Department of Pharmacy, School of Health Sciences, College of Medicine and Health Sciences, Bahir Dar University, Bahir Dar, Ethiopia.
Department of Pharmaceutics and Social Pharmacy, School of Pharmacy, College of Medicine and Health Sciences, Addis Ababa University, Addis Ababa, Ethiopia.
Int J Nanomedicine. 2023 Sep 15;18:5289-5307. doi: 10.2147/IJN.S418588. eCollection 2023.
Macrolide drugs are among the broad-spectrum antibiotics that are considered as "miracle drugs" against infectious diseases that lead to higher morbidity and mortality rates. Nevertheless, their effectiveness is currently at risk owing to the presence of devastating, antimicrobial-resistant microbes. In view of this challenge, nanotechnology-driven innovations are currently being anticipated for promising approaches to overcome antimicrobial resistance. Nowadays, various nanostructures are being developed for the delivery of antimicrobials to counter drug-resistant microbial strains through different mechanisms. Metallic nanoparticle-based delivery of macrolides, particularly using silver and gold nanoparticles (AgNPs & AuNPs), demonstrated a promising outcome with worthy stability, oxidation resistance, and biocompatibility. Similarly, macrolide-conjugated magnetic NPs resulted in an augmented antimicrobial activity and reduced bacterial cell viability against resistant microbes. Liposomal delivery of macrolides also showed favorable synergistic antimicrobial activities in vitro against resistant strains. Loading macrolide drugs into various polymeric nanomaterials resulted in an enhanced zone of inhibition. Intercalated nanomaterials also conveyed an outstanding macrolide delivery characteristic with efficient targeting and controlled drug release against infectious microbes. This review abridges several nano-based delivery approaches for macrolide drugs along with their recent achievements, challenges, and future perspectives.
大环内酯类药物是广谱抗生素之一,被认为是对抗传染性疾病的“神奇药物”,这些疾病会导致更高的发病率和死亡率。然而,由于破坏性的、抗微生物的微生物的存在,它们的有效性目前正面临风险。鉴于这一挑战,目前正在期待纳米技术驱动的创新,以寻找有前途的方法来克服抗微生物药物耐药性。如今,正在开发各种纳米结构,通过不同的机制将抗生素递送到对抗耐药微生物菌株的药物中。基于金属纳米颗粒的大环内酯类药物的递送,特别是使用银和金纳米颗粒(AgNPs 和 AuNPs),表现出了有希望的结果,具有值得关注的稳定性、抗氧化性和生物相容性。同样,大环内酯类药物偶联的磁性纳米颗粒导致对耐药微生物的抗菌活性增强和细胞活力降低。大环内酯类药物的脂质体递药也显示出体外对耐药菌株有利的协同抗菌活性。将大环内酯类药物加载到大环内酯类药物到各种聚合物纳米材料中,导致抑制区增强。夹层纳米材料也具有出色的大环内酯类药物传递特性,能够针对感染性微生物进行高效靶向和控制药物释放。本综述概述了几种基于纳米的大环内酯类药物的递药方法及其最新进展、挑战和未来展望。