Rapid quality evaluation of lipid nanoparticles using a monolithic HPLC column

The quality assurance of lipid nanoparticles (LNPs) is important for the effectiveness and safety of drugs. We developed a simple high-performance liquid chromatography (HPLC) method for rapid quality assessment of LNPs. LNPs prepared by a microchemical process were analyzed using a Tris gradient mobile phase and a poly-Lys–modified monolith as the stationary phase. This analysis produced two peaks at ~ 1 and 5 min. The fractions were collected and examined for particle morphology and zeta potential. The 1-min peak contained 20–40 nm nanoparticles, while the 5-min peak corresponded to LNPs. We applied this method to evaluate LNP stability after dilution with Tris buffer and exposure to 100 mM Ca²⁺. LNPs degraded within 1 day in Ca²⁺ at 4 °C, but > 85% remained intact after 3 days in a 500-fold Tris buffer dilution. This method enables LNP analysis within 10 min and provides a useful tool for LNP quality control.

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Publication Details

Journal
AAPS Open
Published
2026-03-02
DOI
https://doi.org/10.1186/s41120-025-00144-0
Primary Topic
Lipid Membrane Structure and Behavior
Type
article
Field-Weighted Citation Impact
0.00

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article

Rapid quality evaluation of lipid nanoparticles using a monolithic HPLC column

Manabu Tokeshi, Masatoshi Maeki, Shuhei Murayama, Masaru Kato et al.
AAPS Open
Lipid Membrane Structure and Behavior
article

Rapid quality evaluation of lipid nanoparticles using a monolithic HPLC column

Manabu Tokeshi, Masatoshi Maeki, Shuhei Murayama, Masaru Kato, Shota Miyazaki, Yukino Innami, Takashi Takaki, Nozomi Murayama, Eiichi Yamamoto, Yuki Nakatani, Masanori Motokawa
article en

Abstract

The quality assurance of lipid nanoparticles (LNPs) is important for the effectiveness and safety of drugs. We developed a simple high-performance liquid chromatography (HPLC) method for rapid quality assessment of LNPs. LNPs prepared by a microchemical process were analyzed using a Tris gradient mobile phase and a poly-Lys–modified monolith as the stationary phase. This analysis produced two peaks at ~ 1 and 5 min. The fractions were collected and examined for particle morphology and zeta potential. The 1-min peak contained 20–40 nm nanoparticles, while the 5-min peak corresponded to LNPs. We applied this method to evaluate LNP stability after dilution with Tris buffer and exposure to 100 mM Ca²⁺. LNPs degraded within 1 day in Ca²⁺ at 4 °C, but > 85% remained intact after 3 days in a 500-fold Tris buffer dilution. This method enables LNP analysis within 10 min and provides a useful tool for LNP quality control.

AAPS OpenVol. 12(1)
SHOWA Medical University (JP), Hokkaido University (JP), Saitama Prefecture (JP), National Institute of Health Sciences (JP)
Japan Agency for Medical Research and Development, Japan Society for the Promotion of Science
Openalex Percentile: Top 38%
Lipid Membrane Structure and Behavior
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