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S R Bernard

Publications and source records attributed to S R Bernard.

12 recordsLinked to original sources

Gastrointestinal absorption of americium-241 by orally exposed swine: comparison of experimental results with predictions of metabolic models.

Two groups of 11-week-old swine (40 miniature and 40 domestic swine) received a single oral administration of 1.9 X 10(8) Bq (5.2 mCi) of 241Am citrate, and groups of eight animals, four of each type, were killed and sampled at 1, 2, 4, 8, 16, 24, 48, 72, and 96 h and 30 days later. Uptake and excretion patterns of the radioactivity appeared to occur in three phases: rapid uptake, rapid excretion, and then a slower excretion. All animals were systematically dissected, and the eviscerated carcasses were autoclaved for separation of bone and muscle. The predominant site of deposition was bone, and autoclaving had little effect on releasing 241Am from either bone or muscle. The maximum fractional gastrointestinal absorption of 1.1 X 10(-3) occurred 8 h after radionuclide administration. The tissue distribution data suggest partitions of 50, 20, and 30%, for bone, liver, and other soft tissues, respectively. Two metabolic models were evaluated: a modified Mewhinney-Griffith model and the ICRP 30 model to compare the biological data with model predictions. All models underestimated the actual early time data, but the fits to the experimental results were better at later times.

Administration, Oral

Metabolic models for methyl and inorganic mercury.

We have derived two different models representing the metabolic behavior of both inorganic and methyl mercury. Simple three- and four-compartment models fit the short-term data very well. However, it was necessary to add long-term compartments to the data so the model would be in keeping with the long-term data as observed in Reference Man, ICRP Publication 23 and in industrial experience (ICRP75). One concept not used in our models is biotransformation. It has been established that in the rat methyl mercury undergoes a biotransformation that cleaves the carbon-methyl bond and releases inorganic mercury (No 70; No 71). However, we were unable to find any human data. Since methylation of inorganic mercury is known to occur, it might be expected that methylation would occur in mammals. Rowland et al. have shown that the contents of the rat cecum can synthesize methyl mercury from mercuric chloride (Row 77). Furthermore, they also showed that bacteria from human feces can cause methylation. Clearly, a model incorporating biotransformation would be useful but it must await further experimental evidence.

Body Fluid Compartments