TY - JOUR
T1 - Parametric Study of the Factors Influencing Liposome Physicochemical Characteristics in a Periodic Disturbance Mixer
AU - López, Rubén R.
AU - Ocampo, Ixchel
AU - Font De Rubinat, Paula G.
AU - Sánchez, Luz María
AU - Alazzam, Anas
AU - Tsering, Thupten
AU - Bergeron, Karl F.
AU - Camacho-Léon, Sergio
AU - Burnier, Julia V.
AU - Mounier, Catherine
AU - Stiharu, Ion
AU - Nerguizian, Vahé
N1 - Funding Information:
This work was supported by the grant CONACyT-ETS/389081, CONACyT International Mobility Scholarship/859557, Concordia University, NSERC/REN253, École de technologie supérieure, Khalifa University/CIRA-2019-014, and UQAM. We want to thank D. Flipo from the biological science department at UQAM for his valuable help and support in taking and processing confocal images. Also, we would like to acknowledge the group CREER, especially J. Décarie, for giving us access to Poly-Grames in cloud computing for the numerical models. CMC Microsystems supported this work through lending equipment and software. Nanoparticle Tracking Analysis was performed in collaboration with Dr. Rak and Dr. Burnier Laboratory at McGill University under the supervision of L. Montermini and T. Tsering. Prasun Lala from SARA Group ÉTS helped to proofread this article. Finally, we would like to acknowledge the chemical department at UQAM, the NanoQAM, and COFAMIQ network for the training in the cleanroom, nanoparticle characterization, and equipment use, especially to R. Izquierdo, A. Robichaud, G. Shul, J. Hue Tieu, and L. Arsenault.
Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/7/20
Y1 - 2021/7/20
N2 - Liposomes encapsulate different substances ranging from drugs to genes. Control over the average size and size distribution of these nanoparticles is vital for biomedical applications since these characteristics determine to a high degree where liposomes will accumulate in the human body. Micromixers enable the continuous flow synthesis of liposomes, improving size control and reproducibility. Recently, Dean flow dynamics-based micromixers, such as the periodic disturbance mixer (PDM), have been shown to produce controlled-size liposomes in a scalable and reproducible way. However, contrary to micromixers based on molecular diffusion or chaotic advection, their production factors and their influence over liposome properties have not yet been addressed thoroughly. In this work, we present a comprehensive parametric study of the effects of flow conditions and molecular changing factors such as concentration, lipid type, and temperature on the physicochemical characteristics of liposomes. Numerical models and confocal images are used to quantitatively and qualitatively evaluate mixing performance under different liposome production conditions and their relationship with vesicle properties. The total flow rate (TFR) and, to a lesser extent, the flow rate ratio (FRR) control the liposome size and size distribution. Effects on liposome size are also observed by changing the molecular factors. Moreover, the liposome ζ potential is independent of the factors studied here. The micromixer presented in this work enables the production of liposomes as small as 24 nm, with monodispersed to low or close to low polydispersed liposome populations as well as a production rate as high as 41 mg/h.
AB - Liposomes encapsulate different substances ranging from drugs to genes. Control over the average size and size distribution of these nanoparticles is vital for biomedical applications since these characteristics determine to a high degree where liposomes will accumulate in the human body. Micromixers enable the continuous flow synthesis of liposomes, improving size control and reproducibility. Recently, Dean flow dynamics-based micromixers, such as the periodic disturbance mixer (PDM), have been shown to produce controlled-size liposomes in a scalable and reproducible way. However, contrary to micromixers based on molecular diffusion or chaotic advection, their production factors and their influence over liposome properties have not yet been addressed thoroughly. In this work, we present a comprehensive parametric study of the effects of flow conditions and molecular changing factors such as concentration, lipid type, and temperature on the physicochemical characteristics of liposomes. Numerical models and confocal images are used to quantitatively and qualitatively evaluate mixing performance under different liposome production conditions and their relationship with vesicle properties. The total flow rate (TFR) and, to a lesser extent, the flow rate ratio (FRR) control the liposome size and size distribution. Effects on liposome size are also observed by changing the molecular factors. Moreover, the liposome ζ potential is independent of the factors studied here. The micromixer presented in this work enables the production of liposomes as small as 24 nm, with monodispersed to low or close to low polydispersed liposome populations as well as a production rate as high as 41 mg/h.
UR - http://www.scopus.com/inward/record.url?scp=85111292135&partnerID=8YFLogxK
U2 - 10.1021/acs.langmuir.1c01005
DO - 10.1021/acs.langmuir.1c01005
M3 - Article
C2 - 34232664
AN - SCOPUS:85111292135
SN - 0743-7463
VL - 37
SP - 8544
EP - 8556
JO - Langmuir
JF - Langmuir
IS - 28
ER -