Grupo de investigación en Química y Biotecnología (QUIBIO), Facultad de Ciencias Básicas, Universidad Santiago de Cali, Calle 5 No. 62-00, Cali 760035, Colombia.
Laboratorio de Diseño y Formulación de Productos Químicos y Derivados, Departamento de Ciencias Farmacéuticas, Facultad de Ciencias Naturales, Universidad Icesi, Calle 18 No. 122-135, Cali 760035, Colombia.
Int J Mol Sci. 2019 Feb 5;20(3):680. doi: 10.3390/ijms20030680.
Bacteria are a common group of foodborne pathogens presenting public health issues with a large economic burden for the food industry. Our work focused on a solution to this problem by evaluating antibiotic activity against two bacteria ( and ) of relevance in the field of foodstuffs. We used two approaches: structural modification of the antimicrobial peptides and nano-vehiculisation of the modified peptides into polymer-coated liposomes. To achieve this, two antimicrobial peptides, herein named 'peptide +2' and 'peptide +5' were synthesised using the solid phase method. The physicochemical characterisation of the peptides was carried out using measurements of surface tension and dynamic light scattering. Additionally, nanoliposomes were elaborated by the ethanol injection method and coated with a cationic polymer (Eudragit E-100) through the layer-by-layer process. Liposome characterisation, in terms of size, polydispersity and zeta potential, was undertaken using dynamic light scattering. The results show that the degree of hydrophilic modification in the peptide leads to different characteristics of amphipathicity and subsequently to different physicochemical behaviour. On the other hand, antibacterial activity against both bacteria was slightly altered after modifying peptide sequence. Nonetheless, after the encapsulation of the peptides into polymer-coated nano-liposomes, the antibacterial activity increased approximately 2000-fold against that of .
细菌是一组常见的食源性病原体,对公众健康构成问题,并给食品工业带来巨大的经济负担。我们的工作重点是通过评估两种与食品领域相关的细菌(和)的抗生素活性来解决这个问题。我们使用了两种方法:抗菌肽的结构修饰和将修饰后的肽纳米载体化为聚合物包被的脂质体。为此,使用固相法合成了两种抗菌肽,分别命名为“肽+2”和“肽+5”。使用表面张力和动态光散射测量来进行肽的物理化学特性分析。此外,通过乙醇注入法制备纳米脂质体,并通过层层过程用阳离子聚合物(Eudragit E-100)进行涂层。使用动态光散射进行脂质体的大小、多分散性和zeta 电位的特性分析。结果表明,肽中的亲水性修饰程度导致不同的两亲性特征,从而导致不同的物理化学行为。另一方面,在修饰肽序列后,对两种细菌的抗菌活性略有改变。然而,将肽封装到聚合物包被的纳米脂质体中后,其对的抗菌活性增加了约 2000 倍。