Lipid nanoparticles often contain a phosphatidylcholine with a long chain fatty acid, 1,2-distearoyl--3-phosphocholine (DSPC). However, their preparation often encounters difficulties such as the inability to yield <20 nm nanoparticles due to the aggregation-prone behavior of DSPC. High-density lipoproteins (HDLs) are ∼10 nm protein-bound lipid nanoparticles in our body, and microfluidic preparations of HDL-mimicking nanoparticles (μHDL) have been reported. Herein, we report a new microfluidic mixing mode that enables preparation of μHDL with DSPC in high yield (≥90% on a protein basis). The critical mechanism of this mode is a spontaneous asymmetric distribution of the ethanol flow injected in a symmetric manner followed by turbulent mixing in a simple rectangular parallelepiped-shaped chip.
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http://dx.doi.org/10.1039/d3lc01077e | DOI Listing |
Lab Chip
June 2024
Graduate School or Engineering, Toyama Prefectural University, Imizu, Toyama, 939-0398, Japan.
Lipid nanoparticles often contain a phosphatidylcholine with a long chain fatty acid, 1,2-distearoyl--3-phosphocholine (DSPC). However, their preparation often encounters difficulties such as the inability to yield <20 nm nanoparticles due to the aggregation-prone behavior of DSPC. High-density lipoproteins (HDLs) are ∼10 nm protein-bound lipid nanoparticles in our body, and microfluidic preparations of HDL-mimicking nanoparticles (μHDL) have been reported.
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