Pharmacokinetics and acetylation of sulfamethoxazole in turbot Scophthalmus maximus after intravascular administration

被引:2
作者
Chang Zhiqiang [1 ]
Liu Fei [1 ,2 ]
Lian Chun'ang [1 ,2 ]
Zhai Qianqian [1 ]
Li Jian [1 ]
机构
[1] Chinese Acad Fishery Sci, Yellow Sea Fisheries Res Inst, Minist Agr, Key Lab Sustainable Dev Marine Fisheries, Qingdao 266071, Peoples R China
[2] Shanghai Ocean Univ, Coll Fisheries & Life Sci, Shanghai 201306, Peoples R China
基金
中国国家自然科学基金;
关键词
pharmacokinetics; acetylation; sulfamethoxazole; turbot; HYDROXY METABOLITES; SULFADIMIDINE; ANTIBIOTICS; SULFADIMETHOXINE; SULFONAMIDES; N4-ACETYL; SULPHAMONOMETHOXINE; DEACETYLATION; EXCRETION; ANIMALS;
D O I
10.1007/s00343-016-4310-3
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The pharmacokinetic profiles and sulfamethoxazole (SMX) acetylation process in turbot reared at 18 degrees C were investigated. Either SMX (parent drug) or its acetylized metabolite, N-4-acetylsulfamethoxazole (AcSMX), was administered intravascularly to turbot at a dosage of 50 mg/kg BW. Serum concentrations of the parent drug and its metabolite were both measured by HPLC, and the changes in concentration over time were analyzed in two-and non-compartment models because SMX treatment produced multiple peaks. The results demonstrated that the elimination half-life of the parent drugs, SMX and AcSMX, were 159.2 and 5.9 h, respectively. The apparent volume of distribution was 0.2 and 0.8 L/kg, and the clearance was 0.038 and 0.222 L/(h.kg), for SMX and AcSMX, respectively. SMX acetylation in turbot was 2.8%, and the deacetylation of AcSMX was 0.2%. These findings may be useful in optimizing SMX dosage regimens in turbot aquaculture.
引用
收藏
页码:789 / 794
页数:6
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