Maeki Masatoshi, Kimura Niko, Okada Yuto, Shimizu Kazuki, Shibata Kana, Miyazaki Yusuke, Ishida Akihiko, Yonezawa Kento, Shimizu Nobutaka, Shinoda Wataru, Tokeshi Manabu
Division of Applied Chemistry, Faculty of Engineering, Hokkaido University Kita 13 Nishi 8, Kita-ku Sapporo 060-8628 Japan
JST PRESTO 4-1-8 Honcho, Kawaguchi Saitama 332-0012 Japan.
Nanoscale Adv. 2024 Mar 25;6(8):2166-2176. doi: 10.1039/d3na01073b. eCollection 2024 Apr 16.
Lipid nanoparticles (LNPs) are essential carrier particles in drug delivery systems, particularly in ribonucleic acid delivery. In preparing lipid-based nanoparticles, microfluidic-based ethanol injection may produce precisely size-controlled nanoparticles. Ethanol is critical in LNP formation and post-treatment processes and affects liposome size, structure, lamellarity, and drug-loading efficiency. However, the effects of time-dependent changes in the ethanol concentration on the structural dynamics of liposomes are not clearly understood. Herein, we investigated ethanol-induced lipid bilayer changes in liposomes on a time scale from microseconds to tens of seconds using a microfluidic-based small-angle X-ray scattering (SAXS) measurement system coupled with molecular dynamics (MD) simulations. The time-resolved SAXS measurement system revealed that single unilamellar liposomes were converted to multilamellar liposomes within 0.8 s of contact with ethanol, and the -spacing was decreased from 6.1 (w/o ethanol) to 4.4 nm (80% ethanol) with increasing ethanol concentration. We conducted 1 μs MD simulations to understand the molecular-level structural changes in the liposomes. The MD simulations revealed that the changes in the lamellar structure caused by ethanol at the molecular level could explain the structural changes in the liposomes observed time-resolved SAXS. Therefore, the post-treatment process to remove residual ethanol is critical in liposome formation.
脂质纳米颗粒(LNPs)是药物递送系统中的重要载体颗粒,尤其是在核糖核酸递送方面。在制备基于脂质的纳米颗粒时,基于微流体的乙醇注入法可能会产生尺寸精确可控的纳米颗粒。乙醇在LNP的形成和后处理过程中至关重要,会影响脂质体的大小、结构、片层性和载药效率。然而,乙醇浓度随时间的变化对脂质体结构动力学的影响尚不清楚。在此,我们使用基于微流体的小角X射线散射(SAXS)测量系统结合分子动力学(MD)模拟,研究了乙醇在微秒到数十秒的时间尺度上引起的脂质体脂质双分子层变化。时间分辨SAXS测量系统显示,单层脂质体在与乙醇接触的0.8秒内转变为多层脂质体,并且随着乙醇浓度的增加,层间距从6.1纳米(无乙醇时)减小到4.4纳米(80%乙醇时)。我们进行了1微秒的MD模拟,以了解脂质体在分子水平上的结构变化。MD模拟表明,乙醇在分子水平上引起的片层结构变化可以解释时间分辨SAXS观察到的脂质体结构变化。因此,去除残留乙醇的后处理过程在脂质体形成中至关重要。