Petit Institute for Bioengineering and Biosciences, Georgia Institute of Technology, Atlanta, GA, 30332, USA.
Department of Chemical Engineering, Georgia Institute of Technology, Atlanta, GA, 30332, USA.
Adv Healthc Mater. 2024 Jul;13(17):e2304033. doi: 10.1002/adhm.202304033. Epub 2024 Mar 10.
Poly(ethylene glycol) (PEG)-lipids are used in Food-and-Drug-Administration-approved lipid nanoparticle (LNP)-RNA drugs, which are safe and effective. However, it is reported that PEG-lipids may also contribute to accelerated blood clearance and rare cases of hypersensitivity; this highlights the utility of exploring PEG-lipid alternatives. Here, it is shown that LNPs containing poly(2-ethyl-2-oxazoline) (PEOZ)-lipids can deliver messenger RNA (mRNA) to multiple cell types in mice inside and outside the liver. In addition, it is reported that LNPs formulated with PEOZ-lipids show reduced clearance from the bloodstream and lower levels of antistealth lipid immunoglobulin Ms than LNPs formulated with PEG-lipids. These data justify further exploration of PEOZ-lipids as alternatives to PEG-lipids in LNP-RNA formulations.
聚乙二醇(PEG)脂质被用于食品和药物管理局批准的脂质纳米颗粒(LNP)-RNA 药物中,这些药物既安全又有效。然而,据报道,PEG 脂质也可能导致加速血液清除和罕见的过敏反应;这凸显了探索 PEG 脂质替代品的实用性。在这里,研究表明,含有聚(2-乙基-2-恶唑啉)(PEOZ)脂质的 LNP 可以将信使 RNA(mRNA)递送到肝脏内外的多种细胞类型。此外,据报道,与含有 PEG 脂质的 LNP 相比,用 PEOZ 脂质配制的 LNP 从血液中清除的速度较慢,抗隐匿脂质免疫球蛋白 Ms 的水平也较低。这些数据证明了 PEOZ 脂质作为 LNP-RNA 制剂中 PEG 脂质替代品的进一步探索是合理的。