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曲马多对局部或区域麻醉后与感染性并发症相关细菌的抗菌活性。

The antibacterial activity of tramadol against bacteria associated with infectious complications after local or regional anesthesia.

作者信息

Tamanai-Shacoori Zohreh, Shacoori Valliollah, Jolivet-Gougeon Anne, Vo Van Jean-Marie, Repère Martine, Donnio Pierre-Yves, Bonnaure-Mallet Martine

机构信息

Equipe de Microbiologie, UPRES-EA 1254, Université de Rennes I, Rennes Cedex, France.

出版信息

Anesth Analg. 2007 Aug;105(2):524-7. doi: 10.1213/01.ane.0000267525.51017.b8.

Abstract

BACKGROUND

Tramadol is a synthetic analog of codeine with opioid and local anesthetic properties. It is used as a central-acting analgesic, and recently, in subcutaneous or intradermal injections, as a local anesthetic. We investigated in vitro the antibacterial activity of tramadol in the absence of any local anesthetics against Escherichia coli, Staphylococcus aureus, Staphylococcus epidermidis, and Pseudomonas aeruginosa pathogens that can cause infectious complications after local or regional anesthesia.

METHODS

Bacterial cultures were grown for 18 h, diluted in sterile physiological saline, and incubated for 6 or 24 h at 37 degrees C with 6.25, 12.5, or 25 mg/mL tramadol. The mixtures were then plated onto blood agar and colony counts were recorded after 24 h incubation at 37 degrees C.

RESULTS

Tramadol had bactericidal activity against E. coli and S. epidermidis compared with controls: at 25 mg/mL for 6 h or at 12.5 mg/mL for 24 h, tramadol decreased by approximately 7 log(10) (P < 0.001) the colony counts of E. coli (100% kill). Similar results were obtained with S. epidermidis, with approximately 6 log(10) reduction (100% kill) when tramadol was used at 25 mg/mL for 24 h (P < 0.001). The antibacterial effect of 25 mg/mL tramadol was lower against S. aureus and P. aeruginosa, reducing the growth of these strains by approximately 3log(10) after 24 h (P < 0.001).

CONCLUSIONS

Tramadol has dose- and time-dependent bactericidal activity against E. coli and S. epidermidis, as well as antibacterial activity against S. aureus and P. aeruginosa. The antibacterial properties of tramadol may be useful for reducing the risk of bacterial infection after local or regional anesthesia.

摘要

背景

曲马多是一种具有阿片样物质和局部麻醉特性的可待因合成类似物。它被用作中枢性镇痛药,最近,在皮下或皮内注射中,用作局部麻醉药。我们在体外研究了曲马多在无任何局部麻醉药情况下对大肠杆菌、金黄色葡萄球菌、表皮葡萄球菌和铜绿假单胞菌的抗菌活性,这些病原体可在局部或区域麻醉后引起感染性并发症。

方法

细菌培养物培养18小时,用无菌生理盐水稀释,并在37℃下与6.25、12.5或25mg/mL曲马多孵育6或24小时。然后将混合物接种到血琼脂平板上,在37℃孵育24小时后记录菌落计数。

结果

与对照组相比,曲马多对大肠杆菌和表皮葡萄球菌具有杀菌活性:在25mg/mL作用6小时或12.5mg/mL作用24小时时,曲马多使大肠杆菌的菌落计数减少约7个对数(10)(P<0.001)(100%杀灭)。表皮葡萄球菌也得到了类似结果,当曲马多在25mg/mL作用24小时时,菌落计数减少约6个对数(10)(100%杀灭)(P<0.001)。25mg/mL曲马多对金黄色葡萄球菌和铜绿假单胞菌的抗菌作用较低,24小时后使这些菌株的生长减少约3个对数(10)(P<0.001)。

结论

曲马多对大肠杆菌和表皮葡萄球菌具有剂量和时间依赖性杀菌活性,对金黄色葡萄球菌和铜绿假单胞菌也具有抗菌活性。曲马多的抗菌特性可能有助于降低局部或区域麻醉后细菌感染的风险。

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