2011
DOI: 10.1002/adhm.201100020
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Multicomponent Fibers by Multi‐interfacial Polyelectrolyte Complexation

Abstract: In multi‐interfacial polyelectrolyte complexation (MIPC), fusion of nascent fibers from multiple interfaces brings the interfaces to a point from which a composite fiber is drawn. MIPC applied to two, three, and four polyelectrolyte complex interfaces leads to various patterned multicomponent fibers. Cells encapsulated in these fibers exhibit migration, aggregation and spreading in relation to the initial cell or matrix pattern.

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Cited by 55 publications
(44 citation statements)
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“…Micro/nanoscaled fibres have recently gained attention for tissue engineering approaches due to their promising potential for constructing three-dimensional structures that can be utilized as carriers for bioactive factors, drugs, and cells (Ostrovidov, Shi, et al, 2014;Tamayol, Wong, & Bahrami, 2012). Cell-loaded microfibres can simulate the hierarchical assembly of natural tissues and have been bioengineered to mimic several tissues, including cardiac, neural, muscular, and skin tissues (Jun, Kang, Chae, & Lee, 2014;Tamayol et al, 2015;Wan, Leong, Toh, et al, 2012). Thus, Onoe et al (2013) fabricated a cell-laden microfibre encapsulating primary pancreatic islet cells that was transplanted into the subrenal capsular space of diabetic mice and induced the normalization of the blood glucose concentrations post transplantation.…”
Section: Discussionmentioning
confidence: 99%
“…Micro/nanoscaled fibres have recently gained attention for tissue engineering approaches due to their promising potential for constructing three-dimensional structures that can be utilized as carriers for bioactive factors, drugs, and cells (Ostrovidov, Shi, et al, 2014;Tamayol, Wong, & Bahrami, 2012). Cell-loaded microfibres can simulate the hierarchical assembly of natural tissues and have been bioengineered to mimic several tissues, including cardiac, neural, muscular, and skin tissues (Jun, Kang, Chae, & Lee, 2014;Tamayol et al, 2015;Wan, Leong, Toh, et al, 2012). Thus, Onoe et al (2013) fabricated a cell-laden microfibre encapsulating primary pancreatic islet cells that was transplanted into the subrenal capsular space of diabetic mice and induced the normalization of the blood glucose concentrations post transplantation.…”
Section: Discussionmentioning
confidence: 99%
“…Sang‐Hoon Lee et al have adopted a coaxial flow microfluidic device to fabricate NaA‐CS microfibers; however, the filtering procedure, which is to remove undesired aggregated suspension of NaA and CS before spinning, makes the amount of CS component left in the NaA‐CS microfibers uncertain. Wan et al have used interfacial complexation technique to fabricate NaA/CS solid microfibers; however, the diameter of the microfibers fabricated by this method was varied from 10 to 20 μm. Large‐scale cells encapsulation and bulk production of the microfibers remain a bottleneck.…”
Section: Introductionmentioning
confidence: 99%
“…This combination of characteristics have been recognized as beneficial for preparation of fibers for biomedical applications. [44][45][46][47] As an additional benefit, large scale high throughput IPC spinning has been demonstrated to be feasible. [48][49][50] While IPC spinning of colloidal materials such as carbon nanotubes and protein amyloids into strong fibers has been shown, [49][50][51] IPC spinning of CNF-based fibers remains yet to be demonstrated.…”
Section: Introductionmentioning
confidence: 99%