2010
DOI: 10.1038/pj.2009.301
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Spontaneous extrusion of porous amphiphilic triblock copolymeric microfibers under microfluidic conditions

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Cited by 9 publications
(8 citation statements)
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“…Solvent exchange is another common method for fabricating porous microfibers. ,, Typically, an inner polymer solution (the core solution) is introduced into an outer nonsolvent liquid (the sheath solution) to form a continuous liquid jet. The contact between the two liquids induces diffusion-controlled mass transfer between the core and sheath solutions. Solvent exchange leads to polymer precipitation, which solidifies the core liquid jets into porous polymeric microfibers.…”
Section: Tailoring Wettability Of Microfibers From Liquid Jetsmentioning
confidence: 99%
“…Solvent exchange is another common method for fabricating porous microfibers. ,, Typically, an inner polymer solution (the core solution) is introduced into an outer nonsolvent liquid (the sheath solution) to form a continuous liquid jet. The contact between the two liquids induces diffusion-controlled mass transfer between the core and sheath solutions. Solvent exchange leads to polymer precipitation, which solidifies the core liquid jets into porous polymeric microfibers.…”
Section: Tailoring Wettability Of Microfibers From Liquid Jetsmentioning
confidence: 99%
“…[28] Furthermore, the drug-eluting fiber can be made out of suspension by electrospinning, [193] wet spinning, [194] or microfluidic spinning. [195][196][197] In wet spinning and microfluidic spinning, encapsulation efficiency dramatically depends on the type of antisolvent used to regenerate and solidify the fibers as it might lead to partial dissolution of the drug. [106,194,195] Wu et al [198] fabricated microfibers made of polyacrylonitrile (PAN) encapsulated with curcumin and vitamin E acetate.…”
Section: Encapsulationmentioning
confidence: 99%
“…The drug has to be administered less frequently to the patient because of the sustained release of the drug . This sustained release resembles the flat portion of the separate plots depicted in Figure (b) . The release rates and the time at which the release rate plateaus out depend on the drug molecule, the concentration of the drug molecule in the fiber, and the nature of the fiber itself. , Luu et al incorporated DNA into a fibrous scaffold made by PLGA and PLA–PEG block copolymers.…”
Section: Electrospinningmentioning
confidence: 99%
“…(a) A schematic depicting the burst-effect in a zero order controlled drug delivery . (b) The release profiles of protein and dye in DMSO (dimethyl sulfoxide) and dichloromethane from microfluidically fabricated fibers . (c) The release profiles of tetracycline hydrochloride (TCH) from electrospun TH-1/PLGA, TH-2/PLGA, tetracycline hydrochloride loaded/poly­(lactic- co -glycolic acid) composite (TCH/PLGA) nanofibers, and tetracycline hydrochloride loaded halloysite nanotubes (TCH/HNT) fibers .…”
Section: Electrospinningmentioning
confidence: 99%