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健康受试者中单环β-内酰胺类氨曲南(SQ 26,776)的单剂量药代动力学。

Single-dose pharmacokinetics of the monobactam azthreonam (SQ 26,776) in healthy subjects.

作者信息

Swabb E A, Sugerman A A, Platt T B, Pilkiewicz F G, Frantz M

出版信息

Antimicrob Agents Chemother. 1982 Jun;21(6):944-9. doi: 10.1128/AAC.21.6.944.

Abstract

Azthreonam (SQ 26,776) is a new, completely synthetic, monocyclic beta-lactam antimicrobial agent that is highly active in vitro against most gram-negative bacteria. The pharmacokinetics of single intravenous doses of 125 to 4,000 mg, studied in 36 healthy male subjects, were best described by an open, linear, two-compartment kinetic model. The mean peak serum levels at 5 min after completion of 3-min infusions of 500-, 1,000- and 2,000-mg doses were 58, 125, and 242 micrograms/ml, respectively. The mean terminal serum half-life for all doses was 1.66 h, and the apparent volume of distribution was 0.18 liter/kg. The mean serum clearance was 1.27 ml min-1 kg-1, and urinary excretion averaged 68% of the doses administered. The pharmacokinetics of single intramuscular doses of 250 to 1,000 mg, studied in 18 subjects, were best described by a linear, one-compartment model, with first-order absorption and elimination. The mean peak serum levels occurring at 1 h after doses of 250, 500, and 1,000 mg were 12, 22, and 46 micrograms/ml, respectively. Other kinetic parameters were similar to those for intravenous administration. Tolerance of azthreonam was good, with only a mild rash in one subject and with mild to moderate transient elevations in serum transaminases and lactate dehydrogenase in two subjects.

摘要

氨曲南(SQ 26,776)是一种全新的、完全合成的单环β-内酰胺类抗菌剂,在体外对大多数革兰氏阴性菌具有高度活性。在36名健康男性受试者中研究了125至4000毫克单次静脉给药的药代动力学,其最佳描述为开放、线性、二室动力学模型。在输注500毫克、1000毫克和2000毫克剂量3分钟结束后5分钟时的平均血清峰值水平分别为58、125和242微克/毫升。所有剂量的平均终末血清半衰期为1.66小时,表观分布容积为0.18升/千克。平均血清清除率为1.27毫升·分钟-1·千克-1,尿排泄量平均为给药剂量的68%。在18名受试者中研究了250至1000毫克单次肌内给药的药代动力学,其最佳描述为具有一级吸收和消除的线性一室模型。在给予250毫克、500毫克和1000毫克剂量后1小时出现的平均血清峰值水平分别为12、22和46微克/毫升。其他动力学参数与静脉给药相似。氨曲南的耐受性良好,仅1名受试者出现轻度皮疹,2名受试者出现血清转氨酶和乳酸脱氢酶轻度至中度短暂升高。

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本文引用的文献

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Parenteral toxicological profile of the monocyclic beta-lactam antibiotic SQ 26,776 in mice, rats and dogs.
J Antimicrob Chemother. 1981 Dec;8 Suppl E:141-6. doi: 10.1093/jac/8.suppl_e.141.
2
Pharmacokinetics of the monobactam SQ 26,776 after single intravenous doses in healthy subjects.
J Antimicrob Chemother. 1981 Dec;8 Suppl E:131-40. doi: 10.1093/jac/8.suppl_e.131.
5
In-vivo properties of SQ 26,776.SQ 26,776的体内特性。
J Antimicrob Chemother. 1981 Dec;8 Suppl E:123-30. doi: 10.1093/jac/8.suppl_e.123.
6
Antibacterial activity of a monocyclic beta-lactam SQ 26,776.单环β-内酰胺SQ 26,776的抗菌活性
J Antimicrob Chemother. 1981 Dec;8 Suppl E:111-22. doi: 10.1093/jac/8.suppl_e.111.

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