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- W3198225268 abstract "Microfluidic-based synthesis is a powerful technique to prepare well-defined homogenous nanoparticles (NPs). However, the mechanisms defining NP properties, especially size evolution in a microchannel, are not fully understood. Herein, microfluidic and bulk syntheses of riboflavin (RF)-targeted poly(lactic-co-glycolic acid)-poly(ethylene glycol) (PLGA-PEG-RF) micelles were evaluated experimentally and computationally. Using molecular dynamics (MD), a conventional “random” model for bulk self-assembly of PLGA-PEG-RF was simulated and a conceptual “interface” mechanism was proposed for the microfluidic self-assembly at an atomic scale. The simulation results were in agreement with the observed experimental outcomes. NPs produced by microfluidics were smaller than those prepared by the bulk method. The computational approach suggested that the size-determining factor in microfluidics is the boundary of solvents in the entrance region of the microchannel, explaining the size difference between the two experimental methods. Therefore, this computational approach can be a powerful tool to gain a deeper understanding and optimize NP synthesis." @default.
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- W3198225268 date "2021-08-30" @default.
- W3198225268 modified "2023-10-12" @default.
- W3198225268 title "Experimental and Computational Study on the Microfluidic Control of Micellar Nanocarrier Properties" @default.
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- W3198225268 doi "https://doi.org/10.1021/acsomega.1c02651" @default.
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