Mathieu Joos, Thijs Vackier, Maarten A Mees, Guglielmo Coppola, Stelios Alexandris, Robbe Geunes, Wim Thielemans, Hans P L Steenackers
{"title":"Antimicrobial Activity of Glycyrrhizinic Acid Is pH-Dependent.","authors":"Mathieu Joos, Thijs Vackier, Maarten A Mees, Guglielmo Coppola, Stelios Alexandris, Robbe Geunes, Wim Thielemans, Hans P L Steenackers","doi":"10.1021/acsabm.4c00942","DOIUrl":null,"url":null,"abstract":"<p><p>In recent years, antimicrobial hydrogels have attracted much attention in biomedical applications due to their biocompatibility and high water content. Glycyrrhizin (GA) is an antimicrobial that can form pH-dependent hydrogels due to the three carboxyl groups of GA that differ in p<i>K</i><sub>a</sub> value. The influence of GA protonation on the antimicrobial activity, however, has never been studied before. Therefore, we investigated the effect of the pH on the antimicrobial activity of GA against <i>Pseudomonas aeruginosa</i>, <i>Staphylococcus aureus</i>, MRSA, <i>Staphylococcus epidermidis</i>, <i>Acinetobacter baumannii</i>, <i>Klebsiella pneumoniae</i>, <i>Klebsiella aerogenes</i>, and two strains of <i>Escherichia coli</i>. In general, the antimicrobial activity of GA increases as a function of decreasing pH (and thus increasing protonation of GA). More specifically, fully protonated GA hydrogels (pH = 3) are required for growth inhibition and killing of <i>E. coli</i> UTI89 and <i>Klebsiella</i> in the suspension above the hydrogel, while the staphylococci strains and <i>A. baumannii</i> are already inhibited by fully deprotonated GA (pH = 6.8). <i>P. aeruginosa</i> and <i>E. coli</i> DH5α showed moderate susceptibility, as they are completely inhibited by a hydrogel at pH 3.8, containing partly protonated GA, but not by fully deprotonated GA (pH = 6.8). The antimicrobial activity of the hydrogel cannot solely be attributed to the resulting pH decrease of the suspension, as the presence of GA significantly increases the activity. Instead, this increased activity is due to the release of GA from the hydrogel into the suspension, where it directly interacts with the bacteria. Moreover, we provide evidence indicating that the pH dependency of the antimicrobial activity is due to differences in GA protonation state by treating the pathogens with GA solutions differing in their GA protonation distribution. Finally, we show by LC-MS that there is no chemical or enzymatic breakdown of GA. Overall, our results demonstrate that the pH influences not only the physical but also the antimicrobial properties of the GA hydrogels.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":" ","pages":"8223-8235"},"PeriodicalIF":4.6000,"publicationDate":"2024-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1021/acsabm.4c00942","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/26 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0
Abstract
In recent years, antimicrobial hydrogels have attracted much attention in biomedical applications due to their biocompatibility and high water content. Glycyrrhizin (GA) is an antimicrobial that can form pH-dependent hydrogels due to the three carboxyl groups of GA that differ in pKa value. The influence of GA protonation on the antimicrobial activity, however, has never been studied before. Therefore, we investigated the effect of the pH on the antimicrobial activity of GA against Pseudomonas aeruginosa, Staphylococcus aureus, MRSA, Staphylococcus epidermidis, Acinetobacter baumannii, Klebsiella pneumoniae, Klebsiella aerogenes, and two strains of Escherichia coli. In general, the antimicrobial activity of GA increases as a function of decreasing pH (and thus increasing protonation of GA). More specifically, fully protonated GA hydrogels (pH = 3) are required for growth inhibition and killing of E. coli UTI89 and Klebsiella in the suspension above the hydrogel, while the staphylococci strains and A. baumannii are already inhibited by fully deprotonated GA (pH = 6.8). P. aeruginosa and E. coli DH5α showed moderate susceptibility, as they are completely inhibited by a hydrogel at pH 3.8, containing partly protonated GA, but not by fully deprotonated GA (pH = 6.8). The antimicrobial activity of the hydrogel cannot solely be attributed to the resulting pH decrease of the suspension, as the presence of GA significantly increases the activity. Instead, this increased activity is due to the release of GA from the hydrogel into the suspension, where it directly interacts with the bacteria. Moreover, we provide evidence indicating that the pH dependency of the antimicrobial activity is due to differences in GA protonation state by treating the pathogens with GA solutions differing in their GA protonation distribution. Finally, we show by LC-MS that there is no chemical or enzymatic breakdown of GA. Overall, our results demonstrate that the pH influences not only the physical but also the antimicrobial properties of the GA hydrogels.
近年来,抗菌水凝胶因其生物相容性和高含水量而在生物医学应用中备受关注。甘草苷(GA)是一种抗菌剂,由于 GA 的三个羧基的 pKa 值不同,它可以形成依赖于 pH 值的水凝胶。然而,GA 质子化对其抗菌活性的影响还从未被研究过。因此,我们研究了 pH 值对 GA 针对铜绿假单胞菌、金黄色葡萄球菌、MRSA、表皮葡萄球菌、鲍曼不动杆菌、肺炎克雷伯菌、产气克雷伯菌和两株大肠埃希菌的抗菌活性的影响。一般来说,GA 的抗菌活性会随着 pH 值的降低(从而增加 GA 的质子化)而增加。更具体地说,完全质子化的 GA 水凝胶(pH = 3)需要抑制生长并杀死水凝胶上方悬浮液中的大肠杆菌 UTI89 和克雷伯氏菌,而完全去质子化的 GA(pH = 6.8)已经可以抑制葡萄球菌菌株和鲍曼不动杆菌。铜绿假单胞菌和大肠杆菌 DH5α 显示出中等的敏感性,因为它们在 pH 值为 3.8、含有部分质子化 GA 的水凝胶中受到完全抑制,但在完全去质子化 GA(pH 值为 6.8)中则没有抑制作用。水凝胶的抗菌活性不能完全归因于悬浮液 pH 值的降低,因为 GA 的存在会显著提高抗菌活性。相反,这种活性的提高是由于 GA 从水凝胶中释放到悬浮液中,在悬浮液中直接与细菌发生作用。此外,我们还提供了证据,表明抗菌活性的 pH 值依赖性是由于 GA 质子状态的差异造成的,方法是用 GA 质子分布不同的 GA 溶液处理病原体。最后,我们通过液相色谱-质谱联用仪(LC-MS)表明,GA 没有被化学或酶分解。总之,我们的研究结果表明,pH 值不仅会影响 GA 水凝胶的物理特性,还会影响其抗菌特性。
期刊介绍:
ACS Applied Bio Materials is an interdisciplinary journal publishing original research covering all aspects of biomaterials and biointerfaces including and beyond the traditional biosensing, biomedical and therapeutic applications.
The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrates knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important bio applications. The journal is specifically interested in work that addresses the relationship between structure and function and assesses the stability and degradation of materials under relevant environmental and biological conditions.