TY - JOUR
T1 - Influence of food on the bioavailability of oral methotrexate in children
AU - Dupuis, L. L.
AU - Koren, G.
AU - Silverman, E. D.
AU - Laxer, R. M.
PY - 1995
Y1 - 1995
N2 - Objective. To determine the bioavailability of oral methotrexate (MTX) in patients with juvenile rheumatoid arthritis in the fasting and fed states. Methods. Each patient randomly received their usual weekly MTX dose either orally (po) after an overnight fast, po immediately after a breakfast of their choice, or intravenously (iv) on 3 consecutive weeks. Blood samples were taken at 0, 0.5, 1, 1.5, 2, 3, 4, and 6 h after po and 0, 0.08, 0.25, 0.5, 1, 1.5, 2, 3, 4, and 6 h after iv administration. Results. Fourteen patients (10 female) aged 2.8 to 15.1 yrs completed the study; the results of 13 patients were evaluable. The mean elimination rate constant was 0.27 ± 0.065, 0.26 ± 0.067, and 0.25 ± 0.11 h-1 after po fasting, po fed, and iv administration, respectively. The total area under the serum concentration vs time curve was 1.87 ± 0.83, 1.50 ± 0.51, and 1.85 ± 0.80 μmol/l·h after po fasting, po fed, and iv administration, respectively. The maximum serum MTX concentration (C(max)) was 0.65 ± 0.33 and 0.39 ± 0.18 μmol/l after po fasting and po fed administration, respectively (p = 0.0022). The time to C(max) was 0.94 ± 0.40 and 1.32 ± 0.68 h after po fasting and po fed administration, respectively (p = 0.1464). The bioavailability of oral MTX while fasting was 1.1 ± 0.51, while that after a meal was 0.88 ± 0.35 (p = 0.0211). Conclusion. These data indicate greater oral bioavailability of MTX in the fasting state. We recommend that children receive MTX on an empty stomach.
AB - Objective. To determine the bioavailability of oral methotrexate (MTX) in patients with juvenile rheumatoid arthritis in the fasting and fed states. Methods. Each patient randomly received their usual weekly MTX dose either orally (po) after an overnight fast, po immediately after a breakfast of their choice, or intravenously (iv) on 3 consecutive weeks. Blood samples were taken at 0, 0.5, 1, 1.5, 2, 3, 4, and 6 h after po and 0, 0.08, 0.25, 0.5, 1, 1.5, 2, 3, 4, and 6 h after iv administration. Results. Fourteen patients (10 female) aged 2.8 to 15.1 yrs completed the study; the results of 13 patients were evaluable. The mean elimination rate constant was 0.27 ± 0.065, 0.26 ± 0.067, and 0.25 ± 0.11 h-1 after po fasting, po fed, and iv administration, respectively. The total area under the serum concentration vs time curve was 1.87 ± 0.83, 1.50 ± 0.51, and 1.85 ± 0.80 μmol/l·h after po fasting, po fed, and iv administration, respectively. The maximum serum MTX concentration (C(max)) was 0.65 ± 0.33 and 0.39 ± 0.18 μmol/l after po fasting and po fed administration, respectively (p = 0.0022). The time to C(max) was 0.94 ± 0.40 and 1.32 ± 0.68 h after po fasting and po fed administration, respectively (p = 0.1464). The bioavailability of oral MTX while fasting was 1.1 ± 0.51, while that after a meal was 0.88 ± 0.35 (p = 0.0211). Conclusion. These data indicate greater oral bioavailability of MTX in the fasting state. We recommend that children receive MTX on an empty stomach.
KW - Bioavailability
KW - Methotrexate
UR - http://www.scopus.com/inward/record.url?scp=0029120783&partnerID=8YFLogxK
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C2 - 7473485
AN - SCOPUS:0029120783
SN - 0315-162X
VL - 22
SP - 1570
EP - 1573
JO - Journal of Rheumatology
JF - Journal of Rheumatology
IS - 8
ER -