Macêdo Hanne Lazla Rafael de Queiroz, de Oliveira Lara Limeira, de Oliveira David Nattan, Lima Karitas Farias Alves, Cavalcanti Isabella Macário Ferro, Campos Luís André de Almeida
Keizo Asami Institute (iLIKA), Federal University of Pernambuco (UFPE), Recife 50670-901, PE, Brazil.
Academic Center of Vitória (CAV), Federal University of Pernambuco (UFPE), Vitória de Santo Antão 50670-901, PE, Brazil.
Antibiotics (Basel). 2024 Sep 5;13(9):844. doi: 10.3390/antibiotics13090844.
Flavonoids are secondary metabolites that exhibit remarkable biological activities, including antimicrobial properties against , a pathogen responsible for several serious nosocomial infections. However, oral administration of these compounds faces considerable challenges, such as low bioavailability and chemical instability. Thus, the encapsulation of flavonoids in nanosystems emerges as a promising strategy to mitigate these limitations, offering protection against degradation; greater solubility; and, in some cases, controlled and targeted release. Different types of nanocarriers, such as polymeric nanoparticles, liposomes, and polymeric micelles, among others, have shown potential to increase the antimicrobial efficacy of flavonoids by reducing the therapeutic dose required and minimizing side effects. In addition, advances in nanotechnology enable co-encapsulation with other therapeutic agents and the development of systems responsive to more specific stimuli, optimizing treatment. In this context, the present article provides an updated review of the literature on flavonoids and the main nanocarriers used for delivering flavonoids with antibacterial properties against
黄酮类化合物是具有显著生物活性的次生代谢产物,包括对 (一种导致多种严重医院感染的病原体)的抗菌特性。然而,口服这些化合物面临着相当大的挑战,如生物利用度低和化学不稳定性。因此,将黄酮类化合物封装在纳米系统中成为减轻这些限制的一种有前景的策略,可提供抗降解保护、更高的溶解度,并且在某些情况下实现可控和靶向释放。不同类型的纳米载体,如聚合物纳米颗粒、脂质体和聚合物胶束等,已显示出通过降低所需治疗剂量和最小化副作用来提高黄酮类化合物抗菌功效的潜力。此外,纳米技术的进步使得能够与其他治疗剂共同封装,并开发对更特定刺激有响应的系统,从而优化治疗。在此背景下,本文提供了关于黄酮类化合物以及用于递送具有抗 抗菌特性的黄酮类化合物的主要纳米载体的文献综述更新。