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载姜黄素和精油脂质体的抗菌和细胞毒性活性评估。

Assessment of Antimicrobial and Cytotoxic Activities of Liposomes Loaded with Curcumin and Essential Oil.

机构信息

Molecular Immunology Group (GYMOL), Center of Biomedical Research, Faculty of Health Sciences, Quindío University, Armenia 630003, Colombia.

Group of Investigation in Oral Health, Faculty of Dentistry, Antonio Nariño University, Armenia 630001, Colombia.

出版信息

Biomolecules. 2024 Jul 15;14(7):851. doi: 10.3390/biom14070851.

Abstract

(1) Introduction: Curcumin and essential oils have a broad spectrum of biological activities; however, their physicochemical instability, low solubility, and high volatility limit their therapeutic use. Encapsulation in liposomes has been reported as a feasible approach to increase the physicochemical stability of active substances, protect them from interactions with the environment, modulate their release, reduce their volatility, improve their bioactivity, and reduce their toxicity. To date, there are no reports on the co-encapsulation of curcumin and essential oils in liposomes. Therefore, the objective of this work is to prepare and physiochemical characterize liposomes loaded with the mixture of these compounds and to evaluate different in vitro biological activities. (2) Methods: Liposomes were produced using the thin-layer method and physiochemical characteristics were calculated. The antimicrobial and cytotoxic activities of both encapsulated and non-encapsulated compounds were evaluated. (3) Results: Empty and loaded nanometric-sized liposomes were obtained that are monodisperse and have a negative zeta potential. They inhibited the growth of and did not exhibit cytotoxic activity against mammalian cells. (4) Conclusions: Encapsulation in liposomes was demonstrated to be a promising strategy for natural compounds possessing antimicrobial activity.

摘要

(1) 引言:姜黄素和精油具有广泛的生物活性;然而,它们的物理化学不稳定性、低溶解度和高挥发性限制了它们的治疗用途。将其包封在脂质体中已被报道为一种可行的方法,可以提高活性物质的物理化学稳定性,保护它们免受与环境的相互作用,调节它们的释放,降低它们的挥发性,提高它们的生物活性,并降低它们的毒性。迄今为止,尚无关于姜黄素和精油在脂质体中共同包封的报道。因此,本工作的目的是制备并物理化学表征负载这些化合物混合物的脂质体,并评估不同的体外生物活性。(2) 方法:采用薄膜法制备脂质体,并计算其物理化学特性。评估了包封和未包封化合物的抗菌和细胞毒性活性。(3) 结果:得到了纳米尺寸的、单分散的、带负电荷的空脂质体和负载脂质体。它们抑制了 的生长,对哺乳动物细胞没有细胞毒性活性。(4) 结论:将具有抗菌活性的天然化合物包封在脂质体中被证明是一种很有前途的策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c5c/11275147/7d34ed251a3b/biomolecules-14-00851-g001.jpg

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