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复方磺胺甲噁唑在鲫鱼体内的药代动力学研究
韩 冰1,2, 杨洪波1,2, 王 荻,等1
1.中国水产科学研究院 黑龙江水产研究所;2.上海海洋大学 水产与生命学院
摘要:
【目的】研究复方磺胺甲噁唑在鲫鱼体内的药物代谢动力学(以下简称药动学)特征,为制定其合理的用药方案提供理论依据。【方法】对体质量为(68.18±14.68) g/尾的鲫鱼以500 mg/kg的剂量单次口灌复方磺胺甲噁唑粉(100 g含磺胺甲噁唑(SMZ)8.33 g、甲氧苄啶(TMP) 1.67 g)混悬液,并分别于给药后0.25,0.5,0.75,1,1.5,2,4,6,8,12,24,36,48,72 h采集鲫鱼血浆、肌肉、肝和肾4种组织,采用高效液相色谱 紫外检测法(HPLC-UV)对样品进行检测,通过3p97软件分析药动学参数。【结果】甲氧苄啶在鲫鱼血浆、肌肉和肾中的药动学特征符合一级吸收二室开放模型,在肝中的药动学特征符合一级吸收一室开放模型;磺胺甲噁唑在鲫鱼血浆、肌肉、肝和肾中的药动学特征符合一级吸收二室开放模型。【结论】药物的2种主要成分在健康鲫鱼体内吸收较完全,分布广泛,甲氧苄啶较磺胺甲噁唑吸收快、消除慢。
关键词:  高效液相色谱-紫外检测法  复方磺胺甲噁唑  鲫鱼  药物代谢动力学
DOI:
分类号:
基金项目:公益性行业(农业)科研专项(201203085);现代农业产业技术体系建设专项(CARS-46)
Pharmacokinetics of compound sulfamethoxazole in crucian carp
HAN Bing,YANG Hong-bo,WANG Di,et al
Abstract:
【Objective】This paper studied the pharmacokinetics of compound sulfamethoxazole in crucian carp(Carassius auratus) to provide theoretical basis for designing reasonable medication scheme.【Method】After oral administration of compound sulfamethoxazole (100 g containing 8.33 g SMZ and 1.67 g TMP) suspension liquid with a dosage of 500 mg/kg to crucian carps with weight of (68.18±14.68) g,plasma,muscle,liver and kidney samples were collected at 0.25,0.5,0.75,1,1.5,2,4,6,8,12,24,36,48,and 72 h,respectively.The samples were measured by high performance liquid chromatography-ultraviolet method (HPLC-UV) and the pharmacokinetic parameters were obtained by 3p97 software.【Result】The pharmacokinetics of trimethoprim(TMP) in plasma,muscle,and kidney were in line with the two-compartment open model with first-order absorption and the pharmacokinetics in liver was best described by one-department open model with first-order absorption.The pharmacokinetics of sulfamethoxazole (SMZ) in plasma,muscle,liver and kidney were best described by the two-compartment open model with first-order absorption.【Conclusion】The two main components of compound sulfamethoxazole were well absorbed and widely distributed.TMP was absorbed more rapidly and eliminated more slowly than SMZ.
Key words:  HPLC-UV  compound sulfamethoxazole  crucian carp  pharmacokinetic