2018
DOI: 10.1007/s13233-019-7013-8
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Interfacial Compression-Dependent Merging of Two Miscible Microdroplets in an Asymmetric Cross-Junction for In Situ Microgel Formation

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Cited by 10 publications
(4 citation statements)
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“…To evaluate the viability of encapsulated cells, the cells were fluorescently labeled with calcein-AM and ethidium homodimer-1 to distinguish live (green) and red (dead) cells, respectively (LIVE/DEAD Cell Viability/Cytotoxicity Kit, Thermo Fisher) [ 44 ]. The cells were visualized under a fluorescence microscope (XDS-3FL, Optika).…”
Section: Methodsmentioning
confidence: 99%
“…To evaluate the viability of encapsulated cells, the cells were fluorescently labeled with calcein-AM and ethidium homodimer-1 to distinguish live (green) and red (dead) cells, respectively (LIVE/DEAD Cell Viability/Cytotoxicity Kit, Thermo Fisher) [ 44 ]. The cells were visualized under a fluorescence microscope (XDS-3FL, Optika).…”
Section: Methodsmentioning
confidence: 99%
“…2. A wider segment is also added just after the second dispersed phase channel to facilitate droplet merging [42][43][44].…”
Section: Designmentioning
confidence: 99%
“…Jang et al [52] proposed a new in situ crosslinking methodology for the fabrication of microgels by merging two droplets of different viscosities in an asymmetric cross-junction microfluidic device. Thus, oxidized dextran (ODX) and N-carboxymethyl chitosan (N-CEC) were mixed to undergo an in situ crosslinking via a Schiff base reaction, resulting in microgel formation.…”
Section: Chitosanmentioning
confidence: 99%