Toutain P L, Koritz G D, Alvinerie M, de Pomyers H, Ruckebusch Y
Am J Vet Res. 1985 Mar;46(3):719-25.
The pharmacokinetics of prednisolone were studied in a group of 6 cows given prednisolone 21-sodium succinate IV and IM (600 micrograms/kg of body weight expressed as prednisolone alcohol) and prednisolone acetate IM (600 micrograms/kg of body weight expressed as prednisolone alcohol). After IV administration of prednisolone 21-sodium succinate, the half-life of elimination was 3.6 +/- 1.177 hours. After IM administration of prednisolone 21-sodium succinate, absorption was rapid and complete. After IM administration of prednisolone acetate, absorption was very slow with an absorption half-life of 48 hours, but was still complete. Basal plasma hydrocortisone was about 7.5 ng/ml. After IV and IM administration of prednisolone 21-sodium succinate, plasma hydrocortisone returned to normal values within 48 hours. In contrast, after IM administration of prednisolone acetate, a long adrenal suppression lasting from 4 to 6 weeks was observed.
对一组6头奶牛进行了泼尼松龙的药代动力学研究,静脉注射和肌肉注射泼尼松龙21 - 琥珀酸钠(以泼尼松龙醇计600微克/千克体重)以及肌肉注射醋酸泼尼松龙(以泼尼松龙醇计600微克/千克体重)。静脉注射泼尼松龙21 - 琥珀酸钠后,消除半衰期为3.6±1.177小时。肌肉注射泼尼松龙21 - 琥珀酸钠后,吸收迅速且完全。肌肉注射醋酸泼尼松龙后,吸收非常缓慢,吸收半衰期为48小时,但仍完全吸收。基础血浆氢化可的松约为7.5纳克/毫升。静脉注射和肌肉注射泼尼松龙21 - 琥珀酸钠后,血浆氢化可的松在48小时内恢复到正常值。相比之下,肌肉注射醋酸泼尼松龙后,观察到长达4至6周的长期肾上腺抑制。