Sebastian J. Padayatty, MRCP, PhD; He Sun, PhD, CBS; Yaohui Wang, MD; Hugh D. Riordan, MD; Stephen M. Hewitt, MD, PhD; Arie Katz, MD; Robert A. Wesley, PhD; Mark Levine, MD
Grant Support: By a grant from the National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health (Z01 DK 54506). Dr. Katz received partial support from the Office of Dietary Supplements, Office of the Director, National Institutes of Health.
Potential Financial Conflicts of Interest: None disclosed.
Requests for Single Reprints: Mark Levine, MD, Molecular and Clinical Nutrition Section, Building 10, Room 4D52-MSC 1372, National Institutes of Health, Bethesda, MD 20892-1372.
Current Author Addresses: Dr. Padayatty, Wang, and Levine: Molecular and Clinical Nutrition Section, Building 10, Room 4D52-MSC 1372, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD 20892-1372.
Dr. Sun: Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857.
Dr. Riordan: Bio-Communications Institute, 3100 North Hillside Avenue, Wichita, KS 67219.
Dr. Hewitt: National Cancer Institute, ATC 225D, MSC 4605, National Institutes of Health, Bethesda, MD 20802-4605.
Dr. Katz: Molecular and Clinical Nutrition Section, Building 10, Room 6C432B, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD 20892.
Dr. Wesley: Clinical Center, Building 10, Room 10S246-MSC 1871, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD 10892.
Author Contributions: Conception and design: S.J. Padayatty, H. Sun, Y. Wang, H.D. Riordan, S.M. Hewitt, M. Levine.
Analysis and interpretation of the data: S.J. Padayatty, H. Sun, Y. Wang, A. Katz, R.A. Wesley, M. Levine.
Drafting of the article: S.J. Padayatty, A. Katz, M. Levine.
Critical revision of the article for important intellectual content: S.J. Padayatty, H. Sun, Y. Wang, H.D. Riordan, S.M. Hewitt, A. Katz, M. Levine.
Final approval of the article: S.J. Padayatty, H. Sun, Y. Wang, H.D. Riordan, S.M. Hewitt, A. Katz, M. Levine.
Provision of study materials or patients: H.D. Riordan, M. Levine.
Statistical expertise: R.A. Wesley.
Obtaining of funding: M. Levine.
Administrative, technical, or logistic support: Y. Wang, M. Levine.
Collection and assembly of data: S.J. Padayatty, H. Sun, Y. Wang, H.D. Riordan, A. Katz, M. Levine.
Vitamin C at high concentrations is toxic to cancer cells in vitro. Early clinical studies of vitamin C in patients with terminal cancer suggested clinical benefit, but 2 double-blind, placebo-controlled trials showed none. However, these studies used different routes of administration.
To determine whether plasma vitamin C concentrations vary substantially with the route of administration.
Dose concentration studies and pharmacokinetic modeling.
Academic medical center.
17 healthy hospitalized volunteers.
Vitamin C plasma and urine concentrations were measured after administration of oral and intravenous doses at a dose range of 0.015 to 1.25 g, and plasma concentrations were calculated for a dose range of 1 to 100 g.
Peak plasma vitamin C concentrations were higher after administration of intravenous doses than after administration of oral doses (P < 0.001), and the difference increased according to dose. Vitamin C at a dose of 1.25 g administered orally produced mean (±sd) peak plasma concentrations of 134.8 ± 20.6 µmol/L compared with 885 ± 201.2 µmol/L for intravenous administration. For the maximum tolerated oral dose of 3 g every 4 hours, pharmacokinetic modeling predicted peak plasma vitamin C concentrations of 220 µmol/L and 13 400 µmol/L for a 50-g intravenous dose. Peak predicted urine concentrations of vitamin C from intravenous administration were 140-fold higher than those from maximum oral doses.
Patient data are not available to confirm pharmacokinetic modeling at high doses and in patients with cancer.
Oral vitamin C produces plasma concentrations that are tightly controlled. Only intravenous administration of vitamin C produces high plasma and urine concentrations that might have antitumor activity. Because efficacy of vitamin C treatment cannot be judged from clinical trials that use only oral dosing, the role of vitamin C in cancer treatment should be reevaluated.
Clinical studies of vitamin C as a potential anticancer agent have produced inconsistent results despite in vitro evidence that high concentrations kill cancer cells.
Pharmacokinetic studies in healthy persons, using a depletion-repletion design, show that intravenous administration can achieve 70-fold higher blood levels of vitamin C than the highest tolerated oral dose.
Although this study provides better understanding of the pharmacokinetic issues involved in research on vitamin C, it provides no evidence that vitamin C has any effect on cancer cells and cannot be used to support its clinical use for therapeutic purposes.
Plasma vitamin C concentrations in healthy volunteers after intravenous or oral administration of vitamin C.Inset:
Predicted plasma vitamin C concentrations in healthy persons after oral (top) or intravenous (IV) (bottom) administration of vitamin C.
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Padayatty SJ, Sun H, Wang Y, et al. Vitamin C Pharmacokinetics: Implications for Oral and Intravenous Use. Ann Intern Med. 2004;140:533–537. doi: 10.7326/0003-4819-140-7-200404060-00010
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Published: Ann Intern Med. 2004;140(7):533-537.
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