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5-氟胞嘧啶的体外研究。

In vitro studies with 5-fluorocytosine.

作者信息

Shadomy S

出版信息

Appl Microbiol. 1969 Jun;17(6):871-7. doi: 10.1128/am.17.6.871-877.1969.

Abstract

5-Fluorocytosine, an antifungal agent with potential value as a chemotherapeutic agent, is being evaluated in the treatment of human cryptococcosis. In vitro studies with this agent have been hindered by the fact that it is inhibited significantly in the presence of partially degraded biological substances. This loss of activity is presumed to result from a competitive inhibition between the agent and its natural analogues. Procedures are described for in vitro studies with 5-fluorocytosine. These include methods for susceptibility testing and a bioassay for 5-fluorocytosine in biological fluids. Minimal inhibitory and minimal fungicidal concentrations of 5-fluorocytosine for Cryptococcus neoformans were usually in the range of 0.46 to 3.9 mug/ml and 3.9 to 15.6 mug/ml, respectively. Corresponding values for Candida albicans were 0.46 to 3.9 mug/ml and 15.6 mug/ml or greater, respectively. Strains of C. neoformans and C. albicans resistant to greater than 1,000 mug/ml were encountered both after exposure to the drug and in the absence of any known exposure. Bioassays of specimens from patients treated with 5-fluorocytosine indicated that serum and cerebrospinal fluid concentrations of 10 to 30 mug/ml and 8 to 20 mug/ml, respectively were readily achieved with a dosage of 100 mg per kg per day.

摘要

5-氟胞嘧啶是一种具有作为化疗药物潜在价值的抗真菌剂,目前正在对其治疗人类隐球菌病的效果进行评估。对该药物的体外研究受到以下事实的阻碍:在存在部分降解的生物物质时,它会受到显著抑制。这种活性丧失被认为是由于该药物与其天然类似物之间的竞争性抑制所致。本文描述了5-氟胞嘧啶的体外研究方法。这些方法包括药敏试验方法以及生物流体中5-氟胞嘧啶的生物测定法。5-氟胞嘧啶对新型隐球菌的最小抑菌浓度和最小杀菌浓度通常分别在0.46至3.9微克/毫升和3.9至15.6微克/毫升范围内。白色念珠菌的相应值分别为0.46至3.9微克/毫升和15.6微克/毫升或更高。在接触该药物后以及在没有任何已知接触的情况下,均遇到了对大于1000微克/毫升耐药的新型隐球菌和白色念珠菌菌株。对接受5-氟胞嘧啶治疗的患者的标本进行的生物测定表明,每天每千克100毫克的剂量很容易使血清和脑脊液浓度分别达到10至30微克/毫升和8至20微克/毫升。

相似文献

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In vitro studies with 5-fluorocytosine.5-氟胞嘧啶的体外研究。
Appl Microbiol. 1969 Jun;17(6):871-7. doi: 10.1128/am.17.6.871-877.1969.
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Antimicrob Agents Chemother. 1973 Jun;3(6):649-56. doi: 10.1128/AAC.3.6.649.

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