Development of solid lipid nanoparticles-loaded drugs in parasitic diseases.

0 MATERIALS SCIENCE, MULTIDISCIPLINARY Discover nano Pub Date : 2024-01-04 DOI:10.1186/s11671-023-03955-w
Sara Nemati, Mahsa Mottaghi, Parisa Karami, Hamed Mirjalali
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Abstract

Parasites cause illnesses with broad spectrum of symptoms from mild to severe, and are responsible for a significant number of outbreaks in the world. Current anti-parasitic drugs are toxic and have significant side effects. Nano-carriers are believed to obviate the limitations of conventional drugs via decreasing side effects and increasing target delivery and drug permeability with a controlled prolonged release of a drug. Solid lipid nanoparticles (SLNs) are lipid nanoparticles (LNPs), which have frequently been practiced. Suitable release rate, stability, and target delivery make SLNs a good alternative for colloidal carriers. SLNs are supposed to have great potential to deliver natural products with anti-parasitic properties. Nanoparticles have employed to improve stability and capacity loading of SLNs, during recent years. This review describes development of SLNs, the methods of preparation, characterization, and loaded drugs into SLNs in parasitic diseases. In addition, we summarize recent development in anti-parasitic SLNs-loaded drugs.

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开发用于寄生虫病的固体脂质纳米颗粒药物。
寄生虫引起的疾病症状广泛,从轻微到严重不等,是世界上大量疾病爆发的罪魁祸首。目前的抗寄生虫药物具有毒性和严重的副作用。纳米载体被认为可以消除传统药物的局限性,减少副作用,增加靶向递送和药物渗透性,控制药物的长期释放。固体脂质纳米颗粒(SLNs)是一种脂质纳米颗粒(LNPs),已被广泛应用。合适的释放速率、稳定性和靶向递送使 SLNs 成为胶体载体的良好替代品。SLNs 被认为在递送具有抗寄生虫特性的天然产品方面具有巨大潜力。近年来,人们利用纳米颗粒来提高 SLNs 的稳定性和负载能力。本综述介绍了 SLNs 的开发、制备方法、表征以及在 SLNs 中装载药物治疗寄生虫病的情况。此外,我们还总结了载入 SLN 的抗寄生虫药物的最新发展。
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