2013
DOI: 10.1016/j.biomaterials.2013.08.006
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A device for the rapid transfer/transplantation of living cell sheets with the absence of cell damage

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Cited by 35 publications
(18 citation statements)
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“…multiblock copolymer structure) and the thickness of grafted PNIPAAm immobilized covalently onto TCPS (Elloumi‐Hannachi et al ., ), inducing temperature alterations of hydrophilic/hydrophobic properties and cell adhesion/detachment (Akiyama et al ., ; Yamato et al ., ; Yamato et al ., ). So far, many articles have also reported disadvantages of NIPAAm‐grafted dishes regarding biocompatibility, low mechanical properties and lack of flexibility (Hinds et al ., ; Tadakuma et al ., ). Investigation of functional thermoresponsive hydrogels as supports for cell sheet production have gained interest for their ease of handling, inexpensive synthetic process, ease of functionalization and drug‐release ability, representing a promising alternative to NIPAAm‐grafted dishes (Martins et al ., ; Fujita et al ., ).…”
Section: Introductionmentioning
confidence: 99%
“…multiblock copolymer structure) and the thickness of grafted PNIPAAm immobilized covalently onto TCPS (Elloumi‐Hannachi et al ., ), inducing temperature alterations of hydrophilic/hydrophobic properties and cell adhesion/detachment (Akiyama et al ., ; Yamato et al ., ; Yamato et al ., ). So far, many articles have also reported disadvantages of NIPAAm‐grafted dishes regarding biocompatibility, low mechanical properties and lack of flexibility (Hinds et al ., ; Tadakuma et al ., ). Investigation of functional thermoresponsive hydrogels as supports for cell sheet production have gained interest for their ease of handling, inexpensive synthetic process, ease of functionalization and drug‐release ability, representing a promising alternative to NIPAAm‐grafted dishes (Martins et al ., ; Fujita et al ., ).…”
Section: Introductionmentioning
confidence: 99%
“…10 Most recently, a cell sheet transfer device has been developed, which has a scooping part to transfer cell sheets by a movable belt and a handling part to operate the device. 11 However, all of these methods require applying a direct force on the cell sheet, which may affect cell viability, activities, long-term functions and cause variation between users.…”
Section: Introductionmentioning
confidence: 99%
“…The cell culturing of mouse skeletal myoblast cell line C2C12 was performed as described elsewhere [16]. Briefly, Dulbecco's modified Eagle's Medium (DMEM) (A6429; Sigma-Aldrich, St. Louis, MO) supplemented with 10v/v% fetal bovine serum (FBS) (Nichirei Biosciences, Tokyo, Japan) and 1v/v% penicillin-streptomycin solution (168-23191; Wako Pure Chemical, Osaka, Japan) was prepared as a culture medium.…”
Section: Cell Culturingmentioning
confidence: 99%