2018
DOI: 10.1016/j.ejpb.2018.02.024
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Fabrication of antibody-loaded microgels using microfluidics and thiol-ene photoclick chemistry

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Cited by 21 publications
(22 citation statements)
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“…However, microgels possess unique properties of both hydrogels and colloidal particles, such as structural integrity, compartmentalization, orthogonal functionalization, softness, deformability, permeability, stimuli-responsiveness, reversible swelling, and adaptivity, and have been found to be promising for a wide range of applications in various fields including controlled drug release, separation technology, bio-, and chemical sensors, etc. [312][313][314][315][316][317][318][319][320][321][322][323][324][325][326] Microgels can be fabricated mainly via emulsion polymerization with an added surfactant, surfactant-free emulsion polymerization (SFEP), inverse mini-, and microemulsion polymerization, as well as the crosslinking of prepolymer chains, etc. [327,328] Typically, the techniques used to break-up and gel the particles for microgel formation will determine the final microgel properties, including the structure, size, and strength [329] and the presence and amount of crosslinks determine the "colloidal" or "macromolecular" character of the microgel.…”
Section: Microgelsmentioning
confidence: 99%
“…However, microgels possess unique properties of both hydrogels and colloidal particles, such as structural integrity, compartmentalization, orthogonal functionalization, softness, deformability, permeability, stimuli-responsiveness, reversible swelling, and adaptivity, and have been found to be promising for a wide range of applications in various fields including controlled drug release, separation technology, bio-, and chemical sensors, etc. [312][313][314][315][316][317][318][319][320][321][322][323][324][325][326] Microgels can be fabricated mainly via emulsion polymerization with an added surfactant, surfactant-free emulsion polymerization (SFEP), inverse mini-, and microemulsion polymerization, as well as the crosslinking of prepolymer chains, etc. [327,328] Typically, the techniques used to break-up and gel the particles for microgel formation will determine the final microgel properties, including the structure, size, and strength [329] and the presence and amount of crosslinks determine the "colloidal" or "macromolecular" character of the microgel.…”
Section: Microgelsmentioning
confidence: 99%
“…Visible light photoinitiation is advantageous for the encapsulation of biological materials as UV radiation can cause DNA damage and accelerate tissue aging and cancer onset. Blue light photo-initiators that can be used are camphorquinone [ 82 ], eosin Y [ 83 ], and riboflavin [ 84 , 85 ].…”
Section: Microfluidic Production Of Spherical Matrix-type Microgelsmentioning
confidence: 99%
“…Visible light photoinitiation is advantageous for encapsulation of biological materials since UV radiation can cause DNA damage and accelerate tissue aging and cancer onset. Blue light photo-initiators that can be used are camphorquinone [77], eosin Y [78], and riboflavin [79,80].…”
Section: Photopolymerisationmentioning
confidence: 99%
“…Water soluble pre-polymers modified by introduction of cross-linkable molecules can be used instead of monomers. The examples of such modified polymers used for microfluidic production of microgels are dextran-hydroxyethyl methacrylate (dextran-HEMA) [85], gelatin-methacryloyl (GelMA) [86,87], poly(N-isopropylacrylamide-dimethylmaleimide), (P(NIPAAm-DMMI)) [88], poly(ethylene glycol diacrylate) (PEGDA) [89], poly(ethylene glycol methyl ether acrylate) (PEGMA) [90], poly(ethylene glycol) norbornene (PEG-NB) [78], and 6-armed acrylated PEG [91].…”
Section: Photopolymerisationmentioning
confidence: 99%