4.7 Article

Quantitative determination of dithiocarbamates in human plasma, serum, erythrocytes and urine: pharmacokinetics of broccoli sprout isothiocyanates in humans

Journal

CLINICA CHIMICA ACTA
Volume 316, Issue 1-2, Pages 43-53

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/S0009-8981(01)00727-6

Keywords

isothiocyanates; dithiocarbamates; sulforaphane; glucosinolates; myrosinase; pharmacokinetics; broccoli sprouts

Funding

  1. NCI NIH HHS [P01 CA 44530] Funding Source: Medline
  2. NCRR NIH HHS [RR 00052] Funding Source: Medline

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Background: Humans are exposed to substantial quantities of isothiocyanates and glucosinolates from vegetables. Since dietary isothiocyanates are widely regarded as potentially important chemoprotectors against cancer, reliable methods for measuring the plasma and tissue pharmacokinetics of isothiocyanates and their dithiocarbamate metabolites are essential for defining dosing regimens. Methods: Isothiocyanates (ITC) and dithiocarbamates (DTC) react quantitatively with 1,2-benzenedithiol to produce 1,3-benzodithiole-2-thione that can be quantified spectroscopically. Although this cyclocondensation reaction has been highly useful for analyzing plant material and urine samples, the determination of DTC/ITC (the total quantity of DTC and ITC components in a sample that react in the cyclocondensation reaction) in blood and tissues has been hampered by their low levels and the high concentrations of proteins that interfere with the cyclocondensation reaction. The protein content of blood and tissues was reduced by the precipitation with polyethylene glycol (PEG) or ultrafiltration, and the sensitivity of the method was increased substantially by the solid phase extraction of the cyclocondensation product. Results: Pharmacokinetic measurements were made in four human volunteers who received single doses of about 200 mumol of broccoli sprout isothiocyanates (largely sulforaphane, with lesser amounts of iberin and erucin). Isothiocyanates were absorbed rapidly, reached peak concentrations of 0.943-2.27 mumol/l in plasma, serum and erythrocytes at 1 h after feeding and declined with first-order kinetics (half-life of 1.77 +/- 0.13 h). The cumulative excretion at 8 It was 58.3 +/- 2.8% of the dose. Clearance was 369 +/- 53 ml/min, indicating active renal tubular secretion. Conclusion: A sensitive and specific method for quantifying DTC levels in human plasma, serum, and erythrocytes has been devised. Determinations of ITC/DTC levels are important because: (i) dietary isothiocyanates are of potential value in reducing the risk of cancer, and (ii) humans are extensively exposed to DTC as fungicides, insecticides, pesticides and rubber vulcanization accelerators. (C) 2002 Elsevier Science B.V. All rights reserved.

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