Bergogne-Bérézin E, Muller-Serieys C, Joly-Guillou M L, Dronne N
Eur Urol. 1987;13 Suppl 1:64-8. doi: 10.1159/000472865.
A new water-soluble monobasic salt of fosfomycin with trometamol has recently been developed for oral administration. The objective of this study was to evaluate the pharmacokinetics of trometamol-fosfomycin (Monuril) in serum and in urine in 10 healthy volunteers after oral administration of one single dose (50 mg/kg). In the same volunteers the concentrations of fosfomycin were measured before and after food absorption, in serum and urine samples taken at t = 0, 2, 4, 6, 8 and 24 h after the dose (plus 0.5 and 1 h for serum samples). The measurement of fosfomycin levels was carried out by means of a microbiological procedure using Proteus mirabilis ATCC 21100 as test organism. The results indicated at 2 or 4 h serum peak levels ranging from 9 to 28 micrograms/ml, with mean values of about 17-21 micrograms/ml. The urine concentrations reached 2,000-2,500 micrograms/ml at 2 h, with high levels maintained till the 8th hour (1,200-2,750 micrograms/ml) and persistence of noticeable concentrations at 24 h (100-700 micrograms/ml). The influence of food absorption, even variable, decreased significantly the rate of absorption, with lower serum and urine levels, as measured in the same volunteers. Taking into account this factor influencing the bioavailability and the distribution of the drug, the results of the study confirm that a high proportion of the oral dose of trometamine salt of fosfomycin is absorbed; the extremely high urinary recovery of the drug even after food administration could certainly allow short-course therapy or even single-dose therapy in the treatment of uncomplicated urinary tract infection.
最近已开发出一种新的磷霉素与氨丁三醇的水溶性一元盐用于口服给药。本研究的目的是评估10名健康志愿者口服单剂量(50mg/kg)后,氨丁三醇-磷霉素(Monuril)在血清和尿液中的药代动力学。在同一志愿者中,在给药后t = 0、2、4、6、8和24小时(血清样本加0.5和1小时)采集血清和尿液样本,测量食物吸收前后的磷霉素浓度。磷霉素水平的测量采用微生物学方法,以奇异变形杆菌ATCC 21100作为测试菌株。结果表明,血清峰值水平在2或4小时时为9至28微克/毫升,平均值约为17 - 21微克/毫升。尿液浓度在2小时时达到2000 - 2500微克/毫升,高水平维持到第8小时(1200 - 2750微克/毫升),24小时时仍有明显浓度(100 - 700微克/毫升)。食物吸收的影响,即使是可变的,也显著降低了吸收速率,在同一志愿者中测量到血清和尿液水平较低。考虑到这个影响药物生物利用度和分布的因素,研究结果证实磷霉素氨丁三醇盐口服剂量的很大一部分被吸收;即使在进食后药物在尿液中的回收率极高,这肯定允许在治疗单纯性尿路感染时采用短程治疗甚至单剂量治疗。