Dept of Biological & Agricultural Engineering, College Station, TX 77843-2117, USA.
J Food Sci. 2011 Mar;76(2):N16-24. doi: 10.1111/j.1750-3841.2010.01985.x. Epub 2011 Feb 1.
Eugenol and trans-cinnamaldehyde are natural compounds known to be highly effective antimicrobials; however, both are hydrophobic molecules, a limitation to their use within the food industry. The goal of this study was to synthesize spherical poly (DL-lactide-co-glycolide) (PLGA) nanoparticles with entrapped eugenol and trans-cinnamaldehyde for future antimicrobial delivery applications. The emulsion evaporation method was used to form the nanoparticles in the presence of poly (vinyl alcohol) (PVA) as a surfactant. The inclusion of antimicrobial compounds into the PLGA nanoparticles was accomplished in the organic phase. Synthesis was followed by ultrafiltration (performed to eliminate the excess of PVA and antimicrobial compound) and freeze-drying. The nanoparticles were characterized by their shape, size, entrapment efficiency, and antimicrobial efficiency. The entrapment efficiency for eugenol and trans-cinnamaldehyde was approximately 98% and 92%, respectively. Controlled release experiments conducted in vitro at 37 °C and 100 rpm for 72 h showed an initial burst followed by a slower rate of release of the antimicrobial entrapped inside the PLGA matrix. All loaded nanoparticles formulations proved to be efficient in inhibiting growth of Salmonella spp. (Gram-negative bacterium) and Listeria spp. (Gram-positive bacterium) with concentrations ranging from 20 to 10 mg/mL. Results suggest that the application of these antimicrobial nanoparticles in food systems may be effective at inhibiting specific pathogens.
Nanoencapsulation of lipophilic antimicrobial compounds has great potential for improving the effectiveness and efficiency of delivery in food systems. This study consisted of synthesizing PLGA nanoparticles with entrapped eugenol and trans-cinnamaldehyde. By characterizing these new delivery systems, one can understand the controlled-release mechanism and antimicrobial efficiency that provides a foundation that will enable food manufacturers to design smart food systems for future delivery applications, including packaging and processing, capable of ensuring food safety to consumers.
丁香酚和反式肉桂醛是众所周知的高效抗菌天然化合物;然而,两者都是疏水分子,这限制了它们在食品工业中的应用。本研究的目的是合成包埋丁香酚和反式肉桂醛的球形聚(DL-丙交酯-共-乙交酯)(PLGA)纳米粒子,用于未来的抗菌药物输送应用。乳液蒸发法在聚(聚乙烯醇)(PVA)作为表面活性剂的存在下形成纳米粒子。抗菌化合物被包埋在 PLGA 纳米粒子中是在有机相中完成的。合成后进行超滤(以去除过量的 PVA 和抗菌化合物)和冷冻干燥。纳米粒子的形状、大小、包封效率和抗菌效率进行了表征。丁香酚和反式肉桂醛的包封效率分别约为 98%和 92%。在 37°C 和 100 rpm 下进行的体外控释实验 72 h 表明,在 PLGA 基质中包埋的抗菌剂最初迅速释放,随后释放速度较慢。所有负载纳米粒子的配方都被证明能有效抑制沙门氏菌(革兰氏阴性菌)和李斯特菌(革兰氏阳性菌)的生长,浓度范围为 20 至 10mg/mL。结果表明,这些抗菌纳米粒子在食品系统中的应用可能有效地抑制特定的病原体。
脂溶性抗菌化合物的纳米封装具有提高食品系统中输送效果和效率的巨大潜力。本研究包括合成包埋丁香酚和反式肉桂醛的 PLGA 纳米粒子。通过对这些新的输送系统进行表征,可以了解控制释放机制和抗菌效率,为食品制造商设计未来输送应用的智能食品系统提供基础,包括包装和加工,以确保消费者的食品安全。