Greenwood D, O'Grady F
J Clin Pathol. 1976 Feb;29(2):162-6. doi: 10.1136/jcp.29.2.162.
The activity of trimethoprim (TMP) and sulphamethoxazole (SMX), alone and in combination, against a sensitive strain of Escherichia coli was investigated in turbidimetric systems. In a static system in which the conditions of exposure of bacteria to drug resembled those of conventional minimum inhibitory concentration (MIC) titrations, both TMP and SMX exhibited antibacterial activity at concentrations well below the conventionally determined MIC, but regrowth occured at these concentrations during the overnight incubation period due to the emergence of adaptively resistant bacteria. Tests of combined drug action in the static turbidimetric system revealed even more synergic interaction than was apparent in conventional MIC tests. It is suggested that an important component of overall synergic interaction is the mutual suppression of adaptive "resistance" to the other agent. Studies in an in vitro model which simulates the hydrokinetic features of the urinary bladder showed that concentrations of TMP and SMX below the conventionally determined MIC inhibited the growth even of extremely dense bacterial populations so long as the concentration of drug was maintained. The response of cultures exposed to combinations of TMP and SMX in this system was so dominated by the effect of TMP that no synergic interaction with SMX was noted at concentrations of the drugs which are achievable in urine.
在比浊法系统中研究了甲氧苄啶(TMP)和磺胺甲恶唑(SMX)单独及联合使用对大肠埃希菌敏感菌株的活性。在一个静态系统中,细菌接触药物的条件类似于传统的最低抑菌浓度(MIC)滴定法,TMP和SMX在远低于传统测定的MIC浓度时均表现出抗菌活性,但在过夜培养期间,由于适应性耐药菌的出现,这些浓度下会发生细菌再生长。在静态比浊法系统中进行的联合药物作用试验显示,协同相互作用比传统MIC试验中更明显。提示总体协同相互作用的一个重要组成部分是对另一种药物适应性“耐药性”的相互抑制。在一个模拟膀胱流体动力学特征的体外模型中进行的研究表明,只要维持药物浓度,低于传统测定的MIC的TMP和SMX浓度就能抑制甚至是极高密度细菌群体的生长。在该系统中,暴露于TMP和SMX组合的培养物的反应受TMP的影响如此之大,以至于在尿液中可达到的药物浓度下,未观察到与SMX的协同相互作用。