School of Physical Sciences, University of Kent, Canterbury, Kent CT2 7NH, UK.
J Mater Chem B. 2020 Jun 7;8(21):4694-4700. doi: 10.1039/d0tb00875c. Epub 2020 May 12.
SSAs are a class of supramolecular self-associating amphiphilic salt, the anionic component of which contains a covalently bound hydrogen bond donor-acceptor motif. This results in a monomeric unit which can adopt multiple hydrogen bonding modes simultaneously. Previous investigations have shown examples of SSAs to act as antimicrobial agents against clinically relevant methicillin-resistant Staphylococcus aureus (MRSA). Herein, we report an intrinsically fluorescent SSA which can self-associate producing dimers, spherical aggregates and hydrogels dependent on solvent environment, while retaining antimicrobial activity against both model Gram-positive (MRSA) and Gram-negative (Escherichia coli) bacteria. Finally, we demonstrate the SSA supramolecular hydrogel to tolerate the inclusion of the antibiotic ampicillin, leading to the enhanced inhibition of growth with both model bacteria, and derive initial molecular structure-physicochemical property-antimicrobial activity relationships.
SSA 是一类超分子自组装两亲性盐,其阴离子部分包含共价键合的氢键供体-受体基序。这导致单体单元可以同时采用多种氢键结合模式。先前的研究表明,SSA 可以作为抗微生物剂对抗临床上相关的耐甲氧西林金黄色葡萄球菌(MRSA)。在此,我们报告了一种具有内在荧光的 SSA,它可以通过自组装产生二聚体、球形聚集体和水凝胶,这取决于溶剂环境,同时保持对模型革兰氏阳性(MRSA)和革兰氏阴性(大肠杆菌)细菌的抗微生物活性。最后,我们证明 SSA 超分子水凝胶可以耐受抗生素氨苄青霉素的包含,从而增强对两种模型细菌的生长抑制作用,并得出初始分子结构-物理化学性质-抗微生物活性关系。