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头孢地尼、头孢他美酯和头孢泊肟酯对淋病奈瑟菌的药敏试验解释标准及药物稳定性

Susceptibility testing interpretive criteria and drug stability for cefdinir, cefetamet, and cefpodoxime against Neisseria gonorrhoeae.

作者信息

Barrett M S, Jones R N

机构信息

Department of Pathology, University of Iowa College of Medicine, Iowa City.

出版信息

Diagn Microbiol Infect Dis. 1992 Nov-Dec;15(8):685-91. doi: 10.1016/0732-8893(92)90072-2.

Abstract

Cefdinir, cefetamet, and cefpodoxime, three orally administered cephalosporins, were tested against 100 strains of Neisseria gonorrhoeae having various antimicrobial susceptibility patterns. Triplicate testing of each organism strain was performed for all agar dilution and disk diffusion tests. Cefdinir was the most active compound (MIC90) micrograms/ml) especially against gonococci with chromosomal-mediated resistance to penicillin. The recommended susceptible interpretive criteria were as follows: for the 5-micrograms cefdinir disk, > or = 31 mm (MIC correlate, < or = 0.25 microgram/ml); for the 10-micrograms cefetament disk, > or = 29 mm (MIC correlate, < or = 0.5 microgram/ml; for the 30-micrograms cefetamet disk, > or = 31 mm (MIC correlate, < or = 0.5 microgram/ml); and for the 10-micrograms cefpodoxime disk, > or = 29 mm (MIC correlate, < or = 0.5 microgram/ml). No organisms resistant to these new cephalosporins were detected. Cefdinir, cefetamet, and defpodoxime were stable in GC agar medium for at least 21 days when stored at 2 degrees-5 degrees C.

摘要

头孢地尼、头孢他美酯和头孢泊肟酯这三种口服头孢菌素,针对100株具有不同抗菌药敏模式的淋病奈瑟菌进行了测试。对所有琼脂稀释法和纸片扩散法测试,每种菌株均进行了三次重复测试。头孢地尼是活性最强的化合物(MIC90,微克/毫升),尤其对染色体介导的青霉素耐药淋球菌。推荐的敏感判断标准如下:对于5微克头孢地尼纸片,抑菌圈直径≥31毫米(MIC对应值,≤0.25微克/毫升);对于10微克头孢他美酯纸片,抑菌圈直径≥29毫米(MIC对应值,≤0.5微克/毫升);对于30微克头孢他美酯纸片,抑菌圈直径≥31毫米(MIC对应值,≤0.5微克/毫升);对于10微克头孢泊肟酯纸片,抑菌圈直径≥29毫米(MIC对应值,≤0.5微克/毫升)。未检测到对这些新型头孢菌素耐药的菌株。头孢地尼、头孢他美酯和头孢泊肟酯在2℃-5℃储存时,在GC琼脂培养基中至少可稳定21天。

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