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Pharmacokinetics of tolfenamic acid in Hawksbill turtles ( Eretmochelys imbricata ) after single intravenous and intramuscular administration
Author(s) -
Raweewan Natsuda,
Laovechprasit Weerapong,
Giorgi Mario,
Chomcheun Thanaphan,
Klangkaew Narumol,
Imsilp Kanjana,
Poapolathep Amnart,
Poapolathep Saranya
Publication year - 2020
Publication title -
journal of veterinary pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.527
H-Index - 60
eISSN - 1365-2885
pISSN - 0140-7783
DOI - 10.1111/jvp.12823
Subject(s) - pharmacokinetics , bioavailability , dose , pharmacology , intramuscular injection , plasma concentration , body weight , half life , medicine , chemistry
To the best of our knowledge, limited pharmacokinetic information to establish suitable therapeutic plans is available for Hawksbill turtles. Therefore, the present study aimed to assess the pharmacokinetic features of tolfenamic acid (TA) in Hawksbill turtles, Eretmochelys imbricata, after single intravenous (i.v.) and intramuscular (i.m.) administration at dosage 4 mg/kg body weight (b.w.). The study (parallel design) used 10 Hawksbill turtles randomly divided into equal groups. Blood samples were collected at assigned times up to 144 hr. The concentrations of TA in plasma were quantified by a validated liquid chromatography tandem mass spectrometry (LC‐ESI‐MS/MS). The concentration of TA in the experimental turtles with respect to time was pharmacokinetically analyzed using a noncompartment model. The C max values of TA were 89.33 ± 6.99 µg/ml following i.m. administration. The elimination half‐life values were 38.92 ± 6.31 hr and 41.09 ± 9.32 hr after i.v. and i.m. administration, respectively. The absolute i.m. bioavailability was 94.46%, and the average binding percentage of TA to plasma protein was 31.39%. TA demonstrated a long half‐life and high bioavailability following i.m. administration. Therefore, the i.m. administration is recommended for use in clinical practice because it is both easier to perform and provides similar plasma concentrations to the i.v. administration. However, further studies are needed to determine the clinical efficacy of TA for treatment of inflammatory disease after single and multiple dosages.