Department of Laboratory Medicine, Karolinska University Hospital, Karolinska Institutet, SE-14186 Stockholm, Sweden.
Int J Antimicrob Agents. 2010 Dec;36(6):537-41. doi: 10.1016/j.ijantimicag.2010.07.021.
Ceftobiprole is a new broad-spectrum pyrrolidinone cephem active against meticillin-resistant Staphylococcus aureus, vancomycin-resistant Enterococcus faecalis and Gram-negative bacteria such as Enterobacteriaceae and Pseudomonas spp. The purpose of the present study was to investigate the effect of administration of ceftobiprole on the normal intestinal microflora. Twelve healthy subjects (six males and six females) aged 20-31 years received ceftobiprole 500 mg by intravenous infusion every 8h for 7 days. Plasma samples were collected on Days -1, 1, 4, 7, 10, 14 and 21 for determination of drug concentration by biological and chemical methods. Faecal samples were collected on Days -1, 2, 4, 7, 10, 14 and 21. For analysis of the microflora, faecal specimens were cultured on non-selective and selective media. Different colony types were counted, isolated in pure culture and identified to genus level. All new colonising aerobic and anaerobic bacteria were tested for susceptibility to ceftobiprole. Plasma concentrations of ceftobiprole 10 min after completion of infusion were as follows: Day 1, 14.7-23.6 mg/L; Day 4, 15.9-24.5 mg/L; and Day 7, 15.9-23.9 mg/L. No ceftobiprole was detected in plasma on Days -1, 10, 14 and 21. No measurable concentrations of ceftobiprole were found in faeces on Days -1, 2, 4, 7, 10, 14 and 21. There were minor changes in the numbers of enteric bacteria, enterococci and Candida albicans and there were moderate changes in the numbers of bifidobacteria, lactobacilli, clostridia and Bacteroides spp. during the same period. No Clostridium difficile strains or toxins were found. No new colonising aerobic and anaerobic bacteria with ceftobiprole minimum inhibitory concentrations of ≥ 4 mg/L were found. Ceftobiprole had no significant ecological impact on the human intestinal microflora.
头孢洛林是一种新型广谱吡咯烷酮头孢菌素,对耐甲氧西林金黄色葡萄球菌、万古霉素耐药粪肠球菌和革兰氏阴性菌如肠杆菌科和假单胞菌属具有活性。本研究旨在研究头孢洛林给药对正常肠道菌群的影响。12 名健康受试者(6 名男性和 6 名女性)年龄 20-31 岁,每 8 小时静脉输注头孢洛林 500mg,共 7 天。通过生物化学方法测定血浆样本在第-1、1、4、7、10、14 和 21 天的药物浓度。在第-1、2、4、7、10、14 和 21 天采集粪便样本。为了分析微生物群,粪便标本在非选择性和选择性培养基上培养。计数不同的菌落类型,在纯培养物中分离并鉴定到属水平。所有新定植的需氧和厌氧菌均测试对头孢洛林的敏感性。输注完成后 10 分钟,头孢洛林的血浆浓度如下:第 1 天,14.7-23.6mg/L;第 4 天,15.9-24.5mg/L;第 7 天,15.9-23.9mg/L。在第-1、10、14 和 21 天,血浆中未检测到头孢洛林。在第-1、2、4、7、10、14 和 21 天,粪便中未检测到可测量浓度的头孢洛林。在此期间,肠道细菌、肠球菌和白色念珠菌的数量略有变化,双歧杆菌、乳酸杆菌、梭菌和拟杆菌属的数量中度变化。未发现艰难梭菌菌株或毒素。未发现新定植的需氧和厌氧菌,其头孢洛林最低抑菌浓度≥4mg/L。头孢洛林对人类肠道微生物群没有显著的生态影响。