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四种给药方式对氨曲南、头孢呋辛和氨苄西林渗透至组织间液和纤维蛋白凝块的影响以及对流感嗜血杆菌的体内疗效。

Influence of four modes of administration on penetration of aztreonam, cefuroxime, and ampicillin into interstitial fluid and fibrin clots and on in vivo efficacy against Haemophilus influenzae.

作者信息

Lavoie G Y, Bergeron M G

出版信息

Antimicrob Agents Chemother. 1985 Sep;28(3):404-12. doi: 10.1128/AAC.28.3.404.

Abstract

The extravascular penetration and bactericidal activity of aztreonam, cefuroxime, and ampicillin against beta-lactamase-positive and -negative Haemophilus influenzae strains were compared in a rabbit model. All groups of animals received an identical total dose of 100 mg of either antibiotic per kg given by four different intravenous modes of administration including a single large injection, four intermittent injections, a continuous infusion, and an injection followed by an infusion. Aztreonam had a higher degree of penetration in interstitial fluid and fibrin clots and was the most effective agent against beta-lactamase-positive and -negative H. influenzae. A single large injection of either drug resulted in significantly higher peak levels and higher initial area under the curves of concentrations of drugs in serum, the interstitial fluid, and fibrin clots than those by other modes of administration. Continuous infusions of antibiotics resulted in poor in vivo bactericidal activity. Other modes of administration exhibited good antibacterial activity within the first 6 h of the study. Thereafter, a single large injection of aztreonam resulted in a much more rapid killing of H. influenzae than that by injection of the other drugs. Aztreonam and cefuroxime showed good in vivo stability to beta-lactamase produced by H. influenzae while ampicillin was rapidly hydrolyzed in vivo.

摘要

在兔模型中比较了氨曲南、头孢呋辛和氨苄西林对β-内酰胺酶阳性和阴性流感嗜血杆菌菌株的血管外渗透及杀菌活性。所有动物组均接受相同的总剂量,即每千克100毫克的上述任一抗生素,通过四种不同的静脉给药方式给予,包括单次大剂量注射、四次间歇注射、持续输注以及注射后继以输注。氨曲南在组织间液和纤维蛋白凝块中的渗透程度更高,并且是针对β-内酰胺酶阳性和阴性流感嗜血杆菌最有效的药物。单次大剂量注射任一药物所产生的血清、组织间液和纤维蛋白凝块中药物浓度的峰值水平及曲线下初始面积均显著高于其他给药方式。抗生素持续输注导致体内杀菌活性较差。在研究的最初6小时内,其他给药方式表现出良好的抗菌活性。此后,单次大剂量注射氨曲南导致杀灭流感嗜血杆菌的速度比注射其他药物要快得多。氨曲南和头孢呋辛对流感嗜血杆菌产生的β-内酰胺酶显示出良好的体内稳定性,而氨苄西林在体内迅速被水解。

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