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复方磺胺甲恶唑的体内外抗菌活性。

Antibacterial activity of co-trimazine in vitro and in vivo.

作者信息

Ekström B, Fellner H, Forsgren U, Magni L, Ortengren B

出版信息

Infection. 1979;7(2):74-80. doi: 10.1007/BF01641617.

Abstract

Co-trimazine is a new drug combination especially designed for the treatment of urinary tract infections. It consists of trimethoprim (90 mg) and sulphadiazine (410 mg). When combined in vitro, the components show high activity and a high frequency of synergy against urinary tract pathogens. After oral absorption sulphadiazine has a serum half-life similar to that of trimethoprim and is excreted in active form into the urine to a much higher degree than sulphamethoxazole. The ratio of the concentrations of trimethoprim and sulphadiazine in the urine following co-trimazine is favourable for a strong synergistic action between the compounds. In cross-over studies in volunteers receiving repeated daily doses of co-trimazine, either 500 mg twice daily or 1000 mg once daily, it was found that antibacterial activity in the urine was at least as high as that provided by co-trimoxazole (2 x 960 mg) and considerably higher and more uniform than that given by nitrofurantion (3 x 50 mg).

摘要

复方磺胺嘧啶是一种专门设计用于治疗尿路感染的新型药物组合。它由甲氧苄啶(90毫克)和磺胺嘧啶(410毫克)组成。在体外联合使用时,这些成分对尿路病原体显示出高活性和高协同频率。口服吸收后,磺胺嘧啶的血清半衰期与甲氧苄啶相似,并以活性形式排泄到尿液中,其程度远高于磺胺甲恶唑。复方磺胺嘧啶给药后尿液中甲氧苄啶和磺胺嘧啶的浓度比有利于两种化合物之间产生强大的协同作用。在接受每日重复剂量复方磺胺嘧啶(每日两次500毫克或每日一次1000毫克)的志愿者的交叉研究中,发现尿液中的抗菌活性至少与复方新诺明(2×960毫克)提供的抗菌活性一样高,并且比呋喃妥因(3×50毫克)提供的抗菌活性高得多且更均匀。

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