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Microfluidic Flow-Focusing for Size-Controlled Formation of Cubosomes

Ferreira, Celso J.O. LU ; Barros, Margarida ; Fornasier, Marco LU orcid ; Chícharo, Alexandre ; Botelho, Claudia ; Real Oliveira, Maria Elisabete C.D. ; Olsson, Ulf LU orcid and Silva, Bruno F.B. (2025) In Langmuir 41(42). p.28434-28446
Abstract

Cubosomes─colloidal dispersions of lipid inverted bicontinuous cubic phases─are promising nanosystems for advanced drug delivery applications. Here, we report on a microfluidic hydrodynamic flow-focusing approach for solvent exchange that enables the preparation of cubosomes with tunable size. The approach involves a preliminary step where the lipid phytantriol, the main building block, is first dissolved in ethanol to create a precursor solution. This precursor is subsequently flowed through the central channel of a cross-shaped microfluidic device, where it is focused by two lateral streams of water containing the stabilizer Pluronic F127. As water and ethanol mix, the polarity shift forces phytantriol to self-assemble into cubosomes,... (More)

Cubosomes─colloidal dispersions of lipid inverted bicontinuous cubic phases─are promising nanosystems for advanced drug delivery applications. Here, we report on a microfluidic hydrodynamic flow-focusing approach for solvent exchange that enables the preparation of cubosomes with tunable size. The approach involves a preliminary step where the lipid phytantriol, the main building block, is first dissolved in ethanol to create a precursor solution. This precursor is subsequently flowed through the central channel of a cross-shaped microfluidic device, where it is focused by two lateral streams of water containing the stabilizer Pluronic F127. As water and ethanol mix, the polarity shift forces phytantriol to self-assemble into cubosomes, while the laminar-flow conditions imposed by the microchannels provide controlled mixing conditions. By adjusting the flow rate ratio (QR) between the water-F127 side streams and the phytantriol-ethanol precursor, we control the width of the precursor stream─the region through which solvent molecules exchange. This manipulation thus directly governs the mixing time, influencing the kinetics of lipid self-assembly, which ultimately determines particle size. This technique allows for the tuning of cubosome sizes from 195 nm down to 125 nm, with size decreasing monotonically as QRincreases and the polydispersity index remaining in the low-to-moderate range. Although variability is still significant, largely due to pumping instability and the use of a commercial microfluidic device not specifically designed for this application, the trends are statistically significant for every precursor-concentration series (p ≤ 0.011). Further customization of the apparatus is expected to improve reproducibility and scalability. The results obtained with this microfluidic method differ markedly from those obtained by bulk solvent exchange, which shows only a weak and generally nonsignificant trend toward larger particle size at higher dilution ratios.

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author
; ; ; ; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Langmuir
volume
41
issue
42
pages
13 pages
publisher
The American Chemical Society (ACS)
external identifiers
  • pmid:41105095
  • scopus:105019967181
ISSN
0743-7463
DOI
10.1021/acs.langmuir.5c03488
language
English
LU publication?
yes
additional info
Publisher Copyright: © 2025 The Authors. Published by American Chemical Society
id
4a78d7c4-e240-45ee-8e11-5bebe7d53d21
date added to LUP
2025-12-17 11:04:41
date last changed
2025-12-19 15:10:57
@article{4a78d7c4-e240-45ee-8e11-5bebe7d53d21,
  abstract     = {{<p>Cubosomes─colloidal dispersions of lipid inverted bicontinuous cubic phases─are promising nanosystems for advanced drug delivery applications. Here, we report on a microfluidic hydrodynamic flow-focusing approach for solvent exchange that enables the preparation of cubosomes with tunable size. The approach involves a preliminary step where the lipid phytantriol, the main building block, is first dissolved in ethanol to create a precursor solution. This precursor is subsequently flowed through the central channel of a cross-shaped microfluidic device, where it is focused by two lateral streams of water containing the stabilizer Pluronic F127. As water and ethanol mix, the polarity shift forces phytantriol to self-assemble into cubosomes, while the laminar-flow conditions imposed by the microchannels provide controlled mixing conditions. By adjusting the flow rate ratio (Q<sub>R</sub>) between the water-F127 side streams and the phytantriol-ethanol precursor, we control the width of the precursor stream─the region through which solvent molecules exchange. This manipulation thus directly governs the mixing time, influencing the kinetics of lipid self-assembly, which ultimately determines particle size. This technique allows for the tuning of cubosome sizes from 195 nm down to 125 nm, with size decreasing monotonically as Q<sub>R</sub>increases and the polydispersity index remaining in the low-to-moderate range. Although variability is still significant, largely due to pumping instability and the use of a commercial microfluidic device not specifically designed for this application, the trends are statistically significant for every precursor-concentration series (p ≤ 0.011). Further customization of the apparatus is expected to improve reproducibility and scalability. The results obtained with this microfluidic method differ markedly from those obtained by bulk solvent exchange, which shows only a weak and generally nonsignificant trend toward larger particle size at higher dilution ratios.</p>}},
  author       = {{Ferreira, Celso J.O. and Barros, Margarida and Fornasier, Marco and Chícharo, Alexandre and Botelho, Claudia and Real Oliveira, Maria Elisabete C.D. and Olsson, Ulf and Silva, Bruno F.B.}},
  issn         = {{0743-7463}},
  language     = {{eng}},
  month        = {{10}},
  number       = {{42}},
  pages        = {{28434--28446}},
  publisher    = {{The American Chemical Society (ACS)}},
  series       = {{Langmuir}},
  title        = {{Microfluidic Flow-Focusing for Size-Controlled Formation of Cubosomes}},
  url          = {{http://dx.doi.org/10.1021/acs.langmuir.5c03488}},
  doi          = {{10.1021/acs.langmuir.5c03488}},
  volume       = {{41}},
  year         = {{2025}},
}