TY - JOUR
T1 - Efficacy of orally administered deferoxamine, activated charcoal, and sodium bicarbonate in acute iron intoxication in rats
T2 - Implications for the treatment of pediatric iron poisoning
AU - Eshel, Gideon
AU - Barr, Joseph
AU - Chazan, Shlomo
AU - Tavori, Irit
AU - Kariv, Noam
AU - Schejter, Abel
AU - Greenberg, Revital
AU - Berkovitch, Matitiahu
PY - 2000
Y1 - 2000
N2 - Background: Iron supplements are the most frequent cause of pediatric fatalities from unintentional ingestion. The ability to prevent iron absorption from the digestive tract is limited. Although activated charcoal (AC) alone does not absorb iron, the oral administration of deferoxamine (DFO) and AC has been shown to reduce iron absorption in human volunteers. In the presence of sodium bicarbonate (NaHCO3), ferrous iron is oxidized to ferric iron. Therefore, the coadministration of DFO, AC, and NaHCO3 may enhance enteral iron chelation. Objective: The purpose of the study was to determine whether the oral administration of DFO and AC, with or without NaHCO3, can reduce iron absorption from the digestive tract. Methods: In a rat model of acute iron overloading, ferrous sulfate (FeSO4) 100 mg/kg body weight was administered by garage, followed by DFO 150 mg/kg, AC 500 mg/kg, and NaHCO3 1 mEq/kg. Results: The administration of FeSO4 100 mg/kg increased serum iron concentrations to >350 μg/100 mL. Oral dosing with DFO and AC (separately and simultaneously, immediately or after 10 to 20 minutes) did not prevent iron absorption from the digestive tract. Subsequently, however, DFO significantly decreased the elcrated serum iron concentrations (P < 0.05), probably by chelating the already absorbed iron. Coadministration of NaHCO3 further decreased (P < 0.01) the serum iron concentration. Conclusions: Although orally administered DFO and AC do not prevent iron absorption from the digestive tract, DFO does increase the rate of iron excretion from the body, and NaHCO3 enhances this effect.
AB - Background: Iron supplements are the most frequent cause of pediatric fatalities from unintentional ingestion. The ability to prevent iron absorption from the digestive tract is limited. Although activated charcoal (AC) alone does not absorb iron, the oral administration of deferoxamine (DFO) and AC has been shown to reduce iron absorption in human volunteers. In the presence of sodium bicarbonate (NaHCO3), ferrous iron is oxidized to ferric iron. Therefore, the coadministration of DFO, AC, and NaHCO3 may enhance enteral iron chelation. Objective: The purpose of the study was to determine whether the oral administration of DFO and AC, with or without NaHCO3, can reduce iron absorption from the digestive tract. Methods: In a rat model of acute iron overloading, ferrous sulfate (FeSO4) 100 mg/kg body weight was administered by garage, followed by DFO 150 mg/kg, AC 500 mg/kg, and NaHCO3 1 mEq/kg. Results: The administration of FeSO4 100 mg/kg increased serum iron concentrations to >350 μg/100 mL. Oral dosing with DFO and AC (separately and simultaneously, immediately or after 10 to 20 minutes) did not prevent iron absorption from the digestive tract. Subsequently, however, DFO significantly decreased the elcrated serum iron concentrations (P < 0.05), probably by chelating the already absorbed iron. Coadministration of NaHCO3 further decreased (P < 0.01) the serum iron concentration. Conclusions: Although orally administered DFO and AC do not prevent iron absorption from the digestive tract, DFO does increase the rate of iron excretion from the body, and NaHCO3 enhances this effect.
KW - Activated charcoal
KW - Deferoxamine
KW - Iron intoxication
KW - Sodium bicarbonate
UR - http://www.scopus.com/inward/record.url?scp=0033827596&partnerID=8YFLogxK
U2 - 10.1016/S0011-393X(00)88016-9
DO - 10.1016/S0011-393X(00)88016-9
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AN - SCOPUS:0033827596
SN - 0011-393X
VL - 61
SP - 648
EP - 656
JO - Current Therapeutic Research - Clinical and Experimental
JF - Current Therapeutic Research - Clinical and Experimental
IS - 9
ER -