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Chromatographic Separation and Characterization of LinkageIsomers of the 3-(Pyridin-2-yl)-l//-l,2,4-triazole Complex of Ruthenium(II) Bis(2,2-bipyridyl)

Pyridin-2'-yl)-l,2,4-triazoles. X-Ray Crystal Structure of Bis(2,2'-bipyridine)-[3-methyl-5-( pyridin-2'-yl)-I ,2,4-triazolato-N1] ruthenium

Development of supplementation guidelines for formulated diets and total parenteral nutrition requires knowledge of Se tissue accretion. To this end, the total organ Se content was calculated from the Se concentrations that were measured by neutron activation analysis in postmortem samples of liver (n=56), kidney (n=11), adrenal cortex (n=9), and pancreas (n=6) from infants and children from birth to 10 yr including 17 born prematurely. Hepatic Se concentrations were similar in full-term and premature newborns, decreased from birth to 1 yr, and then increased thereafter. The total hepatic Se content was significantly greater in full-term than in preterm newborns and increased with age and liver size after 1 yr. No significant differences were found between the concentrations of Se in kidney, pancreas, and adrenal tissues. Falling hepatic Se concentrations in the full-term infant concurrent with stable total organ Se content may indicate inadequate dietary intake or may reflect a normal redistribution of the nutrient. Premature infants are born with smaller stores than full-term infants and are at greater risk of developing a deficiency.