Pharmacokinetics and bioavailability of cefuroxime in Nile tilapia (Oreochromis niloticus)
 
Yazarlar (11)
Prof. Dr. Orhan Çorum Hatay Mustafa Kemal Üniversitesi, Türkiye
Doç. Dr. Duygu Durna Çorum Hatay Mustafa Kemal Üniversitesi, Türkiye
Pedro Marin
Universidad De Murcia, İspanya
Prof. Dr. Önder Yıldırım Muğla Sıtkı Koçman Üniversitesi, Türkiye
Doç. Dr. Ertuğrul TERZİ Kastamonu Üniversitesi, Türkiye
Ruby C. Gonzales
Mindanao State University At Naawan, Filipinler
Dan M. Arrıesgado
Mindanao State University At Naawan, Filipinler
Victor R. Navarro
Mindanao State University At Naawan, Filipinler
Doç. Dr. Soner BİLEN Kastamonu Üniversitesi, Türkiye
Doç. Dr. Adem Yavuz SÖNMEZ Kastamonu Üniversitesi, Türkiye
Prof. Dr. Kamil Üney Selçuk Üniversitesi, Türkiye
Makale Türü Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı Veterinary Research Communications (Q2)
Dergi ISSN 0165-7380 Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler SCI-Expanded
Makale Dili İngilizce Basım Tarihi 11-2026
Cilt / Sayı / Sayfa 50 / 1 / 18–0 DOI 10.1007/s11259-025-10974-8
Makale Linki https://doi.org/10.1007/s11259-025-10974-8
UAK Araştırma Alanları
Su Ürünleri Yetiştiriciliği
Özet
Cefuroxime is a broad-spectrum antibiotic extensively utilized in humans and animals. Although it has been reported as beneficial against certain fish infections, pharmacokinetic studies are lacking. The purpose of this study was to evaluate the pharmacokinetics of cefuroxime following intravascular (IV, n = 72), intraperitoneal (IP, n = 72), intramuscular (IM, n = 72), and oral (n = 72) administration of 20 mg/kg in Nile tilapia (Oreochromis niloticus) maintained at 29 ± 1.5 °C. Two hundred and eighty-eight fish were equally distributed among four treatment groups: IV, IP, IM, and oral. Blood samples were obtained from 6 fish per group at 12 distinct time intervals over a duration of 96 h. Cefuroxime plasma concentrations were quantified with high-performance liquid chromatography and subsequently evaluated through non-compartmental analysis. Following IV injection, the t1/2ʎz was 8.04 h, the Vdss was 1.03 L/kg, and the ClT was 0.14 L/h/kg. The Cmax of cefuroxime was 53.38±4.28 µg/mL at 0.25 h for IP injection, 28.70±3.41 µg/mL at 0.5 h for IM injection, and 6.77±0.81 µg/mL at 1 h for oral administration. Bioavailability was 80.26% (IP), 69.05% (IM), and 24.35% (oral). This study found that a dosing interval of 24 h for IP and IM injection or 8 h for oral administration is efficient for treating bacteria with a MIC value of ≤ 1 µg/mL. The findings of this study indicate that IP and IM injections of cefuroxime are applicable in tilapia. However, since oral administration is important in aquaculture, studies are needed to develop new formulations with better absorption, to demonstrate therapeutic efficacy in infected fish, and to determine the tissues residue depletion.
Anahtar Kelimeler
Cefuroxime | Different routes | Nile tilapia | Pharmacokinetic
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Scopus 1
Pharmacokinetics and bioavailability of cefuroxime in Nile tilapia (Oreochromis niloticus)

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