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. 2001 Nov;52(5):529–538. doi: 10.1046/j.0306-5251.2001.01493.x

Table 2.

Pharmacokinetic parameters of distribution and elimination of budesonide and fluticasone after intravenous administration of 200 µg, respectively.

Substance Subjects n Dose (nmol)* t½ (h) AUC (nmol l−1 h) MRT (h) CL (ml min−1) Vss (l)
Budesonide Healthy 13 406 (49) 4.4 (3.7; 5.4) 5.0 (4.5; 5.6) 3.5 (3.0; 4.0) 1334 (1213; 1466) 280 (245; 321)
With asthma 8 397 (24) 4.6 (3.5; 6.1) 4.9 (4.2; 5.8) 3.8 (3.1; 4.7) 1344 (1167; 1548) 310 (269; 357)
Total 21 403 (39) 4.5 (3.9; 5.2) 5.0 (4.6; 5.4) 3.6 (3.3; 4.0) 1338 (1245; 1437) 291 (265; 320)
Fluticasone Healthy 13 377 (19) 12.7 (9.4; 17.2) 5.0 (4.6; 5.5) 8.0 (5.8; 11.0) 1245 (1140; 1359) 599 (448; 800)
With asthma 8 386 (26) 12.0 (9.0; 16.1) 4.5 (3.6; 5.7) 7.1 (5.3; 9.5) 1418 (1134; 1775) 607 (475; 777)
Total 21 380 (22) 12.5 (10.2; 15.2) 4.8 (4.4; 5.3) 7.7 (6.2; 9.5) 1308 (1192; 1436) 602 (500; 726)

Values given as geometric means (95% CI).

*

Arithmetic mean (s.d.).

t½=half-life; AUC=area under the curve of plasma concentration vs time; MRT=mean residence time; CL=clearance; Vss=volume of distribution at steady state.