Pepin S, Lutsch C, Grandgeorge M, Scherrmann J M
Institut National de la Santé et de la Recherche Médicale, U26, Hôpital Fernand Widal, Paris, France.
Pharm Res. 1995 Oct;12(10):1470-3. doi: 10.1023/a:1016279219619.
The pharmacokinetics of a currently available horse F(ab')2 antivenoms to Vipera aspis, V. ammodytes, and V. berus (Ipser Europe) and a new more purified and pasteurized preparation (SAV) was investigated in the rabbit.
An immunoradiometric assay using an affinity-purified goat IgG horse F(ab')2 specific and the same IgG labelled with iodine 125 as a tracer was developed. The limit of quantification in plasma was 0.032 microgram/ml. Specificity study showed that mouse F(ab')2 and Fab did not cross-react.
Pharmacokinetic analysis showed that the plasma F(ab')2 concentration followed a biexponential decline after intravenous bolus administration with distribution and elimination half-lives of 2.66 +/- 0.18 hrs and 49.69 +/- 4.13 hrs, respectively. The total volume of distribution (Vdss or Vd beta) was between 209 and 265 ml.kg-1 and was similar to the volume of the extracellular fluid in the rabbit (300 ml.kg-1). Total body clearance ranged from 3.33 to 3.96 ml.h-1.kg-1. After intramuscular administration which was only investigated with SAV, Tmax was 48 hrs and the absolute bioavailability was 42%.
No difference in pharmacokinetics was observed between the two antivenom preparations following the intravenous administration. In contrast, a reduced rate and extent of absorption was shown following intramuscular administration.
在兔体内研究了目前市售的针对极北蝰、角蝰和蝰蛇(Ipser Europe)的马F(ab')2抗蛇毒血清以及一种新的更纯化和巴氏消毒制剂(SAV)的药代动力学。
开发了一种免疫放射分析方法,使用亲和纯化的山羊抗马F(ab')2 IgG特异性抗体以及用碘125标记的相同IgG作为示踪剂。血浆中的定量限为0.032微克/毫升。特异性研究表明,小鼠F(ab')2和Fab不发生交叉反应。
药代动力学分析表明,静脉推注给药后,血浆F(ab')2浓度呈双指数下降,分布半衰期和消除半衰期分别为2.66±0.18小时和49.69±4.13小时。分布总体积(Vdss或Vdβ)在209至265毫升·千克-1之间,与兔的细胞外液体积(300毫升·千克-1)相似。全身清除率范围为3.33至3.96毫升·小时-1·千克-1。仅对SAV进行了肌肉注射给药研究,Tmax为48小时,绝对生物利用度为42%。
两种抗蛇毒血清制剂静脉给药后的药代动力学未观察到差异。相反,肌肉注射给药后吸收速率和程度降低。