Pharmacokinetic profile of amoxicillin and its glucuronide‐like metabolite when administered subcutaneously to koalas ( Phascolarctos cinereus)
Abstract Amoxicillin was administered as a single subcutaneous injection at 12.5 mg/kg to four koalas and changes in amoxicillin plasma concentrations over 24 hr were quantified. Amoxicillin had a relatively low average ± SD maximum plasma concentration ( C max) of 1.72 ± 0.47 µg/ml; at an average ± SD time to reach C max( T max) of 2.25 ± 1.26 hr, and an elimination half‐life of 4.38 ± 2.40 hr. The pharmacokinetic profile indicated relatively poor subcutaneous absorption. A metabolite was also identified, likely associated with glucuronic acid conjugation. Bacterial growth inhibition assays demonstrated that all plasma samples other than t = 0 hr, inhibited the growth of Escherichia coli ATCC 25922 and Staphylococcus aureus ATCC 29213 to some extent. Calculated pharmacokinetic indices were used to predict whether this dose could attain a plasma concentration to inhibit some susceptible Gram‐negative and Gram‐positive pathogens. It was predicted that a twice daily dose of 12.5 mg/kg would be efficacious to inhibit susceptible bacteria with an amoxicillin minimum inhibitory concentration (MIC) ≤ 0.75 µg/ml such as susceptible Bordetella bronchiseptica, E. coli, Staphylococcus spp. and Streptococcus spp. pathogens..
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2020 |
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Erschienen: |
2020 |
Enthalten in: |
Zur Gesamtaufnahme - volume:43 |
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Enthalten in: |
Journal of Veterinary Pharmacology and Therapeutics - 43(2020), 2, Seite 115-122 |
Beteiligte Personen: |
Kimble, Benjamin [VerfasserIn] |
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BKL: |
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Anmerkungen: |
Copyright 2020 John Wiley & Sons Ltd |
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Umfang: |
8 |
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doi: |
10.1111/jvp.12767 |
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funding: |
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PPN (Katalog-ID): |
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520 | |a Abstract Amoxicillin was administered as a single subcutaneous injection at 12.5 mg/kg to four koalas and changes in amoxicillin plasma concentrations over 24 hr were quantified. Amoxicillin had a relatively low average ± SD maximum plasma concentration ( C max) of 1.72 ± 0.47 µg/ml; at an average ± SD time to reach C max( T max) of 2.25 ± 1.26 hr, and an elimination half‐life of 4.38 ± 2.40 hr. The pharmacokinetic profile indicated relatively poor subcutaneous absorption. A metabolite was also identified, likely associated with glucuronic acid conjugation. Bacterial growth inhibition assays demonstrated that all plasma samples other than t = 0 hr, inhibited the growth of Escherichia coli ATCC 25922 and Staphylococcus aureus ATCC 29213 to some extent. Calculated pharmacokinetic indices were used to predict whether this dose could attain a plasma concentration to inhibit some susceptible Gram‐negative and Gram‐positive pathogens. It was predicted that a twice daily dose of 12.5 mg/kg would be efficacious to inhibit susceptible bacteria with an amoxicillin minimum inhibitory concentration (MIC) ≤ 0.75 µg/ml such as susceptible Bordetella bronchiseptica, E. coli, Staphylococcus spp. and Streptococcus spp. pathogens. | ||
700 | 1 | |a Vogelnest, Larry |4 aut | |
700 | 1 | |a Gharibi, Soraya |4 aut | |
700 | 1 | |a Izes, Aaron M. |4 aut | |
700 | 1 | |a Govendir, Merran |4 aut | |
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