STUDIES OF THE ORAL BIOAVAILABILITY OF ALENDRONATE

被引:205
作者
GERTZ, BJ
HOLLAND, SH
KLINE, WF
MATUSZEWSKI, BK
FREEMAN, A
QUAN, H
LASSETER, KC
MUCKLOW, JC
PORRAS, AG
机构
[1] MERCK RES LABS,W POINT,PA
[2] CLIN PHARMACOL ASSOCIATES,MIAMI,FL
[3] INDAGO CLIN RES UNIT,STOKE ON TRENT,STAFFS,ENGLAND
关键词
D O I
10.1016/0009-9236(95)90245-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Clinical studies were performed to examine the oral bioavailability of alendronate (4-amino-1-hydroxybutylidene-1,1-bisphosphonate monosodium). All studies, with the exception of one performed in men, involved postmenopausal women. Short-term (24 to 36 hours) urinary recovery of alendronate after an intravenous dose of 125 to 250 mu g averaged about 40% in both men and women. In women, oral bioavailability of alendronate was independent of dose (5 to 80 mg) and averaged (90% confidence interval) 0.76% (0.58, 0.98) when taken with water in the fasting state, followed by a meal 2 hours later. Bioavailability was similar in men [0.59%, (0.43, 0.81)]. Taking alendronate either 60 or 30 minutes before a standardized breakfast reduced bioavailability by 40% relative to the 2-hour wait. Taking alendronate either concurrently with or 2 hours after breakfast drastically (>85%) impaired availability. Black coffee or orange juice alone, when taken with the drug, also reduced bioavailability (approximately 60%), Increasing gastric pH, by infusion of ranitidine, was associated with a doubling of alendronate bioavailability. A practical dosing recommendation, derived from these findings and reflective of the long-term nature of therapy for a disease such as osteoporosis, is that patients take the drug with water after an overnight fast and at least 30 minutes before any other food or beverage.
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页码:288 / 298
页数:11
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