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Elimination of 11-nor-delta-9-tetrahydrocannabinol-9-carboxylic acid when normalized to urinary creatinine

Creator:: Beardsley, Grant D.
Resource Type:: Masters Thesis
Full Text:: approved: Redacted for Privacy fJohn Mark Chiistensen Gas chromatography mass/spectrometry quantitative

Analysis of nonlinear pharmacokinetic systems and the nonlinear disposition of phenylbutazone in equine (horses)

Creator:: Ma, Lian
Abstract:: The first part of the dissertation is to evaluate the use of proposed and established equations for area under the plasma concentration versus time (AUC) for molecules undergoing nonlinear Michaelis–Menten pharmacokinetic elimination. The effects of varying Michaelis-Menten parameters, rate of drug absorption, or bioavailability on the predictability of drug exposure...
Resource Type:: Dissertation
Full Text:: : John Mark Christensen The first part of the dissertation is to evaluate the use of proposed and

Vehicle and enhancer effects on penetration of acyclovir through chicken and cockatiel skin in vitro

Creator:: Ruan, Xiumei
Resource Type:: Masters Thesis
Full Text:: . I would also like to express my sincere appreciation to my adviser, Dr. J.M. Christensen for his

Disposition of C H N O S in rats and three antiulcer agents in llamas

Creator:: Limsakun, Tharin
Resource Type:: Dissertation
Full Text:: Llamas Abstract approved: John Mark Christensen, Ph.D. The solubility and disposition of a new

Fish oral antigen delivery system development and optimization

Creator:: Zhang, Jia Ai (Allen)
Abstract:: Oral administration is the most practical way of vaccination of fish. It has advantages over intraperitoneal injection and immersion methods that include no stressful handling, no interference with routine fish husbandry and antigens can be delivered to the fish in their feed. An oral antigen delivery system was developed for...
Resource Type:: Dissertation
Full Text:: Optimization Abstract Approved: John Mark Christensen, Ph.D. Oral administration is the most practical

Pharmacokinetics of ampicillin, gentamicin, amikacin, and omeprazole in llamas

Creator:: Kasiwong, Srirat
Resource Type:: Dissertation
Full Text:: , Amikacin and Omeprazole in Llamas. Abstract approved: John Mark Christensen Ampicillin sodium and

1) Preparation of Acetaminophen Capsules Containing Beads Prepared by Hot-melt Direct Blend Coating Method 2) Pharmacokinetic Modeling and Monte Carlo Simulations in The Context of Additional Criteria for Bioequivalence Assessments 3) Pharmacokinetic Prediction of Levofloxacin Accumulation in Tissue and its Association to Tendinopathy

Creator:: Pham, Loan
Abstract:: The thrust of this thesis is to study oral solid dosage formulation using hot melt coating method and to use pharmacokinetic modeling and simulation (PK M&S) as a tool that can help to predict pharmacokinetics of a drug in human and the probability of passing various bioequivalence criteria of the...
Resource Type:: Dissertation
Full Text:: would like to thank my advisor, Dr. John Mark Christensen, who from the initial research stage was

Stability of oral liquid cimetidine HCl and furosemide repackaged in unit dose containers at various temperatures

Creator:: Lee, Rai-yun
Resource Type:: Masters Thesis
Full Text:: approved:Redacted for Privacy Dr. J. Mark Christensen Oral liquid cimetidine HC1 or furosemide were repackaged

Comparison of pharmacokinetic data analysis with two competing pharmacokinetic software program

Creator:: Karnpracha, Chanida
Abstract:: Pharmacokinetics (PK) is the study of the transit of drug into, within and removal from the body to reveal how the body acts on a drug when it is taken. There are four major areas in PK: absorption, distribution, metabolism and elimination. Pharmacokinetics research can be separated into two areas:...
Resource Type:: Masters Thesis
Full Text:: : J. Mark Christensen Pharmacokinetics (PK) is the study of the transit of drug into, within and

Formulation of an oral acetylsalicylic acid suspension and pharmacokinetics of parenteral thrombomodulin analogues

Creator:: Piepmeier, Edward H.
Abstract:: Sustained concentrations of active compound were maintained in vitro and in vivo for an oral and a parenteral dosage form respectively. The vehicle of a oral dosage form was modified and the molecular structure of a parenteral dosage form was modified. An oral dosage form was tested in vitro using...
Resource Type:: Dissertation
Full Text:: Analogues. 1"? Abstract approved: Redacted for Privacy Mark Christensen, rn. v. Sustained c

ScholarsArchive@OSU

Elimination of 11-nor-delta-9-tetrahydrocannabinol-9-carboxylic acid when normalized to urinary creatinine

Analysis of nonlinear pharmacokinetic systems and the nonlinear disposition of phenylbutazone in equine (horses)

Vehicle and enhancer effects on penetration of acyclovir through chicken and cockatiel skin in vitro

Disposition of C H N O S in rats and three antiulcer agents in llamas

Fish oral antigen delivery system development and optimization

Pharmacokinetics of ampicillin, gentamicin, amikacin, and omeprazole in llamas

Stability of oral liquid cimetidine HCl and furosemide repackaged in unit dose containers at various temperatures

Comparison of pharmacokinetic data analysis with two competing pharmacokinetic software program

Formulation of an oral acetylsalicylic acid suspension and pharmacokinetics of parenteral thrombomodulin analogues

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