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妥布霉素的组织穿透性和肺部分布情况。

Tissue penetration and pulmonary disposition of tobramycin.

作者信息

Mazzei T, Novelli A, De Lalla F, Mini E, Periti P

机构信息

Dipartimento di Farmacologia, Università degli Studi di Firenze, Italy.

出版信息

J Chemother. 1995 Aug;7(4):363-70. doi: 10.1179/joc.1995.7.4.363.

Abstract

The pharmacokinetics of tobramycin, including the penetration into suction blister fluid (SBF), has been investigated in 12 patients with a mean age of 69.8 +/- 4.6 yrs, after a single i.m. administration of either 150 or 300 mg. Tobramycin demonstrated a concentration-independent pharmacokinetics and a high diffusion into the extravascular compartment with a penetration index (obtained by the SBF and serum AUC ratio) of 135% with no significant differences between the two groups of patients. Tobramycin was also administered as a single or multiple i.m. dose of 300 mg in 10 intensive care patients undergoing fiberoptic bronchoscopy for diagnostic purposes. The aminoglycoside mean concentration 6h after the single or last administration ranged from 5.3 to 5.5 mg/l and from 3.0 to 3.3 mg/l in alveolar lining fluid (ALF) and macrophages (AM), respectively, thus demonstrating that the once-daily dosage schedule leads to high and persistent levels in the bronchial alveolar tree, exceeding the minimum inhibitory concentrations in vitro for susceptible respiratory pathogens.

摘要

在12名平均年龄为69.8±4.6岁的患者中,单次肌内注射150或300mg妥布霉素后,对其药代动力学进行了研究,包括其在水疱抽吸液(SBF)中的渗透情况。妥布霉素表现出浓度依赖性药代动力学,并且向血管外间隙的扩散性较高,渗透指数(通过SBF与血清AUC比值获得)为135%,两组患者之间无显著差异。在10名因诊断目的接受纤维支气管镜检查的重症监护患者中,也给予了单次或多次300mg肌内注射剂量的妥布霉素。单次给药或末次给药后6小时,氨基糖苷类药物在肺泡衬液(ALF)和巨噬细胞(AM)中的平均浓度分别为5.3至5.5mg/L和3.0至3.3mg/L,这表明每日一次的给药方案可使支气管肺泡树中药物水平升高且持续,超过了体外对敏感呼吸道病原体的最低抑菌浓度。

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