01-07-2016)
    “…Aims To quantitatively compare the exposure–response relationship of dapagliflozin in adult and paediatric patients with type 2 diabetes mellitus (T2DM) and to…”
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  14. 14

    Lack of pharmacokinetic interaction between dapagliflozin, a novel sodium-glucose transporter 2 inhibitor, and metformin, pioglitazone, glimepiride or sitagliptin in healthy subjects by Kasichayanula, S, Liu, X, Shyu, W.C, Zhang, W, Pfister, M, Griffen, S.C, Li, T, LaCreta, F.P, Boulton, D.W

    Published in Diabetes, obesity & metabolism (2011)
    “…Aims: Dapagliflozin increases urinary glucose excretion by selectively inhibiting renal sodium-glucose transporter 2, an insulin-independent mechanism of…”
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  15. 15

    The pharmacokinetics of levosalbutamol : What are the clinical implications? by BOULTON, David W, FAWCETT, J. Paul

    Published in Clinical pharmacokinetics (2001)
    “…Salbutamol (albuterol) is a beta2-adrenoceptor agonist used as a bronchodilator for the treatment of asthma and as a uterine relaxant for the suspension of…”
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  16. 16

    Effect of a high-fat meal on the pharmacokinetics of dapagliflozin, a selective SGLT2 inhibitor, in healthy subjects by Kasichayanula, S., Liu, X., Zhang, W., Pfister, M., Reele, S. B., Aubry, A.-F., LaCreta, F. P., Boulton, D. W.

    Published in Diabetes, obesity & metabolism (01-08-2011)
    “…Dapagliflozin is a potent and selective inhibitor of sodium–glucose co‐transporter type 2 that is being developed for the treatment of type 2 diabetes…”
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  17. 17

    Saxagliptin, a potent, selective inhibitor of DPP-4, does not alter the pharmacokinetics of three oral antidiabetic drugs (metformin, glyburide or pioglitazone) in healthy subjects by Patel, C. G., Kornhauser, D., Vachharajani, N., Komoroski, B., Brenner, E., Handschuh del Corral, M., Li, L., Boulton, D. W.

    Published in Diabetes, obesity & metabolism (01-07-2011)
    “…Aim: To evaluate the pharmacokinetic interactions of the potent, selective, dipeptidyl peptidase‐4 inhibitor, saxagliptin, in combination with metformin,…”
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  18. 18

    Effect of saxagliptin on the pharmacokinetics of the active components of Ortho-Cyclen®, a combined oral contraceptive containing ethinyl estradiol and norgestimate, in healthy women by Upreti, V. V., Hsiang, C. B., Li, L., Xu, X., LaCreta, F. P., Boulton, D. W.

    Published in Diabetes, obesity & metabolism (01-12-2012)
    “…Saxagliptin (Onglyza™) is a dipeptidyl peptidase‐4 (DPP4) inhibitor for treating type 2 diabetes mellitus. This open‐label, randomized, two‐way crossover study…”
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  19. 19

    Pharmacokinetics and pharmacodynamics of single oral doses of albuterol and its enantiomers in humans by BOULTON, D. W, FAWCETT, J. P

    Published in Clinical pharmacology and therapeutics (01-08-1997)
    “…Albuterol (INN, salbutamol) is a beta 2-adrenergic receptor agonist widely used in the treatment of asthma. It is administered clinically as a racemic mixture,…”
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  20. 20

    Disposition of Morphine in Tissues of the Pregnant Rat and Foetus Following Single and Continuous Intraperitoneal Administration to the Mother by DEVANE, C. L., SIMPKINS, J. W., BOULTON, D. W., LAIZURE, S. C., MILLER, R. L.

    Published in Journal of pharmacy and pharmacology (01-11-1999)
    “…Foetal exposure to maternally administered opiates such as morphine represent a serious human health problem but disposition studies in man are difficult to…”
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