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. 2016 Apr 7;82(1):83–91. doi: 10.1111/bcp.12917

Table 2.

Kinetic disposition of the l‐ and d‐ nebivolol enantiomers in the investigated patients (n = 43) following a single oral dose of 10 mg racemic nebivolol. Data are expressed as geometric mean (coefficient of variation)

l‐nebivolol d‐nebivolol
Parameters Control (n = 22) CKD (n = 12) Haemodialysis (n = 10) Control (n = 22) CKD (n = 12) Haemodialysis (n = 10)
C max (ng ml –1 ) 1.31 (47) 1.98 (47) 1.38 (39) 0.69 (45)* 1.34 (54)* 0.80 (44)*
t max (h) 1.01 (0.18–2.10) 1.04 (0.68–2.80) 1.15 (0.27–1.54) 1.03 (0.43–2.14) 0.98 (0.61–3.34) 1.13 (0.40–1.86)
AUC 0–∞ (ng.h ml –1 ) 6.83 (39) 9.94 (44) 6.41 (35) 4.15 (41)* 7.30 (51)* 4.95 (36)*
t½ (h) 13.79 (35) 12.43 (35) 12.87 (27) 13.19 (47) 11.57 (30) 16.10 (31)
Vd/F (l kg –1 ) 100.19 (66) 59.38 (65) 113.70 (70) 157.60 (83)* 71.95 (64)* 197.49 (65)*
CL/F (l h –1 kg –1 ) 10.24 (47) 7.18 (32) 12.45 (35) 16.84 (41)* 9.77 (51)* 15.86 (33)*

AUC0–∞, area under the concentration–time curve from time zero extrapolated to infinity; CKD, chronic kidney disease; C max, maximal plasma concentration; CV, coefficient of variation; CL/F, oral clearance; t½, terminal elimination half‐life; t max, time to reach C max; Vd/F, apparent volume of distribution.

*

Paired t‐test, P < 0.05 (l‐nebivolol vs. d‐nebivolol);

median (range).