CORRECTION article

Front. Vet. Sci., 26 May 2021

Sec. Veterinary Pharmacology and Toxicology

Volume 8 - 2021 | https://doi.org/10.3389/fvets.2021.665021

Corrigendum: Comparative Pharmacokinetics of Meloxicam Between Healthy Post-partum vs. Mid-lactation Dairy Cattle

  • 1. Department of Veterinary Diagnostic and Production Animal Medicine, Iowa State University College of Veterinary Medicine, Ames, IA, United States

  • 2. Analytical Chemistry Section, Veterinary Diagnostic Laboratory, Iowa State University College of Veterinary Medicine, Ames, IA, United States

  • 3. Veterinary Pharmacotherapy and Pharmacy, Department of Population Health Sciences, Utrecht University, Utrecht, Netherlands

  • 4. Department of Anatomy and Physiology, Kansas State University College of Veterinary Medicine, Manhattan, KS, United States

  • 5. SMART Pharmacology, Department of Biomedical Sciences, Iowa State University College of Veterinary Medicine, Ames, IA, United States

In the original article, there was a mistake in the legend for Tables 2 and 4 as published. In these tables, the number of cows in each group were stated incorrectly. The correct legend appears below.

Table 4

IVMid-lactationPost-partumP-value
Cmax (μg/mL)1.22 (0.92–1.55)1.06 (0.84–1.34)0.26
Tmax (h)0.13 (0.08–0.19)0.23 (0.08–4.01)0.73
Vd (L/kg)0.29 (0.24–0.35)0.31 (0.19–0.48)0.94
CL (L/kg/h)0.03 (0.02–0.03)0.01 (0.009–0.02)0.009
AUC∞ (h x μg/mL)8.26 (6.62–10.10)16.30 (6.18–31.75)0.009
AUC%extrapolated1.65 (1.29–2.06)1.68 (−11.13–29.84)0.14
λz (h−1)0.08 (0.08–0.09)0.04 (0.03–0.07)0.006
AUMC∞ (h x μg/mL)93.33 (72.00–118.95)393.75 (115.22–3908.18)0.009
MRT∞ (h)11.30 (10.44–12.19)24.16 (12.23–85.36)0.006
T1/2 (h)8.23 (7.90–8.58)17.31 (8.59–64.05)0.006
E0.008 (0.006–0.01)0.004 (0.003–0.006)0.009

Plasma pharmacokinetic parameters for meloxicam from seven post-partum cows compared to five mid-lactation cows intravenously administered a single dose of meloxicam at 0.2 mg/kg.

Results are presented in geometric means and 95% confidence intervals. P-values are based on non-parametric Wilcoxon Rank Sums 2-sample normal approximation.

Parameters include maximum plasma concentration (Cmax), time of Cmax (Tmax), area under the curve extrapolated to infinity (AUC∞), area under the first momentum curve extrapolated to infinity (AUMC∞), area under the curve percent extrapolated (AUC%extrapolated), slope of terminal phase (λz), terminal half-life (T1/2), volume of distribution (Vd), mean residence time (MRT∞), and clearance (CL).

Table 2. Plasma concentrations (μg/mL) for meloxicam from seven post-partum cows compared to five mid-lactation cows that received intravenous administration of a single dose of meloxicam at 0.2 mg/kg. Results are presented as geometric means and 95% confidence interval.

Table 4. Plasma pharmacokinetic parameters for meloxicam from seven post-partum cows compared to five mid-lactation cows intravenously administered a single dose of meloxicam at 0.2 mg/kg. Results are presented in geometric means and 95% confidence intervals. P-values are based on non-parametric Wilcoxon Rank Sums 2-sample normal approximation.

In the original article, there was a mistake in Table 4 as published. In this table, the units for Vdshould have been L/kg. The corrected Table 4 appears below.

In the original article, there was a mistake in Table 5 as published. In this table, the units for Vz/F should have been L/kg and the values for Vz/F were incorrectly reported as mL/kg. The corrected Table 5 appears below.

Table 5

OralMid-lactationPost-partumP-value
Cmax (μg/mL)1.45 (1.12–1.88)2.61 (1.79–3.67)0.02
Tmax (h)10.48 (8.50–12.83)16.75 (12.25–22.42)0.02
Vz/F (L/kg)0.39 (0.27–0.60)0.22 (0.17–0.33)0.02
CL/F (L/kg/h)0.03 (0.02–0.04)0.01 (0.007–0.019)0.008
AUC∞ (h x μg/mL)36.01 (24.29–51.02)82.82 (50.55–126.77)0.008
AUC%extrapolated0.60 (−0.09–1.89)0.47 (0.17–0.89)0.69
λz (h−1)0.07 (0.06–0.08)0.06 (0.05–0.07)0.05
AUMC∞ (h x μg/mL)733.95 (394.66–1194.39)2287.61 (981.54–4354.35)0.008
MRT∞ (h)20.38 (17.16–24.02)27.62 (21.56–34.90)0.05
T1/2 (h)9.55 (8.26–10.99)12.28 (9.60–15.42)0.05
F (%)87.2101.6–*

Plasma pharmacokinetic parameters for meloxicam from six post-partum cows matched to mid-lactation cows orally administered a single dose of meloxicam at 1.0 mg/kg.

Results are presented in geometric means and range. P-values are based on non-parametric Wilcoxon Rank Sums 2-sample normal approximation.

Parameters include maximum plasma concentration (Cmax), time of Cmax (Tmax), area under the curve extrapolated to infinity (AUC∞), area under the curve percent extrapolated (AUC%extrapolated), area under the first momentum curve to infinity (AUMC∞), slope of terminal phase (λz), terminal half-life (T1/2), volume of distribution per fraction of drug absorbed (Vz/F), mean residence time (MRT∞), clearance per fraction of drug absorbed (CL/F), and absolute bioavailability (Fabs).

*

Statistical comparisons could not be made between treatment groups due individual animals receiving a single treatment and therefore clearance cannot be assumed to be consistent.

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Summary

Keywords

meloxicam, pharmacokinetics, post-partum, NSAID, dairy

Citation

Warner R, Ydstie JA, Wulf LW, Gehring R, Coetzee JF, Mochel JP and Gorden PJ (2021) Corrigendum: Comparative Pharmacokinetics of Meloxicam Between Healthy Post-partum vs. Mid-lactation Dairy Cattle. Front. Vet. Sci. 8:665021. doi: 10.3389/fvets.2021.665021

Received

06 February 2021

Accepted

04 May 2021

Published

26 May 2021

Volume

8 - 2021

Edited and reviewed by

Arturo Anadón, Complutense University of Madrid, Spain

Updates

Copyright

*Correspondence: Patrick J. Gorden

This article was submitted to Veterinary Pharmacology and Toxicology, a section of the journal Frontiers in Veterinary Science

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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