Crystals from charged colloids and emulsion droplets

2005 ◽  
Vol 131 ◽  
pp. 367-367
Author(s):  
P. Chaikin
2000 ◽  
Vol 10 (PR5) ◽  
pp. Pr5-109-Pr5-112
Author(s):  
J.-F. Dufrêche ◽  
J.-P. Simonin ◽  
P. Turq

Lab on a Chip ◽  
2021 ◽  
Author(s):  
Junxia Wang ◽  
Yuyu Tan ◽  
Jiajun Ling ◽  
Mingxia Zhang ◽  
Liang Li ◽  
...  

The double monoclonal display (dm-Display) has realized highly efficient monoclonal ligand screening, which can accelerate the whole process from weeks to 24 h with clone characterization throughput 1000-time higher than that of traditional approach.


Micromachines ◽  
2021 ◽  
Vol 12 (6) ◽  
pp. 723
Author(s):  
He Xia ◽  
Ang Li ◽  
Jia Man ◽  
Jianyong Li ◽  
Jianfeng Li

In this work, we used a co-flow microfluidic device with an injection and a collection tube to generate droplets with different layers due to phase separation. The phase separation system consisted of poly(ethylene glycol) diacrylate 700 (PEGDA 700), PEGDA 250, and sodium alginate aqueous solution. When the mixture droplets formed in the outer phase, PEGDA 700 in the droplets would transfer into the outer aqueous solution, while PEGDA 250 still stayed in the initial droplet, breaking the miscibility equilibrium of the mixture and triggering the phase separation. As the phase separation proceeded, new cores emerged in the droplets, gradually forming the second and third layers. Emulsion droplets with different layers were polymerized under ultraviolet (UV) irradiation at different stages of phase separation to obtain microspheres. Microspheres with different layers showed various release behaviors in simulated gastric fluid (SGF) and simulated intestinal fluid (SIF). The release rate decreased with the increase in the number of layers, which showed a potential application in sustained drug release.


Soft Matter ◽  
2021 ◽  
Author(s):  
Peng Bao ◽  
Daniel A. Paterson ◽  
Sally A. Peyman ◽  
J. Cliff Jones ◽  
Jonathan A. T. Sandoe ◽  
...  

We describe a modified microfluidic method for making Giant Unilamellar Vesicles (GUVs) via water/octanol-lipid/water double emulsion droplets and encapsulation of nematic lyotropic liquid crystals (LNLCs).


2015 ◽  
Vol 91 (3) ◽  
Author(s):  
Toshimitsu Kanai ◽  
Niels Boon ◽  
Peter J. Lu ◽  
Eli Sloutskin ◽  
Andrew B. Schofield ◽  
...  

2017 ◽  
Vol 1 (3) ◽  
pp. 507-511 ◽  
Author(s):  
Jiangping Xu ◽  
Yi Yang ◽  
Ke Wang ◽  
Yuqing Wu ◽  
Jintao Zhu

With the addition of small molecules to emulsion droplets containing block copolymers, anisotropic convex lens-like particles with hexagonally stacked cylindrical domains can be readily achieved by using a single surfactant to create a neutral interface for both blocks.


2017 ◽  
Vol 7 (4) ◽  
pp. 20160124 ◽  
Author(s):  
Keith M. Bromley ◽  
Cait E. MacPhee

Emulsions are a central component of many modern formulations in food, pharmaceuticals, agrichemicals and personal care products. The droplets in these formulations are limited to being spherical as a consequence of the interfacial tension between the dispersed phase and continuous phase. The ability to control emulsion droplet morphology and stabilize non-spherical droplets would enable the modification of emulsion properties such as stability, substrate binding, delivery rate and rheology. One way of controlling droplet microstructure is to apply an elastic film around the droplet to prevent it from relaxing into a sphere. We have previously shown that BslA, an interfacial protein produced by the bacterial genus Bacillus , forms an elastic film when exposed to an oil- or air–water interface. Here, we highlight BslA's ability to stabilize anisotropic emulsion droplets. First, we show that BslA is capable of arresting dynamic emulsification processes leading to emulsions with variable morphologies depending on the conditions and emulsification technique applied. We then show that frozen emulsion droplets can be manipulated to induce partial coalescence. The structure of the partially coalesced droplets is retained after melting, but only when there is sufficient free BslA in the continuous phase. That the fidelity of replication can be tuned by adjusting the amount of free BslA in solution suggests that freezing BslA-stabilized droplets disrupts the BslA film. Finally, we use BslA's ability to preserve emulsion droplet structural integrity throughout the melting process to design emulsion droplets with a chosen shape and size.


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