Co-Directors:
Mitch A. Phelps, PhD
Steven K. Clinton, MD, PhD
For orders or inquiries, please email phasr@osumc.edu
Expertise among the PhASR personnel includes quantitative pharmacology; bioanalytical methodology, design of pharmacokinetic/pharmacodynamic studies in animal disease models and in humans enrolled in clinical trials; data analysis and modeling of PK/PD data to inform drug development decisions. The PhASR personnel are available for consultation on clinical or pre-clinical PK/PD experimental design and analysis.
Key program objectives
PhASR’s Specific Aims are to:
- Aim 1: Develop and update and validate new assays to quantify drugs, metabolites, endogenous biomolecules/biomarkers, environmental carcinogens, nutrients and bioactive phytochemicals in biospecimens, as well as environmental and food sources.
- Aim 2: Apply validated assays to quantify drug and metabolite concentrations in biological matrices and conduct PK/PD studies for incorporation into preclinical and clinical studies to support evidence-based decision-making.
- Aim 3: Provide expertise in targeted nutritional lipidomics to support studies of foods and dietary patterns in preclinical, clinical and epidemiologic studies.
- Aim 4: Provide expertise in study design, biosample procurement and processing, and data analysis and interpretation to support submission of clinical trial protocols, grant applications and publications.
Contact PhASR
Pharmacoanalytical Shared Resource
College of Pharmacy, Division of Pharmaceutics
241 Parks Hall
500 W. 12th Ave.
Columbus, OH 43210
441 Biomedical Research Tower
460 W. 12th Ave.
Columbus, OH 43210
Availability: Monday-Friday, 8 a.m.-5 p.m.
This Shared Resource is supported by the Cancer Center Support Grant (P30CA016058).