Search Results - "Yu, Dale K."

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  1. 1

    The Contribution of P-glycoprotein to Pharmacokinetic Drug-Drug Interactions by Yu, Dale K.

    Published in Journal of clinical pharmacology (01-12-1999)
    “…P‐glycoprotein (PGP) is well known because of its contribution to multiple‐drug resistance during anticancer treatment. More recent work indicates that PGP…”
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    Journal Article
  2. 2

    Effect of food coadministration on 5-aminosalicylic acid oral suspension bioavailability by Yu, D K, Elvin, A T, Morrill, B, Eichmeier, L S, Lanman, R C, Lanman, M B, Giesing, D H

    Published in Clinical pharmacology and therapeutics (01-07-1990)
    “…Single doses of 1 gm 5-aminosalicylic acid (5-ASA) suspension was administered to 24 healthy volunteers during both fasting and fed conditions. For subjects in…”
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    Journal Article
  3. 3

    Pharmacokinetics of dothiepin in humans: a single dose dose-proportionality study by Yu, D K, Dimmitt, D C, Lanman, R C, Giesing, D H

    Published in Journal of pharmaceutical sciences (01-06-1986)
    “…Dothiepin hydrochloride (N,N-dimethyldibenzo[b,e]thiepin-delta 11(6 H), gamma-propylamine hydrochloride) is a tricyclic antidepressant which is structurally…”
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  4. 4

    A limited sampling method for the estimation of vigabatrin maximum plasma concentration and area under the curve by TAMMARA, V, MAHMOOD, I, YU, D. K, HILEMAN, G. A

    Published in Therapeutic drug monitoring (01-02-1997)
    “…A limited sampling model (LSM) was developed to estimate the area under the curve (AUC) and maximum plasma concentration (Cmax) for a 1-g oral dose of…”
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  5. 5

    Selection of Doses for Phase II Clinical Trials Based on Pharmacokinetic Variability Consideration by Yu, Dale K., Bhargava, Vijay O., Weir, Scott J.

    Published in Journal of clinical pharmacology (01-08-1997)
    “…Pharmacokinetic variability is an important component of the total variability in drug response, but Phase II dose‐response trials frequently are designed…”
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  6. 6

    Pharmacokinetics of propylene glycol in humans during multiple dosing regimens by Yu, D K, Elmquist, W F, Sawchuk, R J

    Published in Journal of pharmaceutical sciences (01-08-1985)
    “…The pharmacokinetics of propylene glycol has been examined during multiple oral-dosing regimens. The glycol is rapidly absorbed, with Cpmax observed within 1 h…”
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  7. 7

    A comparison of population and standard two-stage pharmacokinetic analyses of vigabatrin data by Yu, D K, Hutcheson, S J, Wei, G, Bhargava, V O, Weir, S J

    Published in Biopharmaceutics & drug disposition (01-08-1994)
    “…Vigabatrin (VGB), an irreversible inhibitor of GABA, is being developed as an add-on therapy for uncontrolled complex partial seizure. A single-dose study was…”
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  8. 8

    Population pharmacokinetics of teicoplanin in patients with endocarditis by Yu, D K, Nordbrock, E, Hutcheson, S J, Lewis, E W, Sullivan, W, Bhargava, V O, Weir, S J

    “…Teicoplanin is a new glycopeptide antibiotic, active against aerobic and anaerobic gram-positive bacteria. The drug is intended for the treatment of systemic…”
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  9. 9

    Pharmacokinetics of nitroglycerin and metabolites in humans following oral dosing by Yu, D K, Williams, R L, Benet, L Z, Lin, E T, Giesing, D H

    Published in Biopharmaceutics & drug disposition (01-11-1988)
    “…Single dose oral nitroglycerin (GTN) was administered to six healthy subjects as 6.5, 9.0, and 13.0 mg aqueous solutions in sequential study phases to…”
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  10. 10

    Pharmacokinetics of diltiazem and propranolol when administered alone and in combination by Dimmitt, D C, Yu, D K, Elvin, A T, Giesing, D H, Lanman, R C

    Published in Biopharmaceutics & drug disposition (01-10-1991)
    “…Multiple oral doses of diltiazem (DTZ) and propranolol (PPL, 60 mg every 8 h daily for 13 doses) were administered to 14 healthy volunteers alone and in…”
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  11. 11

    Pharmacokinetics of propylene glycol in the rabbit by Yu, D K, Sawchuk, R J

    “…Propylene glycol (PG) is widely used as a drug solvent in the pharmaceutical industry. However, it has produced central nervous system toxicity during chronic…”
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