氯己定的两亲性及其对变形链球菌GS-5的毒性研究。

S Koontongkaew, S Jitpukdeebodintra
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引用次数: 6

摘要

通过测定二光酸氯己定的杀菌活性比较确定其对变形链球菌GS-5的毒性,并采用瑞祖脲还原法研究其对微生物脱氢酶的抑制作用。两种方法均表明,在0.75 ~ 5.00 mg/l范围内,氯己定对变形链球菌具有高毒性,可能是由于其对脱氢酶活性的抑制作用,且毒性程度与浓度密切相关。为了更好地了解氯己定的两亲性与其对变形链球菌的毒性之间的关系,研究了溶剂极性对脱氢酶抑制的影响。在反应混合物中加入5%丙酮会导致溶剂极性降低,但不会增强氯己定的毒性。这表明氯己定的抗菌作用主要是由于它的亲水性,亲脂基团的性质只是次要的。
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Amphiphilic property of chlorhexidine and its toxicity against Streptococcus mutans GS-5.

The toxicity of chlorhexidine digluconate against Streptococcus mutans GS-5 was comparatively determined by measuring its bactericidal activity, and its inhibitory effect on microbial dehydrogenases was studied by the resazurin reduction method. Both methods indicated that chlorhexidine within the range 0.75-5.00 mg/l was highly toxic to Streptococcus mutans, probably due to inhibition of dehydrogenase activity, and the extent of toxicity was closely associated with concentration. In an attempt to better understand the relationship between the amphiphilic nature of chlorhexidine and its toxicity against Streptococcus mutans, the effect of solvent polarity on dehydrogenase inhibition was investigated. A decrease in solvent polarity, induced by inclusion of 5% acetone in the reaction mixture, did not enhance the toxicity of chlorhexidine. This implies that the antimicrobial action of chlorhexidine is mainly attributable to its hydrophilicity, and that the nature of the lipophilic groups is only of secondary importance.

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