Chang Zhi-Qiang, Li Zhao-Xin, Li Jing-Bao, Wang Ying-Zi, Li Jian
Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, No. 106 Nanjing Road, Qingdao, 266071, People's Republic of China,
Fish Physiol Biochem. 2014 Aug;40(4):1275-9. doi: 10.1007/s10695-014-9922-y. Epub 2014 Feb 28.
The pharmacokinetic profiles of sulfamonomethoxine (SMM) were investigated in flatfish tongue soles in the present study. After a single injection of SMM (40 mg/kg BW) to caudal vein of tongue sole at 20 °C, plasma drug concentration versus time data were best fitted to a three-compartment model, characterized with 0.2, 5.7, and 80.4 h for the half-life (t 1/2) of fast distribution, slow distribution, and elimination, respectively. The apparent volume of distribution was 0.1 L/kg, and the body clearance was 0.03 L/h/kg. After oral administration of SMM (200 mg/kg BW) to tongue soles at 20 °C, plasma drug concentrations were best fitted to a two-compartment model, of which the mean half-life of absorption (t 1/2ka) and elimination (t 1/2β ) were 1.7 and 95.7 h, respectively. The maximal absorption concentration (C max) was estimated as 58 mg/L at 2.5 h, and the mean systemic bioavailability (F) was 39.5 % in tongue soles after oral administration.
本研究考察了磺胺间甲氧嘧啶(SMM)在舌鳎中的药代动力学特征。在20℃条件下,向舌鳎尾静脉单次注射SMM(40mg/kg体重)后,血浆药物浓度-时间数据最佳拟合为三室模型,快速分布、缓慢分布和消除的半衰期(t1/2)分别为0.2、5.7和80.4小时。表观分布容积为0.1L/kg,机体清除率为0.03L/(h·kg)。在20℃条件下给舌鳎口服SMM(200mg/kg体重)后,血浆药物浓度最佳拟合为二室模型,其中吸收半衰期(t1/2ka)和消除半衰期(t1/2β)分别为1.7和95.7小时。给药后2.5小时的最大吸收浓度(Cmax)估计为58mg/L,口服给药后舌鳎的平均全身生物利用度(F)为39.5%。