Microfluidic approaches for producing lipid-based nanoparticles for drug delivery applications

IF 2.9 Q2 BIOPHYSICS
Caterina Piunti, Elisa Cimetta
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Abstract

The importance of drug delivery for disease treatment is supported by a vast literature and increasing ongoing clinical studies. Several categories of nano-based drug delivery systems have been considered in recent years, among which lipid-based nanomedicines, both artificial and cell-derived, remain the most approved. The best artificial systems in terms of biocompatibility and low toxicity are liposomes, as they are composed of phospholipids and cholesterol, the main components of cell membranes. Extracellular vesicles—biological nanoparticles released from cells—while resembling liposomes in size, shape, and structure, have a more complex composition with up to hundreds of different types of lipids, proteins, and carbohydrates in their membranes, as well as an internal cargo. Although nanoparticle technologies have revolutionized drug delivery by enabling passive and active targeting, increased stability, improved solubilization capacity, and reduced dose and adverse effects, the clinical translation remains challenging due to manufacturing limitations such as laborious and time-consuming procedures and high batch-to-batch variability. A sea change occurred when microfluidic strategies were employed, offering advantages in terms of precise particle handling, simplified workflows, higher sensitivity and specificity, and good reproducibility and stability over bulk methods. This review examines scientific advances in the microfluidics-mediated production of lipid-based nanoparticles for therapeutic applications. We will discuss the preparation of liposomes using both hydrodynamic focusing of microfluidic flow and mixing by herringbone and staggered baffle micromixers. Then, an overview on microfluidic approaches for producing extracellular vesicles and extracellular vesicles-mimetics for therapeutic applications will describe microfluidic extrusion, surface engineering, sonication, electroporation, nanoporation, and mixing. Finally, we will outline the challenges, opportunities, and future directions of microfluidic investigation of lipid-based nanoparticles in the clinic.
用于药物递送应用的脂基纳米颗粒的微流控方法
大量文献和越来越多正在进行的临床研究支持药物递送对疾病治疗的重要性。近年来,人们考虑了几种基于纳米的药物传递系统,其中基于脂质的纳米药物,无论是人造的还是细胞衍生的,仍然是最被批准的。就生物相容性和低毒性而言,脂质体是最好的人工系统,因为它们由细胞膜的主要成分磷脂和胆固醇组成。细胞外囊泡——从细胞中释放出来的生物纳米颗粒——虽然在大小、形状和结构上与脂质体相似,但其膜中含有多达数百种不同类型的脂质、蛋白质和碳水化合物,以及内部货物,其组成更为复杂。虽然纳米颗粒技术通过实现被动和主动靶向、增加稳定性、提高增溶能力、减少剂量和不良反应,彻底改变了药物输送,但由于制造限制,如费力和耗时的程序以及批次间的高可变性,临床转化仍然具有挑战性。当采用微流体策略时,发生了翻天覆地的变化,与散装方法相比,它在精确的颗粒处理、简化的工作流程、更高的灵敏度和特异性以及良好的重复性和稳定性方面具有优势。本文综述了用于治疗应用的微流体介导的脂基纳米颗粒生产的科学进展。我们将讨论利用微流体动力学聚焦和人字形和交错挡板微混合器混合制备脂质体。然后,概述了用于生产细胞外囊泡和用于治疗应用的细胞外囊泡模拟物的微流控方法,将描述微流控挤出、表面工程、超声、电穿孔、纳米穿孔和混合。最后,我们将概述脂基纳米颗粒在临床微流体研究中的挑战、机遇和未来方向。
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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CiteScore
3.60
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0.00%
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