Erratum to “Comparative Pharmacokinetics of Levofloxacin in Healthy and Renal Damaged Muscovy Ducks following Intravenous and Oral Administration”

Table 2

Pharmacokinetic parameters of levofloxacin in healthy and renal damaged ducks after a single PO administration of 10 mg kg⁻¹ bwt (𝑛=6).

Parameter	Unit	Healthy	Renal damaged
𝐾ab	h^−1	3.31±0.10	0.47±0.07^∗∗∗
𝐾el	h^−1	0.24±0.02	0.18±0.01^∗
𝑡1/2(ab)	h	0.22±0.01	1.45±0.08^∗∗∗
𝑡1/2(el)	h	2.89±0.09	3.94±0.14^∗∗∗
𝐶max	𝜇g mL^−1	3.63±0.12	4.05±0.13
𝑡max	h	2.05±0.08	2.47±0.11^∗
AUC	𝜇g mL^−1h^−1	17.97±2.24	37.38±2.28^∗∗∗
AUMC	𝜇g mL^−1h^−2	73.46±2.61	255.49±17.59^∗∗∗
MRT	h	4.08±0.14	6.83±0.19^∗∗∗
MAT	h	0.74±0.08	0.70±0.07
F	%	73.56±2.38	71.88±2.42
𝐶max/MIC	Ratio	36.29±2.44	40.52±2.47
AUC/MIC	Ratio	179.72±11.35	373.81±21.03^∗∗∗

^∗𝑃<0.05, ^∗∗∗𝑃<0.001 refers to degree of significance.
𝑘_ab: first-order absorption rate constant; 𝐾_el: elimination rate constant; 𝑡_1/2(ab): absorption half-life; 𝑡_1/2(el): elimination half-life; 𝐶_max: maximum plasma concentration; 𝑡_max: time to peak plasma concentration; MAT: mean absorption time; F: fraction of drug absorbed systemically after PO administration; 𝐶_max/MIC: maximum serum concentration/minimum inhibitory concentration ratio; AUC/MIC: area under concentration-time curve/MIC ratio.