颗粒
生物利用度
硬脂酸盐
化学
红霉素
剂型
色谱法
弹丸
药理学
材料科学
医学
生物化学
有机化学
抗生素
复合材料
作者
T. B. Tjandramaga,Anne Van Hecken,A. Mullie,René Verbesselt,P.J. De Schepper,L. Verbist,Kenneth Josefsson
出处
期刊:Pharmacology
[Karger Publishers]
日期:1984-01-01
卷期号:29 (6): 305-311
被引量:9
摘要
In a randomized three-phase crossover study, 12 healthy male volunteers were given three 12-hourly 500-mg doses of erythromycin base, as enteric coated pellets in capsules (2 × 250 mg), erythromycin stearate tablet (1 × 500 mg), or erythromycin ethylsuccinate sachet (1 × 500 mg). The reaction time after administration of the pellets is significantly longer than after the stearate or ethylsuccinate formulations. The peak serum concentrations are higher for the pellets after both the 1st and 3rd dose. The time to reach peak concentrations is significantly longer for the pellets than for the stearate and ethylsuccinate formulations. The area under the serum concentration/time curve during 0–8 h after both doses is highest for the pellets. In conclusion, these findings indicate that despite the longer lag (1.8–1.2 h), the extent of gastrointestinal absorption and bioavailability of erythromycin is apparently greater for the base pellets than for the stearate and ethylsuccinate formulations.
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