Nielsen · Basic & clinical pharmacology & toxicology 2015 · prospective single-arm pharmacokinetic study · n=10

Elimination of ascorbic acid after high-dose infusion in prostate cancer patients: a pharmacokinetic evaluation.

Cited 73 times in the scientific literature.

Level 4 - case-series / case-control

Single-arm uncontrolled pharmacokinetic study

PubMed 25220574 · doi:10.1111/bcpt.12323 · record verified 2026-08-30

What was done

Ten patients with metastatic prostate cancer received fixed intravenous ascorbic acid infusions at doses of 5, 30, and 60 g over a 4-week period. Serial plasma ascorbic acid levels were measured consecutively to evaluate pharmacokinetic parameters across the dosing range.

What was found

Ascorbic acid displayed first-order elimination kinetics throughout the dosing range. A 60 g IV dose produced a peak plasma concentration of 20.3 mM. The mean elimination half-life was 1.87 ± 0.40 hr, volume of distribution was 0.19 ± 0.05 L/kg, and clearance was 6.02 L/hr (100 mL/min). No differences in pharmacokinetic parameters were observed between weeks or doses.

Why it matters

This study provides human pharmacokinetic benchmarks for high-dose intravenous ascorbic acid, demonstrating that its rapid clearance prevents post-infusion maintenance of potentially cytotoxic concentrations without continuous maintenance dosing.

Limits

The study is limited by a very small sample size (n = 10) and an uncontrolled design. The population was restricted to patients with metastatic prostate cancer and normal kidney function. Clinical efficacy, tumor response, and adverse clinical outcomes were not reported in the abstract.

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