[蛋白胨和水解物对呋喃妥英硝基制剂抑菌活性的影响]。

D Marica, I Chissacof, M Corlăţean, Z Dancea, I Miclea, C Oprea
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引用次数: 0

摘要

对产物呋喃妥英(10和100 mcg)对324株革兰氏阴性菌的抑菌活性测定表明,在确定成分的培养基(7SG)上的抑菌带直径和MIC值明显大于在mumiller - hinton (MH)培养基上的抑菌带直径和MIC值,在细菌-tryptose (BT)培养基上的抑菌带直径和MIC值。增加8-12 mm phi或2-4倍二元稀释,在MH和BT介质上的解释从抗性变为敏感性。在常规培养基上记录的低结果表明蛋白胨和呋喃妥英之间存在拮抗作用,类似于已知的磺胺类药物。作者认为,蛋白胨的拮抗作用阻碍了对硝基糠醛衍生物活性的认识和对细菌敏感性的正确评价。他们还认为小剂量呋喃妥因微片(10微克)和磺胺微片(30微克)的消除趋势值得怀疑,因为它们的明显不足可能不是由于物质收缩不足,而是由于检测介质不充分。结果呼吁使用具有明确化学成分的培养基,不使用磺胺和硝基呋喃拮抗剂,并重新考虑几个方法学问题:使用具有明确化学成分的培养基;引入最大100微克/微片的中间剂量;磺胺呋喃唑和呋喃妥英敏感性分类的再评价。
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[Changes in the antibacterial activity of nitrofurantoin preparations induced by peptone and hydrolysates].

The determination of the activity of the product nitrofurantoin (10 and 100 mcg) versus 324 strains of Gram-negative bacteria showed that the diameter of the inhibition zones and the MIC values on a medium with a definite composition (7SG) are considerably larger than on the Mueller-Hinton (MH) medium, in the bacto-tryptose (BT) medium. An increase with 8-12 mm phi or with 2-4 binary dilutions changes the interpretation from resistant, on the MH and BT media into sensitive on the 7SG medium. The low results recorded on the conventional media reveal the existence of an antagonism between peptone and nitrofurantoin, similar to that known for sulfamides. The authors believe that the peptone antagonism has hindered the knowledge of the activity of the nitrofurfural derivatives and the correct assessment of the bacteria sensitivity. They also consider questionable the elimination tendency of the small dosage of microtablets of nitrofurantoin (10 mcg) and sulfamide (30 mcg), since their apparent insufficiency might be due less to the inadequate contraction of substances and more to the inadequate testing media. The results plead for the use of the media with definite chemical composition sulfamide and nitrofuran antagonists free and for reconsideration of several methodologic problems: use of the media with definite chemical composition; introduction of an intermediary dosage of maximum 100 mcg/microtablet; reassessment of the sensitivity categories for sulphafurazole and nitrofurantoin.

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