School of Science, College of Science, Engineering and Health , RMIT University , Melbourne , Victoria 3000 , Australia.
CSIRO Manufacturing , Clayton , Victoria 3168 , Australia.
ACS Nano. 2019 Jun 25;13(6):6178-6206. doi: 10.1021/acsnano.8b07961. Epub 2019 May 22.
Nonlamellar lyotropic liquid crystalline (LLC) lipid nanomaterials have emerged as a promising class of advanced materials for the next generation of nanomedicine, comprising mainly of amphiphilic lipids and functional additives self-assembling into two- and three-dimensional, inverse hexagonal, and cubic nanostructures. In particular, the lyotropic liquid crystalline lipid nanoparticles (LCNPs) have received great interest as nanocarriers for a variety of hydrophobic and hydrophilic small molecule drugs, peptides, proteins, siRNAs, DNAs, and imaging agents. Within this space, there has been a tremendous amount of effort over the last two decades elucidating the self-assembly behavior and structure-function relationship of natural and synthetic lipid-based drug delivery vehicles in vitro, yet successful clinical translation remains sparse due to the lack of understanding of these materials in biological bodies. This review provides an overview of (1) the benefits and advantages of using LCNPs as drug delivery nanocarriers, (2) design principles for making LCNPs with desirable functionalities for drug delivery applications, (3) current understanding of the LLC material-biology interface illustrated by more than 50 in vivo, preclinical studies, and (4) current patenting and translation activities in a pharmaceutical context. Together with our perspectives and expert opinions, we anticipate that this review will guide future studies in developing LCNP-based drug delivery nanocarriers with the objective of translating them into a key player among nanoparticle platforms comprising the next generation of nanomedicine for disease therapy and diagnosis.
非层状溶致液晶(LLC)脂质纳米材料作为下一代纳米医学的一类有前途的先进材料而出现,主要由两亲脂质和功能添加剂自组装成二维和三维、反六方和立方纳米结构组成。特别是,溶致液晶脂质纳米颗粒(LCNP)作为各种疏水性和亲水性小分子药物、肽、蛋白质、siRNA、DNA 和成像剂的纳米载体受到了极大的关注。在这个领域,过去二十年中,人们已经付出了巨大的努力来阐明天然和合成基于脂质的药物传递载体在体外的自组装行为和结构-功能关系,但由于对这些材料在生物体内的缺乏了解,成功的临床转化仍然很少。本综述提供了(1)使用 LCNP 作为药物传递纳米载体的益处和优势,(2)设计具有理想药物传递应用功能的 LCNP 的原则,(3)通过 50 多项体内、临床前研究阐明 LLC 材料-生物学界面的当前理解,以及(4)在药物背景下的当前专利和转化活动。结合我们的观点和专家意见,我们预计本综述将指导未来基于 LCNP 的药物传递纳米载体的开发研究,旨在将其转化为下一代纳米医学中包含的纳米颗粒平台的关键参与者,用于疾病治疗和诊断。