Department of Chemistry, College of Science, King Faisal University, Al-Ahsa 31982, Saudi Arabia; Department of Chemistry, Faculty of Science, Sohag University, Sohag 82524, Egypt.
Department of Chemistry, College of Science, King Faisal University, Al-Ahsa 31982, Saudi Arabia.
Food Chem. 2024 Dec 15;461:140719. doi: 10.1016/j.foodchem.2024.140719. Epub 2024 Aug 14.
This study investigates the extract of the bioactive compounds from green coffee extract (GCE) and the loading of two different concentrations of GCE (1% and 2%) onto carrageenan nanogels (CAR NGs) to compare their antibacterial and antibiofilm effects with unloaded nanogels (NGs). The bioactive compounds of GCE were characterized using GC-MS analysis. The GCE1 and GCE2 were successfully deposited onto the surface of CAR NGs. The antibacterial and antibiofilm potential of prepared NGs were conducted against some foodborne pathogens (E. coli O157, Salmonella enterica, Staphylococcus aureus, and Listeria monocytogenes). The results of GC-MS analysis indicated that there were identified 16 bioactive compounds in GCE, including caffeine (36.27%), Dodemorph (9.04%), and D-Glycero-d-ido-heptose (2.44%), contributing to its antimicrobial properties. The antibacterial coatings demonstrated a notable antimicrobial effect, showing zone of inhibition (ZOI) diameters of up to 37 mm for GCE2 loaded CAR NGs. The minimum inhibitory concentration (MIC) values for GCE2 loaded CAR NGs were 80 ppm for E. coli O157, and 120 ppm for S. enterica, S. aureus, and L. monocytogenes, achieving complete bacterial inactivation within 10-15 min of exposure. Both GCE1 and GCE2 loaded CAR NGs significantly reduced biofilm cell densities on stainless steel (SS) materials for E. coli O157, S. enterica, S. aureus, and L. monocytogenes, with reductions ranging from 60% to 95%. Specifically, biofilm densities were reduced by up to 95% for E. coli O157, 89% for S. enterica, 85% for S. aureus, and 80% for L. monocytogenes. Results of the toxicity evaluation indicated that the NGs were non-toxic and biocompatible, with predicted EC values proved their biocompatibility and safety. These results recommended that GCE loaded CAR NGs are promising as natural antimicrobial agents for enhancing food safety and extending shelf life. Further, the study concluded that incorporating GCE into CAR NGs is an effective strategy for developing sustainable antimicrobial coatings for the food industry and manufacturing.
本研究旨在研究从绿咖啡豆提取物(GCE)中提取的生物活性化合物,并将两种不同浓度的 GCE(1%和 2%)负载到卡拉胶纳米凝胶(CAR NGs)上,以比较它们与未负载纳米凝胶(NGs)的抗菌和抗生物膜效果。使用 GC-MS 分析对 GCE 的生物活性化合物进行了表征。成功地将 GCE1 和 GCE2 沉积在 CAR NGs 的表面上。对制备的 NGs 的抗菌和抗生物膜潜力进行了测试,以评估其对一些食源性致病菌(大肠杆菌 O157、肠炎沙门氏菌、金黄色葡萄球菌和单核细胞增生李斯特菌)的抑制作用。GC-MS 分析结果表明,GCE 中鉴定出 16 种生物活性化合物,包括咖啡因(36.27%)、Dodemorph(9.04%)和 D-甘油-D-ido-庚糖(2.44%),这有助于其抗菌性能。抗菌涂层表现出显著的抗菌效果,负载 GCE2 的 CAR NGs 的抑菌环(ZOI)直径高达 37mm。负载 GCE2 的 CAR NGs 的最小抑菌浓度(MIC)值分别为 80ppm 大肠杆菌 O157 和 120ppm 肠炎沙门氏菌、金黄色葡萄球菌和单核细胞增生李斯特菌,在暴露 10-15 分钟内即可完全灭活细菌。负载 GCE1 和 GCE2 的 CAR NGs 显著降低了不锈钢(SS)材料上大肠杆菌 O157、肠炎沙门氏菌、金黄色葡萄球菌和单核细胞增生李斯特菌的生物膜细胞密度,降低幅度为 60%-95%。具体而言,大肠杆菌 O157 的生物膜密度降低了 95%,肠炎沙门氏菌降低了 89%,金黄色葡萄球菌降低了 85%,单核细胞增生李斯特菌降低了 80%。毒性评估结果表明,NGs 无毒且生物相容,预测 EC 值证明了它们的生物相容性和安全性。这些结果表明,负载 GCE 的 CAR NGs 有望作为天然抗菌剂,提高食品安全并延长保质期。此外,该研究得出结论,将 GCE 纳入 CAR NGs 是为食品工业和制造业开发可持续抗菌涂层的有效策略。