Hobbs D C
Eur J Rheumatol Inflamm. 1983;6(1):46-55.
Piroxicam is a potent antiinflammatory agent currently in widespread use for the treatment of various inflammatory conditions of man. Following single oral doses of 10 to 100 mg, piroxicam is rapidly and fully absorbed, and eliminated with a mean plasma half life of about 45 hr. Mean peak concentrations are about 2 micrograms/ml after single 20 mg doses and about 6 micrograms/ml at steady state with 20 mg daily. Multiple peaking suggests enterohepatic recirculation of drug. In accord with expectations, steady state is achieved within 7 to 12 days with no appreciable accumulation thereafter. Due to the long plasma half life, once daily dosing provides continuous exposure to drug, with concentrations fluctuating less than twofold. Coadministration of aspirin reduces piroxicam levels by about 20 percent; antacids have no effect on piroxicam plasma concentrations.
吡罗昔康是一种强效抗炎药,目前广泛用于治疗人类的各种炎症性疾病。单次口服10至100毫克后,吡罗昔康迅速且完全吸收,平均血浆半衰期约为45小时,药物被清除。单次服用20毫克剂量后,平均峰值浓度约为2微克/毫升,每日服用20毫克达到稳态时约为6微克/毫升。多次出现峰值表明药物存在肝肠循环。不出所料,7至12天内达到稳态,此后无明显蓄积。由于血浆半衰期长,每日给药一次可使药物持续暴露,浓度波动小于两倍。阿司匹林合用可使吡罗昔康水平降低约20%;抗酸剂对吡罗昔康血浆浓度无影响。