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β-内酰胺类药物单独及与β-内酰胺酶抑制剂联合应用对具有诱导型β-内酰胺酶的铜绿假单胞菌的药效学研究。

Pharmacodynamic study of beta-lactams alone and in combination with beta-lactamase inhibitors against Pseudomonas aeruginosa possessing an inducible beta-lactamase.

作者信息

Li Chonghua, Nicolau David P, Lister Philip D, Quintiliani Richard, Nightingale Charles H

机构信息

School of Pharmacy, University of Connecticut, Storrs, CT 06269, USA.

出版信息

J Antimicrob Chemother. 2004 Feb;53(2):297-304. doi: 10.1093/jac/dkh057. Epub 2004 Jan 16.

Abstract

OBJECTIVES

The antimicrobial efficacies of beta-lactams alone and in combination with beta-lactamase inhibitors were investigated by applying a rabbit tissue cage model against a strain of Pseudomonas aeruginosa with an inducible AmpC (iAmpC) beta-lactamase.

METHODS

Two sterilized golf Wiffle balls were surgically implanted in the rabbit dorsal cervical area. After 4 weeks, Wiffle balls had filled with tissue cage fluid (TCF), in which 2 mL of 10(6) cfu/mL of the test isolate were inoculated. To achieve the same T > MIC as in humans, 400 mg/kg of the beta-lactams alone and in combination was administered twice a day via subcutaneous injection. The dosing regimens were as follows: piperacillin alone, 4 g piperacillin/0.5 g tazobactam; ticarcillin alone, 3 g ticarcillin/0.1 g clavulanate; and 3 g ticarcillin/ 0.3 g clavulanate.

RESULTS

The changes in bacterial counts (log cfu/mL) after the 3 day treatments were as follows: 1.03 +/- 0.97 (control), -1.31 +/- 0.61 (piperacillin), -2.81 +/- 0.53 (4 g piperacillin/0.5 g tazobactam), -1.61 +/- 0.68 (ticarcillin), -3.42 +/- 0.75 (3 g ticarcillin/0.1 g clavulanate) and -1.65 +/- 1.47 log cfu/mL (3 g ticarcillin/0.3 g clavulanate). AmpC induction by high-dose clavulanate was observed in rabbit TCF, and was confirmed by the in vitro induction study.

CONCLUSIONS

The study indicated that tazobactam significantly enhanced the antibacterial activity of piperacillin against iAmpC P. aeruginosa; clavulanate had synergy with the antibacterial activity of ticarcillin at low concentration, but had no effect on ticarcillin at high concentration due to AmpC induction by clavulanate.

摘要

目的

通过应用兔组织笼模型,研究β-内酰胺类药物单独使用及与β-内酰胺酶抑制剂联合使用对一株具有诱导性AmpC(iAmpC)β-内酰胺酶的铜绿假单胞菌的抗菌效果。

方法

将两个消毒后的高尔夫空心球手术植入兔颈背部区域。4周后,空心球充满组织笼液(TCF),向其中接种2 mL浓度为10(6) cfu/mL的受试分离菌。为达到与人体相同的T > MIC,单独及联合使用的β-内酰胺类药物按400 mg/kg每天皮下注射两次。给药方案如下:单独使用哌拉西林,4 g哌拉西林/0.5 g他唑巴坦;单独使用替卡西林,3 g替卡西林/0.1 g克拉维酸;以及3 g替卡西林/0.3 g克拉维酸。

结果

3天治疗后细菌计数(log cfu/mL)的变化如下:1.03 ± 0.97(对照组),-1.31 ± 0.61(哌拉西林),-2.81 ± 0.53(4 g哌拉西林/0.5 g他唑巴坦),-1.61 ± 0.68(替卡西林),-3.42 ± 0.75(3 g替卡西林/0.1 g克拉维酸)和-1.65 ± 1.47 log cfu/mL(3 g替卡西林/0.3 g克拉维酸)。在兔TCF中观察到高剂量克拉维酸诱导AmpC,体外诱导研究证实了这一点。

结论

该研究表明,他唑巴坦显著增强了哌拉西林对iAmpC铜绿假单胞菌的抗菌活性;克拉维酸在低浓度时与替卡西林的抗菌活性具有协同作用,但在高浓度时由于克拉维酸诱导AmpC而对替卡西林无作用。

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