Tardieu Didier, Bailly Jean-Denis, Skiba Fabien, Grosjean François, Guerre Philippe
ENVT, Mycotoxicology Unit, 31076 Toulouse Cedex 3, France.
Food Chem Toxicol. 2008 Sep;46(9):3213-8. doi: 10.1016/j.fct.2008.07.013. Epub 2008 Jul 25.
The kinetic of fumonisin B1 (FB1) after a single IV and oral dose, and FB1 persistence in tissue were investigated in turkey poults by HPLC after purification of samples on columns. After IV administration (single-dose: 10mg FB1/kg bw), serum concentration-time curves were best described by a three-compartment open model. Elimination half-life and mean residence time of FB1 were 85 and 52min, respectively. After oral administration (single-dose: 100mg FB1/kg bw) bioavailability was 3.2%; elimination half-life and mean residence time were 214 and 408min, respectively. Clearance of FB1 was 7.6 and 7.5ml/min/kg for IV and oral administration, respectively. Twenty-four hours after the administration of FB1 by the intravenous route, liver and kidney contained the highest levels of FB1 in tissues, level in muscle was low or below the limit of detection (LD, 13microg/kg). The persistence of FB1 in tissue was also studied after administration for 9 weeks of a feed that contained 5, 10 and 20mg FB1+FB2/kg diet. Eight hours after the last intake of 20mg FB1+FB2/kg feed (maximum recommended concentration of fumonisins established by the EU for avian feed), hepatic and renal FB1 concentrations were 119 and 22microg/kg, level in muscles was below the LD.
通过柱上样品纯化后采用高效液相色谱法(HPLC),研究了火鸡雏单次静脉注射和口服伏马毒素B1(FB1)后的动力学以及FB1在组织中的持久性。静脉注射(单剂量:10mg FB1/kg体重)后,血清浓度-时间曲线最适合用三室开放模型描述。FB1的消除半衰期和平均驻留时间分别为85分钟和52分钟。口服给药(单剂量:100mg FB1/kg体重)后,生物利用度为3.2%;消除半衰期和平均驻留时间分别为214分钟和408分钟。静脉注射和口服给药时,FB1的清除率分别为7.6和7.5ml/分钟/千克。静脉注射FB1 24小时后,肝脏和肾脏在组织中所含FB1水平最高,肌肉中的水平较低或低于检测限(LD,13μg/kg)。在含有5、10和20mg FB1+FB2/千克日粮的饲料喂养9周后,也研究了FB1在组织中的持久性。在最后一次摄入20mg FB1+FB2/千克饲料(欧盟规定的禽饲料中伏马毒素的最大推荐浓度)8小时后,肝脏和肾脏中FB1浓度分别为119和22μg/kg,肌肉中的水平低于检测限。