|
|
||||||||
Clinical Chemistry, Vol 36, 870-874, Copyright © 1990 by American Association for Clinical Chemistry
GA Mills and V Walker
Clinical Biochemistry, University of Southampton, U.K.
Using gas chromatography-mass spectrometry, we investigated the urinary excretion of organic acids of 278 newborn babies in a special care unit to obtain reference data and monitor metabolism. In 101 of 584 urine samples analyzed, we found isomers of cyclohexanediol. trans-1,2- Cyclohexanediol was always most abundant, with small amounts of 1,3- and 1,4-cyclohexanediol and, sometimes, traces of cis-1,2- cyclohexanediol. Glucuronide conjugates were not detected. The probable source was the solvent cyclohexanone, which was found as a contaminant of intravenous dextrose and the parenteral feeding solution, and was also leached into the infusion fluids from the administration set. We recovered 0.89 mg (range 0.74-0.98 mg, n = 5) of cyclohexanone from 150 mL of dextrose pumped through the infusion apparatus over 24 h, the normal rate for a 1-kg premature baby. Although this is well below toxic doses reported for mature animals, more data are needed for the newborn, particularly preterm infants who have a decreased capacity for glucuronide conjugation.
The following articles in journals at HighWire Press have cited this article:
![]() |
C. S. Thompson-Torgerson, H. C. Champion, L. Santhanam, Z. L. Harris, and A. A. Shoukas Cyclohexanone contamination from extracorporeal circuits impairs cardiovascular function Am J Physiol Heart Circ Physiol, June 1, 2009; 296(6): H1926 - H1932. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. E. Vandenbroucke, B. Lucas, J. Demeester, S. C. De Smedt, and N. N. Sanders Nuclear accumulation of plasmid DNA can be enhanced by non-selective gating of the nuclear pore Nucleic Acids Res., June 21, 2007; (2007) gkm440v1. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |