广谱仿生抗菌系统

Heidi A. Wright, B. Brehm-Stecher
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引用次数: 0

摘要

抗菌肽(AMPs)是宿主免疫反应的有效成分,广泛分布于自然界。最近,模仿天然AMPs结构的无毒抗菌聚合物已经被设计出来,并正在作为新型治疗药物进行商业开发。与天然肽相比,这些化合物具有几个潜在的优势,包括更大的稳定性和更低的免疫原性,相对简单和可扩展的合成以及通过组合方法定制或“微调”其活性的能力。在之前的工作中,我们证明了某些通常被认为是安全的(GRAS)香料和香气化合物作为临床重要抗生素的吸收和活性增强剂的效用(Brehm-Stecher & Johnson, 2003)。在这里,我们已经扩展了这种方法,包括增强仿生抗菌聚合物。三种低分子量(D),广谱芳基酰胺聚合物(PolyMedix, Inc., Radnor, PA)检测了它们对革兰氏阴性菌,革兰氏阳性菌,酵母和丝状真菌的抗菌活性,无论是单独使用还是与倍半萜类增强剂共同使用。检测形式包括圆盘扩散、自动比浊法、抗菌处理细胞悬液的时间过程(动力学)电镀、1- n -苯萘胺(NPN)外膜检测和透射电子显微镜(TEM)。尽管结果因使用的聚合物和测试生物而异,但与仅使用聚合物的处理相比,含有倍半萜的处理要么增加了zoi,降低了mic,要么更快地失活。以十进制还原次数(d值)表示的抗菌活性表明,与大肠杆菌ATCC 25922孵育5 min后,倍半萜类与聚合物的结合率与对照显著差异(p < 0.05), d值为3.92 min。总的来说,我们的研究结果表明,倍半萜类增强剂与仿生抗菌聚合物的结合为开发新的、快速的、更有效的抗菌疗法提供了希望。
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Wide-spectrum biomimetic antimicrobial systems
Antimicrobial peptides (AMPs) are effective components of the host immune response and are widely distributed throughout nature. Recently, nontoxic antimicrobial polymers that mimic the structures of naturally occurring AMPs have been designed and are under development commercially as novel therapeutics. These compounds have several potential advantages over natural AMPs, including greater stability and reduced immunogenicity compared to natural peptides, relatively simple and scalable syntheses and the ability to tailor or “fine tune” their activities through combinatorial approaches. In previous work, we demonstrated the utility of certain generally regarded as safe (GRAS) flavorant and aroma compounds as enhancers of uptake and activity of clinically important antibiotics (Brehm-Stecher & Johnson, 2003). Here, we have extended this approach to include enhancement of biomimetic antimicrobial polymers. Three low molecular weight (<1000 >D), broad-spectrum arylamide polymers (PolyMedix, Inc., Radnor, PA) were examined for their antimicrobial activities against gram-negative bacteria, gram-positive bacteria, yeast and filamentous fungi, both alone and when co-administered with sesquiterpenoid enhancers. Assay formats included disk diffusion, automated turbidimetry, time course (kinetic) plating of antimicrobial-treated cell suspensions, outer membrane assays with 1-N-phenylnaphthylamine (NPN) and transmission electron microscopy (TEM). Although results differed according to the polymer and test organism used, treatments containing sesquiterpenoids were marked by either increased ZOIs, decreased MICs or more rapid inactivation when compared with polymer-only treatments. Antimicrobial activity, expressed as decimal reduction times (D-value), showed that after 5 min, the combination of sesquiterpenoid and polymer was significantly different from the controls (p < 0.05) with a D-value of 3.92 min when incubated with Escherichia coli ATCC 25922. Collectively, our results indicate that the combination of sesquiterpenoidenhancing agents with biomimetic antimicrobial polymers shows promise for the development of new, fasteracting and more broadly effective antimicrobial therapies.
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