PHARMACOKINETICS OF METRONIDAZOLE IN GREEN (CHELONIA MYDAS), LOGGERHEAD (CARETTA CARETTA), AND KEMP'S RIDLEY (LEPIDOCHELYS KEMPII) SEA TURTLES AFTER SINGLE ORAL AND INTRAVENOUS DOSES.

IF 0.7 4区 农林科学 Q3 VETERINARY SCIENCES Journal of Zoo and Wildlife Medicine Pub Date : 2024-12-01 DOI:10.1638/2024-0012
Terry M Norton, Sherry Cox, Charles A Manire, Bette Zirkelbach, Ian Morrison, Rachel Overmeyer, Stephanie Stowell, Leah Adelman, Sarah Buttrey, Taylor Marcialis, Maximillian M R Polyak, Samantha Clark, Jamie Gamby, Allison Hardman, Isabelle Gilbert, Krista Breshears, Maria Chadam, Whitney Crowder, Emily Mirowski, Shelby Hoover, Annie Page
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Abstract

Currently there are few antibacterial dosage regimens established to be safe and effective for sea turtles. Pharmacokinetic evaluation of antibiotics is an essential step in establishing accurate dosage guidelines for a particular species. Metronidazole is an antibiotic that is effective against anaerobic bacteria and some protozoa. For most anaerobic bacteria, the minimum inhibitory concentration (MIC) for metronidazole ranges from 0.25 to 4.0 µg/ml. The MIC values for some Clostridium species are up to 8 µg/ml, and for protozoal agents of trichomoniasis (MIC of 0.05 µg/ml), amebiasis, and giardiasis the MIC ranges from 1 to 50 µg/ml. The objective of this study was to determine the pharmacokinetic parameters after administration of metronidazole to aid in the establishment of species-specific dose guidelines in green (Chelonia mydas), loggerhead (Caretta caretta), and Kemp's ridley (Lepidochelys kempii) sea turtles. After administering metronidazole at a dose of 20 mg/kg orally and IV, the pharmacokinetics were very similar for these three species of sea turtles (n = 6 for each species). For both oral and IV routes of administration, plasma metronidazole concentrations were maintained above 8 µg/ml for approximately 24 h and above 4 µg/ml for approximately 48 h; however, plasma concentrations of 8 µg/ml were reached within 5 min only for the IV route, versus 8 h for the oral route.

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单次口服和静脉注射给药后甲硝唑在绿海龟、红海龟和肯普雷氏海龟体内的药代动力学。
目前,对海龟安全有效的抗菌剂量方案很少。抗生素的药代动力学评价是为特定品种建立准确剂量指南的重要步骤。甲硝唑是一种抗生素,对厌氧菌和一些原生动物有效。对于大多数厌氧菌,甲硝唑的最低抑制浓度(MIC)范围为0.25至4.0µg/ml。一些梭状芽孢杆菌的MIC值高达8微克/毫升,而滴虫病(MIC为0.05微克/毫升)、阿米巴病和贾第虫病等原虫的MIC值在1至50微克/毫升之间。本研究的目的是测定甲硝唑给药后的药代动力学参数,以帮助绿海龟(Chelonia mydas)、红海龟(Caretta Caretta)和肯普雷氏海龟(Lepidochelys kempii)建立物种特异性剂量指南。口服和静脉注射剂量为20 mg/kg的甲硝唑后,三种海龟的药代动力学非常相似(每种n = 6)。口服和静脉给药时,血浆甲硝唑浓度维持在8µg/ml以上约24小时,维持在4µg/ml以上约48小时;然而,只有静脉给药在5分钟内达到8µg/ml的血浆浓度,而口服给药在8小时内达到8µg/ml。
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来源期刊
Journal of Zoo and Wildlife Medicine
Journal of Zoo and Wildlife Medicine 农林科学-兽医学
CiteScore
1.70
自引率
14.30%
发文量
74
审稿时长
9-24 weeks
期刊介绍: The Journal of Zoo and Wildlife Medicine (JZWM) is considered one of the major sources of information on the biology and veterinary aspects in the field. It stems from the founding premise of AAZV to share zoo animal medicine experiences. The Journal evolved from the long history of members producing case reports and the increased publication of free-ranging wildlife papers. The Journal accepts manuscripts of original research findings, case reports in the field of veterinary medicine dealing with captive and free-ranging wild animals, brief communications regarding clinical or research observations that may warrant publication. It also publishes and encourages submission of relevant editorials, reviews, special reports, clinical challenges, abstracts of selected articles and book reviews. The Journal is published quarterly, is peer reviewed, is indexed by the major abstracting services, and is international in scope and distribution. Areas of interest include clinical medicine, surgery, anatomy, radiology, physiology, reproduction, nutrition, parasitology, microbiology, immunology, pathology (including infectious diseases and clinical pathology), toxicology, pharmacology, and epidemiology.
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