Toutain P L, Brandon R A, de Pomyers H, Alvinerie M, Baggot J D
Am J Vet Res. 1984 Sep;45(9):1750-6.
Pharmacokinetics of dexamethasone and prednisolone were studied in 6 horses given dexamethasone alcohol (IV or IM) or dexamethasone 21-isonicotinate as a solution IV or IM (50 micrograms/kg of body weight), prednisolone 21-sodium succinate IV or IM (0.6 mg/kg of body weight), or prednisolone acetate IM (0.6 mg/kg of body weight). Plasma concentrations were determined using a high-performance liquid chromatographic method. After dexamethasone alcohol (IV) or dexamethasone 21-isonicotinate (IV), the half-life of elimination was similar (53 minutes) for both formulations. After dexamethasone (alcohol and isonicotinate, IM), concentrations were low or nondetected. After prednisolone 21-sodium succinate (IV), the half-life of elimination (99.5 minutes) was significantly (P less than 0.01) longer than that for dexamethasone. After prednisolone 21-sodium succinate (IM), absorption was rapid and bioavailability was high. After prednisolone acetate (IM), absorption was slow and prednisolone was present in plasma for about 7 days. Due to the nonlinearity of prednisolone kinetics, a bioavailability higher than 100% was obtained. The basal plasma hydrocortisone concentration was approximately 70 ng/ml. After dexamethasone (IV or IM), plasma hydrocortisone values decreased after a 2-hour delay and returned to base line after a 3 to 4 day delay. After prednisolone 21-sodium succinate (IV or IM), plasma hydrocortisone decreased immediately (IV) or rapidly (IM) and returned to base line after a 24-hour delay. After prednisolone acetate (IM), plasma hydrocortisone decreased for up to 21 days.
研究了6匹马使用地塞米松醇(静脉注射或肌肉注射)、地塞米松21-异烟酸盐溶液(静脉注射或肌肉注射,50微克/千克体重)、泼尼松龙21-琥珀酸钠(静脉注射或肌肉注射,0.6毫克/千克体重)或醋酸泼尼松龙(肌肉注射,0.6毫克/千克体重)后的地塞米松和泼尼松龙的药代动力学。使用高效液相色谱法测定血浆浓度。静脉注射地塞米松醇或静脉注射地塞米松21-异烟酸盐后,两种制剂的消除半衰期相似(53分钟)。肌肉注射地塞米松(醇和异烟酸盐)后,浓度较低或未检测到。静脉注射泼尼松龙21-琥珀酸钠后,消除半衰期(99.5分钟)显著长于地塞米松(P<0.01)。肌肉注射泼尼松龙21-琥珀酸钠后,吸收迅速且生物利用度高。肌肉注射醋酸泼尼松龙后,吸收缓慢,泼尼松龙在血浆中存在约7天。由于泼尼松龙动力学的非线性,获得了高于100%的生物利用度。基础血浆氢化可的松浓度约为70纳克/毫升。静脉注射或肌肉注射地塞米松后,血浆氢化可的松值在延迟2小时后下降,并在延迟3至4天后恢复到基线。静脉注射或肌肉注射泼尼松龙21-琥珀酸钠后,血浆氢化可的松立即(静脉注射)或迅速(肌肉注射)下降,并在延迟24小时后恢复到基线。肌肉注射醋酸泼尼松龙后,血浆氢化可的松下降长达21天。