Joos Mathieu, Vackier Thijs, Mees Maarten A, Coppola Guglielmo, Alexandris Stelios, Geunes Robbe, Thielemans Wim, Steenackers Hans P L
Department of Microbial and Molecular Systems, Centre of Microbial and Plant Genetics (CMPG), KU Leuven, Leuven 3001, Belgium.
Department of Chemical Engineering, KU Leuven, Sustainable Materials Lab (SusMat), Kortrijk 8500, Belgium.
ACS Appl Bio Mater. 2024 Dec 16;7(12):8223-8235. doi: 10.1021/acsabm.4c00942. Epub 2024 Nov 26.
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 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 , , MRSA, , , , , and two strains of . 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 UTI89 and in the suspension above the hydrogel, while the staphylococci strains and are already inhibited by fully deprotonated GA (pH = 6.8). and 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在生物医学应用中备受关注。甘草酸(GA)是一种抗菌剂,由于其三个羧基的pKa值不同,GA可形成pH依赖性水凝胶。然而,GA质子化对抗菌活性的影响此前从未被研究过。因此,我们研究了pH对GA针对大肠杆菌UTI89、肺炎克雷伯菌、耐甲氧西林金黄色葡萄球菌(MRSA)、粪肠球菌、屎肠球菌、奇异变形杆菌以及两株沙门氏菌的抗菌活性的影响。一般来说,GA的抗菌活性随着pH降低(即GA质子化增加)而增强。更具体地说,对于水凝胶上方悬浮液中的大肠杆菌UTI89和肺炎克雷伯菌,需要完全质子化的GA水凝胶(pH = 3)来抑制生长和杀灭细菌,而葡萄球菌菌株和粪肠球菌在完全去质子化的GA(pH = 6.8)作用下就已被抑制。大肠杆菌DH5α和沙门氏菌表现出中等敏感性,因为它们在pH 3.8、含有部分质子化GA的水凝胶作用下被完全抑制,但在完全去质子化的GA(pH = 6.8)作用下则不会。水凝胶的抗菌活性不能仅仅归因于悬浮液pH的降低,因为GA的存在显著增强了活性。相反,这种增强的活性是由于GA从水凝胶释放到悬浮液中,并在那里直接与细菌相互作用。此外,我们通过用GA质子化分布不同的GA溶液处理病原体,提供了证据表明抗菌活性的pH依赖性是由于GA质子化状态的差异。最后,我们通过液相色谱 - 质谱联用(LC - MS)表明GA没有化学或酶促分解。总体而言,我们的结果表明pH不仅影响GA水凝胶的物理性质,还影响其抗菌性能。