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比较三种与具有胶原释放系统的涤纶血管移植物结合的抗生素的抗葡萄球菌活性的疗效和持续时间。

Efficacy and duration of antistaphylococcal activity comparing three antibiotics bonded to Dacron vascular grafts with a collagen release system.

作者信息

Chervu A, Moore W S, Chvapil M, Henderson T

机构信息

Department of Surgery, University of California/Los Angeles Center for the Health Sciences 90024-6094.

出版信息

J Vasc Surg. 1991 Jun;13(6):897-901. doi: 10.1067/mva.1991.27349.

Abstract

Type 1 collagen, minimally cross-linked, was used to bind one of three antibiotics (amikacin, chloramphenicol, or rifampin) to double-velour Dacron grafts to develop a prosthesis resistant to infection. Six millimeter disks of graft were placed in separate flasks (specific for each antibiotic) containing albumin in saline and continuously agitated. At daily intervals the solution was changed, and paired graft samples were removed and placed on a blood agar plate confluently streaked with bacteria. The initial zone of inhibition (centimeters squared), the time to 50% reduction of initial inhibition zone, and the overall duration of antibacterial activity were recorded on an exponential model. Grafts bonded with amikacin and chloramphenicol had an overall duration of activity of only 2 and 1 day, respectively, against Staphylococcus aureus. The collagen bonded rifampin grafts had an initial zone of 14.76 cm,2 took 3.92 days to reach 50% of initial inhibition, and had an overall duration of activity of 22.4 days. This was significantly better than grafts preclotted with 1.0 ml of rifampin (60 mg/ml) and 9 ml of blood (10.92 cm,2 1.06 days, and 5.6 days). When tested against a slime-producing Staphylococcus epidermidis (American Type Culture Collection No. 35983), the graft bonded with rifampin had inhibitory activity of up to 27.77 days with a 50% of activity eluted at 4.78 days, significantly better than the preclotted rifampin graft without collagen bonding. These data suggest that rifampin bonded by collagen can protect a vascular graft against infection from S. aureus and S. epidermidis for up to 3 weeks after implantation.

摘要

使用轻度交联的I型胶原将三种抗生素(阿米卡星、氯霉素或利福平)之一结合到双层丝绒涤纶移植物上,以开发抗感染的假体。将6毫米的移植物圆盘放入单独的烧瓶(每种抗生素专用)中,烧瓶中含有盐水中的白蛋白,并持续搅拌。每天更换溶液,取出配对的移植物样本,并排放在涂有细菌的血琼脂平板上。在指数模型上记录初始抑菌圈(平方厘米)、初始抑菌圈减少50%的时间以及抗菌活性的总持续时间。与阿米卡星和氯霉素结合的移植物对金黄色葡萄球菌的总活性持续时间分别仅为2天和1天。胶原结合利福平的移植物初始抑菌圈为14.76平方厘米,达到初始抑菌圈50%需要3.92天,总活性持续时间为22.4天。这明显优于预先用1.0毫升利福平(60毫克/毫升)和9毫升血液预凝的移植物(10.92平方厘米、1.06天和5.6天)。当针对产黏液的表皮葡萄球菌(美国典型培养物保藏中心编号35983)进行测试时,与利福平结合的移植物具有长达27.77天的抑制活性,在4.78天洗脱50%的活性,明显优于未进行胶原结合的预先预凝利福平移植物。这些数据表明,胶原结合的利福平可在植入后长达3周的时间内保护血管移植物免受金黄色葡萄球菌和表皮葡萄球菌的感染。

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