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单剂量和多剂量给药方案后,磺胺二甲氧嘧啶在美国龙虾(美洲螯龙虾)中的口服生物利用度和处置情况。

Oral bioavailability and disposition of sulphadimethoxine in lobster, Homarus americanus, following single and multiple dosing regimens.

作者信息

Barron M G, James M O

机构信息

Whitney Laboratory, University of Florida, St Augustine.

出版信息

Xenobiotica. 1994 Sep;24(9):921-31. doi: 10.3109/00498259409043290.

Abstract
  1. Single and multiple oral doses of sulphadimethoxine or sodium sulphadimethoxine were administered by gavage to lobster, and sequential samples of haemolymph were taken for analysis of parent sulphadimethoxine. Single doses of sodium sulphadimethoxine were given over a dose range of 14-70 mg/kg. Five 42-mg/kg doses of sulphadimethoxine on alternate days were administered for the multiple-dose studies. Some experiments were conducted with radiolabelled (35S or 14C) sulphadimethoxine, and the tissue distribution of radioactivity was determined at different killing times. 2. Pharmacokinetic parameters were obtained by fitting sulphadimethoxine concentrations in haemolymph to a one-compartment model. Oral bioavailability at the 42-mg/kg dose, calculated from the area under the haemolymph concentration-time curve (AUC) relative to the AUC from intravascular administration, was between 47 and 52% for single or multiple doses of the free drug. The bioavailability of sodium sulphadimethoxine was dose dependent, at 97% for the 14 mg/kg dose, and 25% for the 70-mg/kg dose. The low bioavailability at the high dose probably resulted from poor absorption due to the limited solubility of sulphadimethoxine at the low pH of the lobster gastrointestinal tract. 3. Sulphadimethoxine and several polar metabolites were excreted in lobster urine. Polar metabolites were also found in the hepatopancreas and haemolymph. At least 20% of the 42-mg/kg dose was metabolized. The major vertebrate metabolite of sulphadimethoxine, N-acetylsulphadimethoxine, was a very minor metabolite in lobster. The identities of the polar metabolites were not established. 4. Elimination of sulphadimethoxine residues from muscle to < 0.1 microgram sulphadimethoxine equivalent/g tissue required 40 days after a single dose, or 44 days after the last of multiple doses. Concentrations of sulphadimethoxine residues in all other tissues were always greater than muscle concentrations. Data showed that sulphadimethoxine residues were very persistent in lobster tissues.
摘要
  1. 将磺胺二甲氧嘧啶或磺胺二甲氧嘧啶钠经口单剂量和多剂量灌胃给予龙虾,并依次采集血淋巴样本以分析母体磺胺二甲氧嘧啶。单剂量给予磺胺二甲氧嘧啶钠的剂量范围为14 - 70毫克/千克。在多剂量研究中,每隔一天给予5次42毫克/千克的磺胺二甲氧嘧啶剂量。一些实验使用放射性标记(35S或14C)的磺胺二甲氧嘧啶进行,并在不同处死时间测定放射性的组织分布。2. 通过将血淋巴中磺胺二甲氧嘧啶浓度拟合到单室模型来获得药代动力学参数。根据血淋巴浓度 - 时间曲线下面积(AUC)相对于血管内给药的AUC计算,42毫克/千克剂量下的口服生物利用度,对于单剂量或多剂量的游离药物而言,在47%至52%之间。磺胺二甲氧嘧啶钠的生物利用度呈剂量依赖性,14毫克/千克剂量时为97%,70毫克/千克剂量时为25%。高剂量时生物利用度低可能是由于龙虾胃肠道低pH值下磺胺二甲氧嘧啶溶解度有限导致吸收不良。3. 磺胺二甲氧嘧啶和几种极性代谢物在龙虾尿液中排泄。在肝胰腺和血淋巴中也发现了极性代谢物。42毫克/千克剂量中至少20%被代谢。磺胺二甲氧嘧啶在主要脊椎动物中的代谢物N - 乙酰磺胺二甲氧嘧啶,在龙虾中是一种非常次要的代谢物。极性代谢物的身份未确定。4. 单剂量后,肌肉中磺胺二甲氧嘧啶残留消除至<0.1微克磺胺二甲氧嘧啶当量/克组织需要40天,多剂量末次给药后需要44天。所有其他组织中磺胺二甲氧嘧啶残留浓度始终高于肌肉浓度。数据表明,磺胺二甲氧嘧啶残留在龙虾组织中非常持久。

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