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. 2014 Jun 6;9(6):e97885. doi: 10.1371/journal.pone.0097885

Table 2. Propranolol pharmacokinetic data.

Subject Intravenous Oral
Dose Cmax Tmax AUC0–∞ Cl Vd T1/2 Dose Cmax Tmax AUC0–∞ T1/2 F (%)
(mg) (ng×ml−1) (min) (ng×min ×ml−1) (ml×min−1) (l×kg−1) (min) (mg) (ng×ml−1) (min) (ng×min×ml−1) (min)
Patient 1 1.0 2.3 10 889 1125 8.1 293 40 90 120 39289 346 111
Patient 2 1.0 18.7 5 1818 550 5.0 477 40 59 90 48787 800 67
Patient 3 1.0 10.0 10 1310 763 5.0 257 40 52 480 55299 627 106
Patient 4 1.0 2.4 10 3029 330 5.2 824 40 156 180 143176 711 118
Patient 5 1.0 6.3 10 883 1133 13.4 485 40 25 90 22707 958 64
Patient 6 1.0 12.1 5 791 1265 9.3 358 40 50 90 14143 346 45
Patient 7 1.0 7.0 5 1752 571 4.9 504 40 63 180 72859 1029 104
Patient 8 1.0 7.4 5 7200 139 4.8 1718 40 62 180 88124 1237 31
Patient 9 1.0 2.2 10 1264 791 7.2 569 40 33 300 49476 1096 98
Patient 10 1.0 8.4 5 1432 698 10.0 934 40 20 60 17894 1362 31
Patient 11 1.0 10.6 5 1536 651 9.1 888 40 132 180 76244 838 124
Patient 12 1.2 5.9 10 1964¥ 606¥ 11.6 913 40 32 60 66527 1643 84
Patient 13 1.0 2.2 5 2540 394 8.2 934 40 53 180 42261 523 42
Patient 14 1.0 11.8 5 1004 996 4.9 275 40 82 60 44270 801 110
Patient 15 1.0 7.3 5 505 1981 8.2 193 40 59 60 23729 342 117
Summary statistics 7.6±1.1 5 1778±441 833±120 7.7±0.7* 641±100** 65±9 120 47260±5900* 844±96* 83±8*
Control 1 1.0 7.2 10 785 1273 5.7 230 40 9 90 1332 85 4
Control 2 1.0 8.9 5 1469 681 2.6 198 40 22 180 8035 165 14
Control 3 1.0 14.1 5 856 1169 4.1 158 40 60 120 15816 176 46
Control 4 1.0 13.3 5 491 2038 3.4 90 40 30 180 9978 334 51
Control 5 1.0 18.1 5 1295 772 6.1 347 40 21 180 9471 310 18
Summary statistics 12.3±2 5 979±177 1187±241 4.4±0.7 205±43 28±9 180 8930±2320 214±47 27±9.2

Abbreviations: AUC = area under the concentration-time curve; Cl = clearance; Cmax = peak concentration, Cmin = trough concentration, F = oral bioavailability, T1/2 = elimination half-life; Tmax = time point of Cmax; Vd = volume of distribution, NA = not available. Data are summarised as mean ± standard error of the mean or median as appropriate.

Case excluded from AUC and Cl statistics due to the effect of concomitant treatment with ciprofloxacin (see main body of text for mechanistic explanation),

*p<0.01 vs. control subjects,

**p<0.05 vs. control subjects,

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corrected for dose.