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头孢地嗪(HR - 221)与β-内酰胺酶抑制剂联合的体外活性

In vitro activity of cefodizime (HR-221) in combination with beta-lactamase inhibitors.

作者信息

Segatore B, Perilli M, Franceschini N, Setacci D, Oratore A, Amicosante G

机构信息

Dipartimento di Scienze e Tecnologie Biomediche e di Biometria, Università dell'Aquila, Italy.

出版信息

J Chemother. 1993 Jun;5(3):147-50. doi: 10.1080/1120009x.1993.11739223.

Abstract

Cefodizime (formerly HR221) was tested either for in vitro microbiological activity or for its stability to beta-lactamases in the presence of two beta-lactamase inhibitors (clavulanic acid, tazobactam). Cefodizime was a poor substrate of class C enzymes but hyperproducer strains were generally resistant with or without a beta-lactamase inhibitor used in combination. On the contrary, class A enzymes were able to hydrolyze cefodizime. However, strains expressing class A beta-lactamase were susceptible to cefodizime in combination with clavulanic acid.

摘要

头孢地嗪(原名HR221)在两种β-内酰胺酶抑制剂(克拉维酸、他唑巴坦)存在的情况下,进行了体外微生物活性或对β-内酰胺酶稳定性的测试。头孢地嗪是C类酶的不良底物,但高产菌株无论是否联合使用β-内酰胺酶抑制剂通常都具有抗性。相反,A类酶能够水解头孢地嗪。然而,表达A类β-内酰胺酶的菌株对与克拉维酸联合使用的头孢地嗪敏感。

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