舒巴坦-杜鲁巴坦:针对鲍曼不动杆菌的β-内酰胺/β-内酰胺酶抑制剂组合。

IF 2.5 4区 生物学 Q3 MICROBIOLOGY Future microbiology Pub Date : 2024-01-01 Epub Date: 2024-03-01 DOI:10.2217/fmb-2023-0248
Sarah M McLeod, John P O'Donnell, Navaneeth Narayanan, John P Mills, Keith S Kaye
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引用次数: 0

摘要

舒巴坦-杜鲁巴坦是一种病原体靶向 β-内酰胺/β-内酰胺酶抑制剂复方制剂,已获得美国 FDA 批准,用于治疗 18 岁及以上患者由鲍曼不动杆菌-铜绿假单胞菌复合菌(ABC)易感性分离菌引起的医院获得性和呼吸机相关细菌性肺炎。舒巴坦是一种青霉素衍生物,对鲍曼不动杆菌具有抗菌活性,但容易被当代分离株编码的β-内酰胺酶水解。杜鲁巴坦是一种二氮杂双环辛烷 β-内酰胺酶抑制剂,对 Ambler A、C 和 D 类丝氨酸 β-内酰胺酶具有活性,可在体外和体内恢复舒巴坦对耐多药 ABC 的活性。舒巴坦-杜鲁巴坦是一种很有前途的替代疗法,可用于治疗死亡率很高的严重醋酸杆菌感染。
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Sulbactam-durlobactam: a β-lactam/β-lactamase inhibitor combination targeting Acinetobacter baumannii.

Sulbactam-durlobactam is a pathogen-targeted β-lactam/β-lactamase inhibitor combination that has been approved by the US FDA for the treatment of hospital-acquired and ventilator-associated bacterial pneumonia caused by susceptible isolates of Acinetobacter baumannii-calcoaceticus complex (ABC) in patients 18 years of age and older. Sulbactam is a penicillin derivative with antibacterial activity against Acinetobacter but is prone to hydrolysis by β-lactamases encoded by contemporary isolates. Durlobactam is a diazabicyclooctane β-lactamase inhibitor with activity against Ambler classes A, C and D serine β-lactamases that restores sulbactam activity both in vitro and in vivo against multidrug-resistant ABC. Sulbactam-durlobactam is a promising alternative therapy for the treatment of serious Acinetobacter infections, which can have high rates of mortality.

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来源期刊
Future microbiology
Future microbiology 生物-微生物学
CiteScore
4.90
自引率
3.20%
发文量
134
审稿时长
6-12 weeks
期刊介绍: Future Microbiology delivers essential information in concise, at-a-glance article formats. Key advances in the field are reported and analyzed by international experts, providing an authoritative but accessible forum for this increasingly important and vast area of research.
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