Visualization study on solid-core encapsulation behaviors of double emulsion in a flow-focusing microchannel

2019 ◽  
Vol 25 (11) ◽  
pp. 4143-4150
Author(s):  
Wei Gao ◽  
Meimei Sun ◽  
Weibo Yang ◽  
Chengbin Zhang
2020 ◽  
Vol 895 ◽  
Author(s):  
Ningning Wang ◽  
Ciro Semprebon ◽  
Haihu Liu ◽  
Chuhua Zhang ◽  
Halim Kusumaatmaja


RSC Advances ◽  
2014 ◽  
Vol 4 (37) ◽  
pp. 19061-19067 ◽  
Author(s):  
Christopher Carrick ◽  
Per A. Larsson ◽  
Hjalmar Brismar ◽  
Cyrus Aidun ◽  
Lars Wågberg

Schematic illustration of the formation of a regenerated cellulose capsule from a double emulsion using microfluidic flow focusing and isopropanol as precipitating solvent.


2016 ◽  
Vol 7 (1) ◽  
Author(s):  
Siddharth Deshpande ◽  
Yaron Caspi ◽  
Anna E. C. Meijering ◽  
Cees Dekker

Abstract Liposomes are versatile supramolecular assemblies widely used in basic and applied sciences. Here we present a novel microfluidics-based method, octanol-assisted liposome assembly (OLA), to form monodisperse, cell-sized (5–20 μm), unilamellar liposomes with excellent encapsulation efficiency. Akin to bubble blowing, an inner aqueous phase and a surrounding lipid-carrying 1-octanol phase is pinched off by outer fluid streams. Such hydrodynamic flow focusing results in double-emulsion droplets that spontaneously develop a side-connected 1-octanol pocket. Owing to interfacial energy minimization, the pocket splits off to yield fully assembled solvent-free liposomes within minutes. This solves the long-standing fundamental problem of prolonged presence of residual oil in the liposome bilayer. We demonstrate the unilamellarity of liposomes with functional α-haemolysin protein pores in the membrane and validate the biocompatibility by inner leaflet localization of bacterial divisome proteins (FtsZ and ZipA). OLA offers a versatile platform for future analytical tools, delivery systems, nanoreactors and synthetic cells.


Polymers ◽  
2019 ◽  
Vol 11 (11) ◽  
pp. 1887 ◽  
Author(s):  
Alexander Jans ◽  
Jonas Lölsberg ◽  
Abdolrahman Omidinia-Anarkoli ◽  
Robin Viermann ◽  
Martin Möller ◽  
...  

Double emulsions are useful geometries as templates for core-shell particles, hollow sphere capsules, and for the production of biomedical delivery vehicles. In microfluidics, two approaches are currently being pursued for the preparation of microfluidic double emulsion devices. The first approach utilizes soft lithography, where many identical double-flow-focusing channel geometries are produced in a hydrophobic silicone matrix. This technique requires selective surface modification of the respective channel sections to facilitate alternating wetting conditions of the channel walls to obtain monodisperse double emulsion droplets. The second technique relies on tapered glass capillaries, which are coaxially aligned, so that double emulsions are produced after flow focusing of two co-flowing streams. This technique does not require surface modification of the capillaries, as only the continuous phase is in contact with the emulsifying orifice; however, these devices cannot be fabricated in a reproducible manner, which results in polydisperse double emulsion droplets, if these capillary devices were to be parallelized. Here, we present 3D printing as a means to generate four identical and parallelized capillary device architectures, which produce monodisperse double emulsions with droplet diameters in the range of 500 µm. We demonstrate high throughput synthesis of W/O/W and O/W/O double emulsions, without the need for time-consuming surface treatment of the 3D printed microfluidic device architecture. Finally, we show that we can apply this device platform to generate hollow sphere microgels.


2016 ◽  
Vol 28 (3) ◽  
pp. 032005 ◽  
Author(s):  
Milad Azarmanesh ◽  
Mousa Farhadi ◽  
Pooya Azizian

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