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Walter Wolf

Researcher at University of Southern California

Publications -  93
Citations -  1947

Walter Wolf is an academic researcher from University of Southern California. The author has contributed to research in topics: Pharmacokinetics & Radical. The author has an hindex of 24, co-authored 93 publications receiving 1902 citations. Previous affiliations of Walter Wolf include United States Department of Veterans Affairs & National Autonomous University of Mexico.

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Tumor trapping of 5-fluorouracil: in vivo 19F NMR spectroscopic pharmacokinetics in tumor-bearing humans and rabbits

TL;DR: These studies document that NMR spectroscopy is clinically feasible in vivo, allows noninvasive pharmacokinetic analyses at a drug-target tissue in real time, and may produce therapeutically important information at the time of drug administration.
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Fluorine-19 NMR spectroscopic studies of the metabolism of 5-fluorouracil in the liver of patients undergoing chemotherapy

TL;DR: These observations represent the first noninvasive NMR study of drugs in human patients and show the feasibility of using in vivo F-19 NMR spectroscopy for human studies of fluorinated compounds.
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19F-MRS studies of fluorinated drugs in humans

TL;DR: The use of 19F-NMR as a noninvasive probe to measure directly the pharmacokinetics of drugs at their target (effector) site(s) is illustrated in this article by human studies with 5-fluorouracil and other fluoropyrimidines.
Journal Article

Radiogallium Localization in Tumors: Blood Binding and Transport and the Role of Transferrin

TL;DR: It is demonstrated that gallium at the tracer level in blood is exclusively bound to and transported by transferrin, and indicates that electrophoresis and dialysis of easily dissociable metal complexes are subject to significant artifacts.
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Human tumor fluorouracil trapping: clinical correlations of in vivo 19F nuclear magnetic resonance spectroscopy pharmacokinetics.

TL;DR: Evaluating the pharmacokinetics of 5FU in the tumors of 11 patients with carcinoma of the breast, colon, endometrium, cervix, and kidney using 19F-NMRS concludes that NMRS is clinically feasible, and enables investigators to study 5FU pharmacokinetic and metabolism in tumors in vivo.