The phospholipid composition of artificial lipid droplets enhances their deliverability and facilitates a broad Biodistribution in vivo and in vitro.

Z Telikani, I Amarasinghe, V Impicciche, A Nalbantlar, J Whan, K Caracciolo, J I Phillips, J L Dutton, L A Wallace, A Jamal, T A Gibson Hughes, K S Okuda, A Mechler, E A Monson, K J Helbig
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Abstract

Artificial lipid droplets (aLDs) provide a useful tool to explore the multiple functionalities of intracellular lipid droplets (LDs). In this study we explored the dynamics and potential multidisciplinary applications of these lipid particles. We have optimised construction of fluorescently labelled aLDs to allow their tracking in various in vitro and in vivo models. Modifying the phospholipid membrane of aLDs achieved enhanced delivery efficiency to a broad range of cells with various origins leading to a wide biodistribution of aLDs to organ systems in both mice and zebrafish models. The broad targeting and stability of this new generation of aLDs holds promise to now utilise aLDs as a novel delivery system as well as offering a toolset for further investigation on intracellular LD dynamics and function. STATEMENT OF SIGNIFICANCE: Artificial lipid droplets (aLDs) are a novel nanoparticle tool for biomedical research, consisting of a phospholipid monolayer with a neutral core interior. They offer new opportunities for the delivery of lipids and proteins in vivo; however, the ability of aLD lipid composition to drive enhanced cellular delivery remains unexplored. Here, we demonstrate that enhancing aLD phospholipid complexity significantly increases in vitro cellular delivery across multiple cell types and offers broad organ biodistribution, including delivery to the brain, in both mice and zebrafish. These findings highlight aLDs as potential vehicles in both basic biological studies and therapeutic interventions. Additionally, increasing the complexity of phospholipids into alternate nanoparticles such as LNPs may enhance organ biodistribution, thus opening the field up to new opportunities for cargo to reach previously undeliverable areas.

人工脂滴的磷脂组成提高了它们的输送能力,促进了体内和体外的广泛生物分布。
人工脂滴(ald)为探索细胞内脂滴(ld)的多种功能提供了有用的工具。在这项研究中,我们探讨了这些脂质颗粒的动力学和潜在的多学科应用。我们优化了荧光标记ald的构建,以允许它们在各种体外和体内模型中进行跟踪。在小鼠和斑马鱼模型中,通过修饰磷脂膜,可提高对多种来源细胞的递送效率,从而使ald在器官系统中广泛分布。这种新一代ald的广泛靶向性和稳定性使其有望成为一种新的递送系统,并为进一步研究细胞内LD动力学和功能提供工具集。意义声明:人工脂滴(ald)是一种用于生物医学研究的新型纳米颗粒工具,由具有中性内核内部的磷脂单层组成。它们为体内脂质和蛋白质的输送提供了新的机会;然而,aLD脂质组成驱动增强细胞递送的能力仍未被探索。在这里,我们证明了增强aLD磷脂复杂性显著增加了多种细胞类型的体外细胞递送,并在小鼠和斑马鱼中提供了广泛的器官生物分布,包括递送到大脑。这些发现突出表明,在基础生物学研究和治疗干预中,ald都是潜在的载体。此外,将磷脂的复杂性增加到替代纳米颗粒(如LNPs)中可能会增强器官的生物分布,从而为货物到达以前无法交付的区域开辟了新的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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