Future Industries Institute and ARC Centre of Excellence Convergent Bio-Nano Science and Technology, University of South Australia, Mawson Lakes Campus, Adelaide, SA 5095, Australia.
UniSA Clinical and Health Science and ARC Centre of Excellence Convergent Bio-Nano Science and Technology, University of South Australia, City West Campus, Adelaide, SA 5000, Australia.
Int J Pharm. 2021 Apr 1;598:120391. doi: 10.1016/j.ijpharm.2021.120391. Epub 2021 Feb 20.
The mucus covering of epithelial tissues presents one significant biological barrier to the uptake and absorption of particulate carriers. Improved understanding of the mechanisms mediating the transport of nanoparticles across such mucus layers would accelerate their development as optimised mucosal drug delivery formulations (e.g. via oral and rectal routes). Herein, an in vitro mucus model ("Mucus-on-Chip") was developed to enable the interaction and transport of functionalised nanoparticles and reconstituted mucus to be quantitatively investigated in real-time. We verified that the diffusion of nanoparticles into mucus is highly dependent on their biointerfacial properties. Muco-inert modification (PEGylation) significantly enhanced the mucopenetration of 50 nm and 200 nm nanoparticles, whereas limited mucopenetration was observed for pectin coated mucoadhesive nanoparticles. Furthermore, this model can be easily adapted to mimic specific physiological mucus environments. Mucus pre-treated with a mucolytic agent displayed reduced barrier function and therefore significantly accelerated mucopenetration of nanoparticles, which was independent of their size and biointerfacial properties. This new "Mucus-on-Chip" methodology provides detailed insight into the dynamics of nanoparticle-mucus interaction, which can be applied to refine the design of particulate formulations for more efficient mucosal drug delivery.
上皮组织的黏液覆盖层对颗粒载体的摄取和吸收构成了一个重要的生物学屏障。深入了解介导纳米颗粒穿过此类黏液层的转运机制,将加速它们作为优化的黏膜给药制剂(例如通过口服和直肠途径)的发展。在此,开发了一种体外黏液模型(“芯片上黏液”),以实时定量研究功能化纳米颗粒和重建黏液的相互作用和转运。我们验证了纳米颗粒扩散进入黏液高度依赖于它们的生物界面特性。亲脂性修饰(PEG 化)显著增强了 50nm 和 200nm 纳米颗粒的黏液穿透性,而果胶涂层的黏附性纳米颗粒的黏液穿透性有限。此外,该模型可以很容易地适应模拟特定的生理黏液环境。用黏液溶解剂预处理的黏液显示出降低的屏障功能,因此显著加速了纳米颗粒的黏液穿透性,这与它们的大小和生物界面特性无关。这种新的“芯片上黏液”方法提供了对纳米颗粒-黏液相互作用动力学的详细了解,可用于改进颗粒制剂的设计,以实现更有效的黏膜药物传递。