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含舒巴坦的β-内酰胺酶抑制剂复方制剂

Sulbactam-containing beta-lactamase inhibitor combinations.

作者信息

Akova M

机构信息

Department of Medicine, Section of Infectious Diseases, Hacettepe University School of Medicine, Ankara, Turkey.

出版信息

Clin Microbiol Infect. 2008 Jan;14 Suppl 1:185-8. doi: 10.1111/j.1469-0691.2007.01847.x.

Abstract

Sulbactam irreversibly inhibits the hydrolytic activity of beta-lactamases. This compound is commercially available in combination with either ampicillin or cefoperazone. In each instance, the activity of the partner antibiotic against beta-lactamase-producing bacteria is restored. One of the particular advantages of using sulbactam-containing combinations is that sulbactam itself has inherent activity against some Acinetobacter baumannii. Sulbactam combinations have not demonstrated strong selective pressures for extended-spectrum beta-lactamase-producing Enterobacteriaceae and vancomycin-resistant enterococci. In contrast to clavulanate, sulbactam does not induce class I (Ampc) chromosomal beta-lactamases in Enterobacteriaceae.

摘要

舒巴坦不可逆地抑制β-内酰胺酶的水解活性。该化合物在商业上可与氨苄西林或头孢哌酮联合使用。在每种情况下,配对抗生素对产β-内酰胺酶细菌的活性都会恢复。使用含舒巴坦组合的一个特别优点是舒巴坦本身对某些鲍曼不动杆菌具有内在活性。舒巴坦组合对产超广谱β-内酰胺酶的肠杆菌科细菌和耐万古霉素肠球菌未表现出强大的选择压力。与克拉维酸不同,舒巴坦不会在肠杆菌科细菌中诱导I类(Ampc)染色体β-内酰胺酶。

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