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在限制液体摄入和高液体摄入情况下单次静脉注射FCE 22101后的尿液恢复情况及耐受性

Urinary recovery and tolerability of FCE 22101 following single intravenous administration under restricted and high fluid intake.

作者信息

Sassella D, Cassinelli G, Corigli R, Dewland P, Hutt V, Lode H, Ballard R C

机构信息

Farmitalia Carlo Erba, Research and Development, Milan, Italy.

出版信息

J Antimicrob Chemother. 1989 Mar;23 Suppl C:197-203. doi: 10.1093/jac/23.suppl_c.197.

Abstract

The urinary recovery and tolerability of FCE 22101, a broad spectrum injectable penem, were investigated in a multicentre single-blind randomized crossover study of 60 healthy male volunteers. Single 1 g doses of FCE 22101 or placebo were given by intravenous bolus at weekly intervals. FCE 22101 was given either after intake of 750 ml water (treatment A) or after 8 h of water restriction (treatment B). Placebo was given under water restriction (treatment C). Urine samples obtained at timed intervals were assayed for FCE 22101 and its metabolites P1 and P2 by HPLC. The 24 h urinary recoveries of the parent drug and its metabolites were similar after treatments A and B. Mean recoveries +/- S.D were 29 +/- 13% (FCE 22101), 31 +/- 12% (P1) and 7 +/- 2% (P2) of the dose. Transient suprapubic pain or dysuria, or both, were reported by two subjects after treatment A and by six subjects after treatment B. Symptoms were associated with low urine volumes at 0-2 h and low urinary recovery of FCE 22101 and metabolite P1.

摘要

在一项针对60名健康男性志愿者的多中心单盲随机交叉研究中,对广谱注射用青霉烯类药物FCE 22101的尿液回收率和耐受性进行了研究。每周间隔静脉推注单剂量1 g的FCE 22101或安慰剂。FCE 22101在摄入750 ml水后给药(治疗A)或在限水8小时后给药(治疗B)。安慰剂在限水条件下给药(治疗C)。通过高效液相色谱法(HPLC)对定时采集的尿液样本进行FCE 22101及其代谢产物P1和P2的测定。治疗A和B后,母体药物及其代谢产物的24小时尿液回收率相似。剂量的平均回收率±标准差分别为29±13%(FCE 22101)、31±12%(P1)和7±2%(P2)。治疗A后有两名受试者报告了短暂的耻骨上疼痛或排尿困难,或两者皆有,治疗B后有六名受试者报告了上述症状。这些症状与0 - 2小时尿量少以及FCE 22101和代谢产物P1的尿液回收率低有关。

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