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新型氨基环醇抗生素硫酸曲古霉素([3H]trospectomycin sulfate)在雄性和雌性犬及兔体内的药代动力学与转归。与人类的异速生长标度关系。

Pharmacokinetics and fate of [3H]trospectomycin sulfate, a novel aminocyclitol antibiotic, in male and female dogs and rabbits. Allometric scaling with human.

作者信息

Nichols D J, Burrows M, Bye A, Constable D A, Dring L G, Jeffrey P

机构信息

Pre-Clinical Research and Development, Upjohn Laboratories (UK), Upjohn Ltd, West Sussex, England.

出版信息

Drug Metab Dispos. 1991 Jul-Aug;19(4):781-6.

PMID:1680655
Abstract

The pharmacokinetics and fate of [3H]trospectomycin sulfate, a novel aminocyclitol antibiotic, were examined in male and female dogs and rabbits. Total radioactivity levels in plasma were associated with unchanged trospectomycin in both dog and rabbit. No unchanged drug was found in rabbit urine. Two radioactive components were found in dog urine; one was indistinguishable from trospectomycin and the other was probably a degradation product. The disappearance of drug from plasma followed a biphasic pattern and was well described by a bi-exponential function with half-lives of 0.4-0.8 and 30-70 hr in the dog and 0.4 and 90-120 hr in the rabbit. There was a large distribution volume (Vss), which indicated some retention of drug by tissues. The clearance (CL) for both animals was within the normal range for glomerular filtration rate. CL and Vss were not different between the sexes in the dog or rabbit. Excretion in both animals was initially rapid (greater than 40% by 4 hr) and mainly by the urinary route (fecal excretion less than 10%). Urinary excretion was not significantly different between the sexes. Over the dose range of 25-100 mg/kg, the plasma pharmacokinetics in the dog were linear. However, the recovery of radioactivity in the urine was significantly reduced at the highest dose. Trospectomycin CL in rat, human (obtained from previous studies), dog, and rabbit was described by the allometric equation, CL (ml/hr) = 132 x M0.91 where M is the body mass in kg.

摘要

对新型氨基环醇抗生素硫酸[³H]曲古霉素在雄性和雌性犬及兔体内的药代动力学和转归进行了研究。犬和兔血浆中的总放射性水平与未变化的曲古霉素相关。兔尿中未发现未变化的药物。犬尿中发现了两种放射性成分;一种与曲古霉素无法区分,另一种可能是降解产物。药物从血浆中的消失呈双相模式,可用双指数函数很好地描述,犬的半衰期为0.4 - 0.8小时和30 - 70小时,兔的半衰期为0.4小时和90 - 120小时。分布容积(Vss)较大,表明组织对药物有一定的潴留。两种动物的清除率(CL)均在肾小球滤过率的正常范围内。犬和兔的CL和Vss在性别之间无差异。两种动物的排泄最初都很快(4小时内大于40%),主要通过尿液途径(粪便排泄小于10%)。两性之间的尿排泄无显著差异。在25 - 100 mg/kg的剂量范围内,犬的血浆药代动力学呈线性。然而,在最高剂量时,尿中放射性的回收率显著降低。大鼠、人(来自先前研究)、犬和兔的曲古霉素CL可用异速生长方程描述,CL(ml/hr)= 132 x M⁰.⁹¹,其中M是以kg为单位的体重。

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