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Bacterial biofilms play a significant role in increasing antibiotic resistance and the pathogenesis of Escherichia coli; their control is a major challenge in treating bacterial infections. In recent years, natural compounds have emerged as effective alternatives for inhibiting the formation and destruction of bacterial biofilms. Natural compounds such as curcumin, cinnamaldehyde, eugenol, carvacrol, quercetin, resveratrol, thymol, citral, and catechin are noteworthy in hindering and destroying E. coli biofilms. They inhibit bacterial motility (swarming and swimming), reducing attachment to surfaces, and downregulate genes related to attachment and motility (fimH, csgABC, sfaAS, papG, fliAC, flhCD, and motAB). Natural compounds can also disrupt the bacterial communication system and cause changes in the expression of luxS, sdiA, tnaA, qseBC, bssS, and lsrR genes. Studies have also shown that natural compounds can destroy mature biofilms' structure and decrease biofilm exopolysaccharides' production. This impact makes the bacteria more sensitive to the antimicrobial agents. However, one of the biggest challenges in using natural compounds is their low stability and restricted bioavailability in biological environments. For this reason, utilizing nanoparticles and novel drug delivery systems can improve these compounds' stability, penetrability, and efficacy. This article reviews the antibiofilm potential of natural compounds, their mechanisms of activity in hindering and destroying E. coli biofilms, and the role of nanotechnology in improving the performance of these compounds.
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http://dx.doi.org/10.1007/s00203-025-04434-9 | DOI Listing |
Chem Biodivers
September 2025
Instituto De Química, Universidade Federal de Mato Grosso Do Sul, Campo Grande, Brazil.
Mezilaurus duckei, a Brazilian endemic tree species found exclusively in the Amazon Rainforest, is primarily exploited for timber in construction. Due to its endangered status, this study aimed to investigate the chemical profile and biological properties of the ethanolic extract and its phases derived from M. duckei leaves.
View Article and Find Full Text PDFJ Agric Food Chem
September 2025
Department of Food Science and Engineering, Ningbo University, Ningbo 315211, P.R. China.
Sleep deprivation (SD) is a major contributor to cognitive impairment, often accompanied by central neuroinflammation and gut microbiota dysbiosis. The tryptophan (TRP) pathway, activated via indoleamine 2,3-dioxygenase (IDO), serves as a critical link between immune activation and neuronal damage. Umbelliferone (UMB), a naturally occurring coumarin compound, possesses anti-inflammatory, antioxidant, and microbiota-modulating properties.
View Article and Find Full Text PDFChem Biodivers
September 2025
Zhejiang Provincial Engineering Research Center of New Technologies and Applications for Targeted Therapy of Major Diseases, Laboratory of Anti-Allergy Functional Compounds, College of Life Sciences and Medicine, Zhejiang Sci-Tech University, Hangzhou, China.
Autoimmune diseases (AIDs), defined by irregularities in immune system function, pose a substantial health challenge worldwide, impacting millions with persistent and frequently debilitating conditions. Conventional treatments, such as glucocorticoid-based immunosuppressive therapies, are associated with notable drawbacks and limitations. In response to these difficulties, recent scientific efforts have increasingly focused on natural compounds as potential therapeutic agents.
View Article and Find Full Text PDFChem Biodivers
September 2025
Chongqing Key Laboratory of Development and Utilization of DaoDi Medicinal Materials in Three Gorges Reservoir Area, Chongqing Three Gorges Medical College, Chongqing, P. R. China.
Three new steroidal saponins, kingianoside L-N (1-3), whose structures were elucidated through comprehensive spectroscopic analysis, and 15 known compounds (4-18) were isolated from Polygonatum kingianum var. grandifolium, a source of the traditional antihyperglycemic medicine Polygonati rhizome. The effects of compounds 1-13 on α-glucosidase activity were evaluated in vitro.
View Article and Find Full Text PDFChem Biodivers
September 2025
Department of Biotechnology, Yeungnam University, Gyeongsan, Gyeongbuk, Republic of Korea.
One of the most significant problems facing the scientific community in the 21st century is diabetes mellitus. There is an urgent need to create new powerful compounds that can fight this terrible disease because the number of instances of diabetes and drug-resistant diabetes is rising. We have synthesized a novel series of thiazole-derived thiadiazole-based Schiff base derivatives (1-10) in an effort to identify potential antidiabetic agents.
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